Cyborg | Designer-Babies | Futurism | Futurist | Immortality | Longevity | Nanotechnology | Post-Human | Singularity | Transhuman

Apr 232013

Following a year of outstanding innovation, achievement and growth Liberty is proud to announce its rebranding.

Edmonton, AB (PRWEB) April 17, 2013

Libertys launch into the healthcare industry and developments over the past year, lead Liberty to a new mission statement that reflects the companys passion for creating opportunities for everyone connected to Liberty.

Libertys new mission is to create opportunities for its customers, employees, partners and the communities they live in. Liberty achieves this by focusing on the needs of our customers above all else. Through innovation and applying new technology, we strive to simplify and empower the lives of those who are connected to Liberty.

Libertys new look allows the freedom to build on existing health care and commercial accounts, while reflecting the increasing trend towards home automation and energy management for residential customers. Liberty has removed the word security for the familiar Liberty Security in favor of progression towards home automation, integrated systems for commercial and movement into the health care industry.

The new Liberty green represents growth, a fresh perspective and the youthful nature of our company. Libertys slogan remains Simple | Safe | Smart as Liberty is and always will be dedicated to simplified solutions for customers. Nathan Baldry founder and managing partner at Liberty says, the changes weve made to our companys brand may seem subtle on the surface, they represent our overall direction for the future.

For additional information please visit http://www.libertysecurity.ca

Call Liberty at 1.866.926.7233 or email info(at)libertysecurity(dot)ca

Alexa Morency Liberty Security Systems 780.988.7233 Email Information

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Liberty Announces its Rebranding

SANTA CRUZ DE LA PALMA, SPAIN–(Marketwired – Apr 9, 2013) – Cisco (NASDAQ: CSCO) –The council of the island of La Palma and the Canary Island Health Service announced the launch of the first telemedicine service available in Spain. This is a pioneering project based on the Cisco HealthPresence software platform, enabling patients in the General Hospital of La Palma and the University Hospital of the Canary Islands in Tenerife to obtain medical assistance remotely, without any need to travel from one island to another. This offers a time-saving benefit, convenience and the potential for economic efficiency.

Cisco and the council of the island of La Palma have been collaborating with the aim at furthering a strategy of economic development while improving the quality of life of the island’s inhabitants (Project Antares) by developing information and communication technologies.

Cisco, the University Hospital of the Canary Islands, and the General Hospital of La Palma today demonstrated the service by conducting a virtual consultation between a doctor situated in the University Hospital in Tenerife and a user in La Palma. The virtual consultation has shown all the advantages of this Cisco technology with a potential of revolutionizing health care, helping improve patient satisfaction and increasing medical efficiency.

Key points of the announcement

Statements in support

Internet of Everything (IoE)In a world of health and care, the Internet of Everything can have amazing impact when we enable and enhance the patient and caregiver experience. Care-at-a-Distance is one important example of how securely bringing together the healthcare ecosystem including people, information and devices can change the way we change the way we deliver healthcare and wellness.

Additional resources

About CiscoCisco (NASDAQ: CSCO) is the worldwide leader in IT that helps companies seize the opportunities of tomorrow by proving that amazing things can happen when you connect the previously unconnected. For ongoing news, please go to http://thenetwork.cisco.com.

Cisco and the Cisco logo are trademarks or registered trademarks of Cisco and/or its affiliates in the U.S. and other countries. A listing of Cisco’s trademarks can be found at www.cisco.com/go/trademarks. Third-party trademarks mentioned are the property of their respective owners. The use of the word partner does not imply a partnership relationship between Cisco and any other company.

RSS Feed for Cisco: http://newsroom.cisco.com/rss-feeds

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La Palma and Tenerife Islands Launch the First Telemedicine Service in Spain

HACKENSACK, N.J., March 14, 2013 (GLOBE NEWSWIRE) — Freedom Home Healthcare, New Jersey’s leading provider of private in-home care for older adults, has embarked on a year-long celebration in honor of the company’s 10th anniversary.

Freedom was founded in 2003 as Freedom Eldercare and first opened its doors in Union City, NJ. Today, Freedom serves the entire state of New Jersey from its headquarters in Hackensack, as well as two offices in Mt. Laurel and North Brunswick.

“When the founders of Freedom conceived of the innovative and unique model of home care we offer today, they could have only hoped that our clients, their families and geriatric professionals would fully embrace and appreciate the concierge level of service we bring to the industry,” said Barbra London, Freedom’s president. “As evidenced by our rapid and continuing growth, the level of appreciation for our services has only increased over the past 10 years and has exceeded every expectation.”

Throughout 2013, Freedom will offer a variety of professional events throughout the state. Plus, the company will launch a new series called “Ask the Experts” that will help educate clients and their family members regarding various elder care issues.

“Ten years later, the entire Freedom team prides itself on being a thought leader in the industry, as well as a frequent presenter at national and local professional conferences,” said London. “We are honored that more than 3,000 clients and their families have trusted us to deliver compassionate care over the past 10 years.”

For more information about Freedom’s services and locations, visit www.freedom-homehealthcare.com.

About Freedom Home Healthcare

Founded in 2003, Freedom Home Healthcare (www.freedom-homehealthcare.com) is a premier provider of in-home care for older adults, their families and professional referral sources. The company’s full spectrum of concierge-level services includes hourly, respite and live-in care, as well as long-distance caregiving and geriatric care management. With three offices located throughout New Jersey, Freedom provides both short- and long-term care.

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Freedom Home Healthcare Celebrates 10 Years of Service and Excellence

NEW YORK, Feb. 19, 2013 /PRNewswire/ — Reportlinker.com announces that a new market research report is available in its catalogue:

Regenerative medicine and Stem cells Partnering Terms and Agreements http://www.reportlinker.com/p01098514/Regenerative-medicine-and-Stem-cells-Partnering-Terms-and-Agreements.html#utm_source=prnewswire&utm_medium=pr&utm_campaign=Biological_Therapy

The Regenerative Medicine and Stem Cells Partnering Terms and Agreements report provides comprehensive understanding and unprecedented access to the Regenerative medicine and Stem cells partnering deals and agreements entered into by the worlds leading healthcare companies.

Trends in regenerative medicine and stem cells deals Deal terms analysis Partnering agreement structure Partnering contract documents Top deals by value Most active dealmakers Average deal terms for regenerative medicine and stem cells

The report provides a detailed understanding and analysis of how and why companies enter regenerative medicine and stem cells partnering deals. The majority of deals are development stage whereby the licensee obtains a right or an option right to license the licensors regenerative medicine and stem cells technology. These deals tend to be multicomponent, starting with collaborative R&D, and commercialization of outcomes.

This report provides details of the latest regenerative medicine and stem cells agreements including cell therapy agreements announced in the healthcare sector.

Understanding the flexibility of a prospective partner’s negotiated deals terms provides critical insight into the negotiation process in terms of what you can expect to achieve during the negotiation of terms. Whilst many smaller companies will be seeking details of the payments clauses, the devil is in the detail in terms of how payments are triggered contract documents provide this insight where press releases and databases do not.

This report contains a comprehensive listing of all regenerative medicine and stem cells partnering deals announced since 2008 including financial terms where available including over 550 links to online deal records as disclosed by the deal parties. In addition, where available, records include contract documents as submitted to the Securities Exchange Commission by companies and their partners.

Contract documents provide the answers to numerous questions about a prospective partner’s flexibility on a wide range of important issues, many of which will have a significant impact on each party’s ability to derive value from the deal.

For example, analyzing actual company deals and agreements allows assessment of the following:

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Regenerative medicine and Stem cells Partnering Terms and Agreements



SEO Summer Training 3/Three Months MBA/PGDM Internship Noida Ghaziabad NCR- Apex TG Google Panda.wmv
Apex Technology Group Inc www.apextgi.in Apex TG India Pvt. Ltd. http Apex TG India Pvt. Ltd. focuses on delivering sophisticated technology-enabled solutions to maximize complex business needs. Founded in 2006 and based in New Delhi; the company has provided successful solutions and services to a variety of industries, ranging from Finance, Healthcare, Pharmaceuticals to Telecommunications. The advantage of working with Apex TG India Pvt. Ltd. is our level of experience coupled with our familiarity with the market dynamics and latest technologies. For more information call or email your resume at 0120-4029000 /9953584548

By: ApexTG

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SEO Summer Training 3/Three Months MBA/PGDM Internship Noida Ghaziabad NCR- Apex TG Google Panda.wmv – Video

HACKENSACK, N.J., Jan. 31, 2013 (GLOBE NEWSWIRE) — Freedom Home Healthcare, a leading provider of geriatric care management and in-home care for older adults, announced today that it has opened a new branch in North Brunswick, NJ. The company has two additional offices in Hackensack and Mt. Laurel.

“Since 2003, Freedom has been providing in-home health care services that enable older adults to age with grace and dignity,” said Barbra London, Freedom’s president. “With our newest location in central New Jersey, we are now positioned to provide care to older adults living throughout the entire state.”

In addition to providing in-home care for older adults, Freedom also serves as an informational resource to other health care professionals. Throughout the years, the Freedom team of experts has provided continuing education seminars for social workers, nurses, long-term care administrators and assisted living administrators.

“We’re excited to call central New Jersey home and to provide older adults living in surrounding communities with the exceptional care for which we are known,” said London. “We also look forward to building relationships with local health care providers who share our commitment to excellence.”

For more information about Freedom’s services and locations, visit .freedom-homehealthcare.com.

About Freedom Home Healthcare

Founded in 2003, Freedom Home Healthcare (www.freedom-homehealthcare.com) is a premier provider of in-home care for older adults, their families and professional referral sources. The company’s full spectrum of concierge-level services includes hourly, respite and live-in care, as well as long-distance caregiving and geriatric care management. With three offices located throughout New Jersey, Freedom provides both short- and long-term care.

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Freedom Home Healthcare Opens New Branch in North Brunswick

US porn companies are battling legislation in Los Angeles that requires actors to use condoms, arguing that it is against free speech.

BBC News reports that Vivid Entertainment and Califa Productions have launched legal action in a bid to overturn the law, known as Measure B.

Measure B requires porn studios in Los Angeles County to commit to using condoms in order to receive a filming permit. It has been supported by the AIDS Healthcare Foundation as a way to reduce actors’ exposure to HIV.

In the lawsuit, the studios argue that the law “violates the guarantee of free speech in the US constitution’s First Amendment”.

Vivid Entertainment founder Steven Hirsch said that he felt the current industry HIV and STI testing system “works well”.

“Overturning this law is something I feel very passionate about,” he added.

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Porn studios argue 'free speech' in condom legal fight



We've Been Robbed of Pensions, Healthcare Free Speech in the Workplace
Just the latest casualties in the billionaire's war against the rest of us.

By: TheBigPictureRT

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We’ve Been Robbed of Pensions, Healthcare

SOUTH SAN FRANCISCO, CA–(Marketwire – Dec 3, 2012) – VistaGen Therapeutics, Inc. ( OTCBB : VSTA ), a biotechnology company applying stem cell technology for drug rescue, predictive toxicology and drug metabolism screening, has formalized its membership in the Toronto-based Centre for Commercialization of Regenerative Medicine’s (CCRM) Industry Consortium.

“VistaGen’s membership reflects our strong association with CCRM and its core programs and objectives, both directly and through our strategic relationships with Dr. Gordon Keller and the University Health Network (UHN).Our long-term sponsored research agreement with Dr. Keller, UHN and UHN’s McEwen Centre for Regenerative Medicine offers both a solid foundation and unique opportunities for expanding the commercial applications of our Human Clinical Trials in a Test Tube platform by building multi-party collaborations with CCRM and members of its Industry Consortium,” says Shawn Singh, VistaGen CEO. “These collaborations have the potential to transform medicine and accelerate significant advances in human health and wellness that stem cell technologies and regenerative medicine promise.”

“Even before VistaGen joined CCRM’s Industry Consortium it was active in the Toronto regenerative medicine community and advising us as we prepared to launch in 2011,” explains Dr. Michael May, CEO of the Centre for Commercialization of Regenerative Medicine. “I’m confident that our relationship will grow stronger with VistaGen as a formal partner and I look forward to us working closely together on projects that will accelerate drug discovery and benefit patients.”

CCRM is a not-for-profit, public-private consortium funded by the Government of Canada, six Ontario-based institutional partners and more than 20 companies representing the key sectors of the regenerative medicine industry. CCRM supports the development of foundational technologies that accelerate the commercialization of stem cell- and biomaterials-based products and therapies. Other members of CCRM’s Industry Consortium include such leading global companies as Pfizer, GE Healthcare and Lonza.

The industry leaders that comprise the CCRM consortium benefit from proprietary access to certain licensing opportunities, academic rates on fee-for-service contracts at CCRM and opportunities to participate in large collaborative projects, among other advantages.VistaGen is especially well positioned through its existing relationships with key members.

Gordon Keller, Ph.D. is Director of the McEwen Centre for Regenerative Medicine at UHN. A CCRM partner, the McEwen Centre is a world-renowned centre for stem cell biology and regenerative medicine and a world-class stem cell research facility. He is also a Professor at the University of Toronto in the Department of Medical Biophysics and Senior Scientist of the Ontario Cancer Institute in Toronto.Dr. Keller’s lab is one of the world leaders in successfully applying principles from the study of developmental biology of many animal systems to the differentiation of pluripotent stem cell systems, resulting in reproducible, high-yield production of human heart, liver, blood and vascular cells.The results and procedures developed in Dr. Keller’s lab are often quoted and used by academic scientists worldwide.

UHN, a major landmark in Canada’s healthcare system, is one of the world’s largest research hospitals, with major research in transplantation, cardiology, neurosciences, oncology, surgical innovation, infectious diseases and genomic medicine. Providing care to the community for more than two centuries, UHN brings together the talent and resources needed to achieve global impact and provide exemplary patient care, research and education.

About VistaGen Therapeutics

VistaGen is a biotechnology company applying human pluripotent stem cell technology for drug rescue, predictive toxicology and drug metabolism screening. VistaGen’s drug rescue activities combine its human pluripotent stem cell technology platform, Human Clinical Trials in a Test Tube, with modern medicinal chemistry to generate new chemical variants (Drug Rescue Variants) of once-promising small-molecule drug candidates. These are drug candidates discontinued by pharmaceutical companies, the U.S. National Institutes of Health (NIH) or university laboratories after substantial investment and development due to heart or liver toxicity or metabolism issues. VistaGen uses its pluripotent stem cell technology to generate early indications, or predictions, of how humans will ultimately respond to new drug candidates before they are ever tested in humans, bringing human biology to the front end of the drug development process.

Additionally, VistaGen’s small molecule drug candidate, AV-101, is completing Phase 1 development for treatment of neuropathic pain. Neuropathic pain, a serious and chronic condition causing pain after an injury or disease of the peripheral or central nervous system, affects millions of people worldwide.To date, VistaGen has been awarded over $8.5 million from the NIH for development of AV-101.

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VistaGen Therapeutics Becomes Member of Centre for Commercialization of Regenerative Medicine (CCRM) Consortium

Published: 8:10AM Wednesday November 07, 2012 Source: Reuters

New York mayor Michael Bloomberg speaks to the media during a news conference. – Source: Reuters

New York City ordered the evacuation of hundreds of nursing home residents today, and the closure of parks and beaches ahead of a threatening new storm, as the region struggles to recover from Superstorm Sandy’s deadly flooding and high winds.

With a strong “Nor’easter” forecast to strike the devastated area tomorrow, Mayor Michael Bloomberg said residents in the city’s lowest-lying and hardest-hit areas would also be evacuated to shelters tomorrow.

“We just don’t need to send our first responders into the ocean to save someone who is being foolish,” Bloomberg said.

Outside construction work must stop at noon Wednesday (local time), and parks and beaches will also close then for 24 hours. Bloomberg ordered the evacuation today of over 600 people from four healthcare centres in the ravaged Rockaways section of Queens.

“These four facilities are in the most heavily-impacted area of the Rockaways and have been successfully operating on generator power,” said Bloomberg. “A Nor’easter storm surge could compromise their generators, putting elderly residents at risk.”

He also said people would be evacuated from the south shore of Staten Island – home to nearly half of the 40 people killed in New York City by Sandy.

Bloomberg stressed that the evacuations, which were designed to coincide with high tides when the storm surge would be highest, would not be as widespread as the mandatory evacuations of large parts of the city before Sandy struck on October 29.

Former hurricane Sandy was a rare hybrid superstorm when it lashed the US Northeast, swamping seaside towns, flooding the New York subway and knocking out power to millions of homes. It killed at least 120 people in the United States and Canada.

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NYC parks, beaches closed as new storm approaches

NORTHRIDGE, CA and CAMBRIDGE, UNITED KINGDOM–(Marketwire – Oct 22, 2012) – Regenerative medicine companyAvita Medical Ltd. ( ASX : AVH ),( OTCQX : AVMXY ) announced that further to Australian Stock Exchange announcements on 5 September 2012 and 16 October 2012 and following today’s Shareholder Meeting it is pleased to announce the appointments of Jeremy Curnock Cook and Matt McNamara to the board of Avita Medical.The strengthening of Avita’s board follows the company’s successful capital raising of A$10.3m.

Avita Medical’s Chairman, Dalton Gooding stated the appointments of Mr Curnock Cook and Mr McNamara further strengthenAvita’s board.

“I am delighted that both Jeremy and Matt have been appointed as directors of Avita Medical and I extend a warm welcome on behalf of the board,” Mr Gooding said.

“We look forward to drawing on the extensive experience that both Jeremy and Matt have in biotechnology and healthcare as we continue to increase our ReCell SprayOn Skin sales.”

Mr Curnock Cook is currently on a number of boards of international healthcare and biotechnology companies.Jeremy is the former head of the life science private equity team at Rothschild Asset Management, was responsible for the launch of the first dedicated biotechnology fund for the Australian market and the launch of a joint venture with Johnson & Johnson Development Corporation for the creation of Healthcare Ventures, an investment vehicle dedicated to seed stage investments in Europe, as well as the conception and launch of the International Biotechnology Trust (IBT).

MrMcNamaraiscurrentlytheChiefInvestmentOfficerandFundManagerofOctaPhillip Bioscience Managers.Matt has over 23 years experience in the healthcare & medical sciences sector. After initially being a molecular biology research assistant, Matt spent 11 years in Sales & Marketing and General Management with Merck & Co. and Johnson& Johnson Medical Pty. Ltd. respectively. He has served as SVP Business Development for a University of Sydney spin out, eBioinformatics Inc., and was CEO of a Life Sciences Venture Capital fund, SciCapital Pty. Ltd.

The board would also like to thank Dr Paul Watt who has retired from the board of Avita Medical effective immediately.The board would like to acknowledge Dr Watt’s extensive contribution that he has made over a 10 year period including 6 years as a director of premerger company Visiomed Limited.Dalton Gooding stated, “The board wishes Dr Watt all the very best and success with his future endeavors.”

ABOUT AVITA MEDICAL LTD Avita Medical (http://www.avitamedical.com/) develops and distributes regenerative and tissue-engineered products for the treatment of a broad range of wounds, scars and skin defects. Avita’s patented and proprietary tissue-culture, collection and application technology provides innovative treatment solutions derived from a patient’s own skin. The company’s lead product, ReCell Spray-On Skin, is used in a wide variety of burns, plastic, reconstructive and cosmetic procedures. ReCell is patented, CE-marked for Europe, TGA-registered in Australia, and SFDA-cleared in China. ReCell is on market and generating early revenues. ReCell is not available for sale in the United States; in the U.S. ReCell is an investigational device limited by federal law to investigational use. A Phase III FDA trial is in process.

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Avita Strengthens Board

WASHINGTON, DC–(Marketwire – Oct 17, 2012) – The Alliance for Regenerative Medicine (ARM), the international organization representing the interests of the regenerative medicine community, announced the publication today of an article on FDA communications to help companies developing cell-based therapies by clarifying the development pathway. The article, entitled “Communications with the FDA on the Development Pathway for a Cell-Based Therapy: Why, What, When, and How?” will be published in the journal Stem Cells Translational Medicine. It is co-authored by representatives from ARM, Janssen R&D, GE Healthcare and Life Technologies, with the lead author from the California Institute for Regenerative Medicine (CIRM).

“There are a number of ways cell-based therapy companies can communicate with FDA that will help them navigate the road from the bench to a regulatory submission,” said Michael Werner, Executive Director of ARM. “We hope that our combined experience as co-authors, and our attempt to create a single source of guidance on the regulatory process, will help companies bring new cell-based therapies through clinical trials and the regulatory review process more quickly so they can reach patients faster,” added Mr. Werner.

Lead author Ellen Feigal, MD, Senior Vice President for Research and Development at the California Institute for Regenerative Medicine (CIRM) commented, “Cell-based therapies represent a fundamentally new way to treat or cure disease, but developing a new therapy is costly, time consuming and fraught with uncertainty. Our paper takes a practical approach to clarifying the path to market.”

“Communications with the FDA on the Development Pathway for a Cell-Based Therapy: Why, What, When, and How?” provides detailed information on options for communicating with the FDA at different stages; the official communications tied to each stage of development; and the most common reasons regulatory applications are delayed. The article can be accessed at: http://stemcellstm.alphamedpress.org/content/early/recent

About CIRM: CIRM was established in November 2004 with the passage of Proposition 71, the California Stem Cell Research and Cures Act. The statewide ballot measure, which provided $3 billion in funding for stem cell research at California universities and research institutions, was overwhelmingly approved by voters, and called for the establishment of an entity to make grants and provide loans for stem cell research, research facilities, and other vital research opportunities. A list of grants and loans awarded to date may be seen here: http://www.cirm.ca.gov/for-researchers/researchfunding.

About ARM: The Alliance for Regenerative Medicine is a Washington, DC-based multi-stakeholder advocacy organization that promotes legislative, regulatory and reimbursement initiatives necessary to facilitate access to life-giving advances in regenerative medicine. ARM also works to increase public understanding of the field and its potential to transform human healthcare, providing business development and investor outreach services to support the growth of its member companies and research organizations. Prior to the formation of ARM in 2009, there was no advocacy organization operating in Washington, DC to specifically represent the interests of the companies, research institutions, investors and patient groups that comprise the entire regenerative medicine community. Today ARM has more than 120 members and is the leading global advocacy organization in this field. In March 2012, ARM launched a sister organization in Europe — the Alliance for Advanced Therapies. For more information go to www.alliancerm.org.

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Journal Stem Cell Translational Medicine to Publish Article on FDA Communications and the Regulatory Pathway for Cell …

CLARKSTON, Mich., Oct. 16, 2012 /PRNewswire/ –Clarkston, Mich.-based Freedom One Financial Group, a 401(k) plan recordkeeping and administrative service provider, announced today that Freedom One Investment Advisors, Inc. will provide 401(k) plan advisory services for Port Huron, Mich.-based Blue Water Obstetrics & Gynecology, P.C. Freedom One Financial Group Vice President of Strategic Growth & Development Errol Hau made the announcement.

Blue Water Obstetrics & Gynecology, P.C., provides a full-spectrum of health care for women, offering knowledgeable and compassionate obstetrical care. Freedom One Financial Group will work with Blue Water Obstetrics & Gynecology, P.C., to handle the company’s retirement assets for participants.

The addition of Blue Water Obstetrics & Gynecology, P.C. to Freedom One Financial Group’s growing client roster expands upon the company’s continued storied growth in Michigan. As a Michigan-based company, the firm prides itself on partnering with other local companies within the state.

“By adding Blue Water Obstetrics & Gynecology, P.C., to our roster of Michigan-based clients we are continuing to expand our footprint in the healthcare industry, which is a critical part of the state’s economic landscape,” said Hau. “We look forward to providing them our industry-leading participant education programs, which ensure employees stay on-track for meeting their retirement goals.”

In a prepared statement, JoAnn Brooks, Office Manager of Blue Water Obstetrics & Gynecology, P.C., stated “We recently decided to upgrade our existing profit sharing plan to add a 401(k) plan. When comparing potential providers we felt that partnering with an organization that specialized in providing advisory and administrative services for qualified plans was important. Freedom One has relieved us of a significant administrative burden, has brought us into full compliance and will save me hundreds of man hours a year; all while significantly reducing our fiduciary liability by providing independent investment advisory services. The transition was quick, smooth and professional. We have reduced our annual costs while adding a 401(k) to our plan, a real win-win!”

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Blue Water Obstetrics & Gynecology, P.C., Retains Freedom One Financial Group as 401(k) Plan Advisor

MARLBOROUGH, Mass.–(BUSINESS WIRE)–

Advanced Cell Technology, Inc. (ACT; OTCBB: ACTC), a leader in the field of regenerative medicine, announced today that the Data and Safety Monitoring Board (DSMB), an independent group of medical experts closely monitoring the Companys three ongoing clinical trials, has authorized the Company to move forward with enrollment and treatment of second and third additional patients with Stargardts macular dystrophy (SMD) in the second patient cohort of its U.S. trial for the condition. Additionally, the DSMB has authorized the Company to treat all three patients in the second cohort of its European trial for SMD.

The UK Medicines and Healthcare products Regulatory Agency (MHRA) recently approved a protocol modification to the DSMB review, streamlining the process, allowing the company to treat the first patient in a new cohort if the DSMB has allowed this in the US study, and once clearance has been received in the US trial to treat the next two patients in the US cohort. This would also allow for treatment of the UK patients without an additional review by the DSMB. Moreover, according to the protocol for both trials, each patient in the second cohort will be injected with 100,000 human embryonic stem cell (hESC)-derived retinal pigment epithelial (RPE) cells, up from 50,000 in the first cohort.

This authorization to treat the next five patients in the second, higher-dosage cohort in both our clinical trials for SMD represents a significant step forward for our clinical programs, commented Gary Rabin, chairman and CEO of ACT. We are also encouraged with the MHRAs approval of the DSMBs streamlined review process. Clearly this has the potential to help accelerate the pace of our European trial.

ACT is conducting three clinical trials in the U.S. and Europe using hESC-derived RPE cells to treat forms of macular degeneration, SMD and dry age-related macular degeneration (dry AMD). Each trial will enroll a total of 12 patients, with cohorts of three patients each in an ascending dosage format, from 50,000 hESC-derived RPE cells in the first patient cohort to 200,000 in the last and final cohort. These trials are prospective, open-label studies, designed to determine the safety and tolerability of hESC-derived RPE cells following sub-retinal transplantation into patients with dry-AMD or SMD at 12 months, the studys primary endpoint.

We are eagerly anticipating treating these final two patients in the second cohort of our U.S. trial for SMD, and all three patients in the second cohort of our E.U. trial, commented Robert Lanza, M.D., ACTs chief scientific officer. We are encouraged by the preliminary data in the first patient in this second, higher-dosage cohort and look forward to gathering more data.

Further information about patient eligibility for ACTs SMD studies in the U.S. and E.U. as well as its dry AMD study are available atwww.clinicaltrials.gov,with the following Identifiers: NCT01345006 (U.S. SMD), NCT01469832 (E.U. SMD), and NCT01344993 (dry AMD).

About Advanced Cell Technology, Inc.

Advanced Cell Technology, Inc., is a biotechnology company applying cellular technology in the field of regenerative medicine. For more information, visit www.advancedcell.com.

Forward-Looking Statements

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ACT Announces Approval to Treat Additional Stargardt’s Disease Patients with Higher RPE Dosage in Both U.S. and …

TUCSON, Ariz.–(BUSINESS WIRE)–

Liberty Star Uranium & Metals Corp. (Liberty Star or the Company)(LBSR: OTCQB) is pleased to announce Pete OHeeron of Houston, Texas has joined the Liberty Star Board of Directors. Mr. OHeeron is a significantly large and longtime LBSR shareholder and was instrumental in forging a relationship between Liberty Star and Northern Dynasty Minerals, resulting in a strategic partnership and the resurgence of Liberty Star in the southwestern Alaska mining region. Mr. Charles D. Vollmer has resigned as Director to pursue his Jobenomics Movement full time. If the opportunity presents itself, Liberty Star will team with Mr. Vollmers Jobenomics on future projects.

About Mr. OHeeron:

Mr. OHeeron leads an operationalinvestmentgroup which identifies early stage opportunities in the medical field with strong intellectual property positions. Through his 20+ years of medical product development experience, Mr. OHeeron brings together the resources from strategic disciplines necessary to commercialize unique technologies. Prior to founding Advanced Medical Technologies LLC, Mr. OHeeron founded NeoSurg Technologies, Inc. to develop a minimally invasive access system. As a result of his efforts, NeoSurg Technologies was successful in developing the T2000 Minimally Invasive Access System, the world leader in reposable surgical instrumentation. Mr. OHeeron completed the sale of NeoSurg Technologies to CooperSurgical in 2005. Mr. OHeeron graduated from Texas StateUniversitywith a BS in Healthcare Administration and a minor in Business Administration. He received his Masters in Healthcare Administration from the University of Houston. Mr. OHeeron currently holds 5 patents and has 4 patents pending.

Jim Briscoe, Liberty Star CEO and Chief Geologist, comments, Petes business acumen and natural ability connecting with people will definitely stimulate our growth potential. Even before becoming a Liberty Star Director, Petes support benefitted us materially. I have found there to be a real similarity between the scientific methodology of practicing medicine and exploration geology and I especially appreciate Petes achievements in the field of medical technology; he understands what we do as mineral explorers. Pete is a very energetic entrepreneur who will introduce Liberty Star to investors that are attracted to our commitment to using cutting-edge technology in mineral exploration.

James A. Briscoe James A. Briscoe, Professional Geologist, AZ CA CEO/Chief Geologist Liberty Star Uranium & Metals Corp.

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Pete O’Heeron Named to Liberty Star Board of Directors

In the Obama campaign’s attack on the Romney-Ryan proposal to “voucherize” Medicare, one accusation is that the plan would force seniors to pay more of their healthcare costs: about $6,400 more per beneficiary, according to a recent TV ad known as “Facts.” Regardless of the “facts” in the ad, this attack takes as a given that any such outcome is undesirable.

Yet asking seniors to pay substantially more is precisely the way to improve Medicare. Here’s why.

The purpose of insurance is to protect against large, unforeseeable expenses. If everyone faces some risk of substantial health costs, but no individual can predict whether or when these will occur, everyone can benefit by pooling these risks via insurance.

This argument does not apply, however, to small or predictable expenditures. It makes no sense to buy insurance against the “risk” of routine medical care, such as annual checkups, or against the risk of moderate expenses, such as many medication regimes, minor surgeries or treatments. Homeowners insurance does not cover broken toilets or snow removal, only major events such as a fire. These expenditures may well be worthwhile. For example, annual checkups might help avoid larger medical expenses in future. But most consumers can afford these without insurance.

In addition, insurance can make the healthcare market less efficient by reducing consumer incentive to economize on health costs. This “moral hazard” is a major reason behind escalating costs. When consumers are not paying for their care, the incentives for excessive utilization are huge: unnecessary tests, too much surgery rather than watchful waiting, doctor visits with minimal value, brand name versus generic drugs and more.

The way to diminish moral hazard is with large deductibles. If the first, say, $6,400 of medical costs per year must be paid by the insured, people would economize on healthcare and shop for lower prices when care was needed. And such high-deductible policies still accomplish insurance’s main goal: protecting against catastrophic risks.

Medicare, alas, makes minimal use of deductibles (or copays, a related mechanism for reducing moral hazard). Patients are, therefore, insensitive to costs and demand ever more healthcare as technological progress yields new tests, drugs, devices, treatments and procedures. Costs therefore escalate. Insurance and the extent of coverage, not technological progress, is the culprit.

So Medicare should phase in a much higher deductible, starting now. The increase would presumably be small or zero for those already retired; somewhat higher for those nearing retirement; but gradually rise to a substantial value (e.g., $6,400) for those decades away from eligibility.

The improvement in Medicare’s finances would be huge. Assume at least 40 million elderly beneficiaries pay an increased deductible of $6,400. That would reduce Medicare expenditure by roughly $250 billion per year once fully phased in. And this does not affect the poorest elderly, who are eligible for Medicaid rather than Medicare.

This reduction in Medicare’s expenses is not the main benefit, however. Lower Medicare expenditure is just the flip side of the higher deductibles paid by seniors and therefore not a net benefit to the economy.

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Fixing Medicare requires seniors to pay quite a bit more

Current debate over the best path for reforming our healthcare system stems from a fundamental clash of ideologies. Are people and society best served by greater government involvement in a market? Or does greater economic freedom facilitate the best outcomes? Those on the side of free market solutions often point to [...]

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Economic Freedom's Impact on Healthcare, Coffee, And Garbage Collection

MAPLE GROVE, Minn., July 12, 2012 /PRNewswire/ — Rough, dry patches of skin would make Lady Liberty herself want to lower her torch-bearing arm and seek relief. Between splashing in the pool and hanging out in the AC, summertime is prime time for drying skin saboteurs. If independence from dry skin is what you seek, look no further than AmLactin Moisturizing Body Lotion. With clinically proven 12% lactic acid, it gently exfoliates and intensely hydrates, leaving behind soft skin that would make even America’s Founding Fathers proud.

“Many people think dry skin is a ‘winter thing’ and come to me with concerns when it appears in the summer,” says board certified New York cosmetic dermatologist, Dr. Doris Day. “Dry skin can occur at any time and is associated with many conditions, Keratosis Pilaris (KP) being one of them. KP is an incurable skin condition and can be worsened by extreme environmental conditions in any season. For these reasons, I recommend incorporating exfoliation into your skincare routine regardless of the weather. A moisturizer rich in alpha-hydroxys, like AmLactin Moisturizing Body Lotion, makes this important step simple. Its dual action formula contains lactic acid, which works to exfoliate away dry, dead skin while providing essential moisture to new cells underneath.”

About AmLactin Alpha-Hydroxy Skin Care AmLactin moisturizers contain alpha-hydroxy acids (AHAs), which are effective at exfoliating and hydrating the skin. AmLactin formulas also contain emollients and humectants that help retain the skin’s natural moisture and draw water to the skin so it looks and feels soft and smooth. The AmLactin Alpha-Hydroxy Skin Care line includes AmLactin Moisturizing Body Lotion, AmLactin Ultra Hydrating Body Cream for severe dry skin (formerly AmLactin XL ) and AmLactin Foot Cream.

AmLactin Ultra Hydrating Body Cream is specially formulated for severe, persistently dry skin areas that need extra attention. It contains the advanced, patented ULTRAPLEX formula that gently exfoliates and is clinically proven to intensely hydrate for long-lasting moisture. With rich humectants and creamy emollients, AmLactin Ultra provides serious relief.

When using products with AHA, be sun smart: use sunscreen, wear protective clothing, and limit sun exposure while using these products and for a week afterward.

All AmLactin products are available without a prescription at Costco, Walmart, Walgreens, CVS, Rite-Aid, www.drugstore.com and other fine retailers nationwide. For more information, a store locator and downloadable coupons, visit www.amlactin.com. For tips on managing dry skin associated with Keratosis Pilaris and to watch a video on “How Lactic Acid Works,” visit www.littleredbumps.com.

Upsher-Smith Upsher-Smith Laboratories, Inc. is a privately held, U.S.-based company devoted to improving health and advancing wellness since 1919. Upsher-Smith demonstrates its commitment to meeting the healthcare needs of its customers through developing, producing and marketing consumer and prescription products. In addition to its strong heritage in generics, Upsher-Smith’s branded businesses focus on women’s health, dermatology and CNS therapeutic areas. For additional information, visit http://www.upsher-smith.com.

Sources: Data on File. Upsher-Smith Laboratories, Inc.

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Enjoy the Freedom of Beautiful Skin: Exercise Your Right to Radiance with AmLactin® Moisturizing Body Lotion

SAN DIEGO, April 20, 2012 /PRNewswire/ –Millennium Laboratories, the leading research-based clinical diagnostic lab dedicated to improving the lives of people suffering from pain, announced today that it is pleased to be a significant sponsor of the upcoming Freedom & Recovery Conference, hosting the keynote event, “An Evening with Dakota Meyer.” The Freedom & Recovery Conference, which takes place April 23-26 at the Hotel Del Coronado in San Diego, addresses integrated mental health and addiction treatment for service members. The mental health issues covered will include psychological trauma, pain management, anxiety and depression, and life after service.

(Logo: http://photos.prnewswire.com/prnh/20120224/MM59482LOGO)

During his keynote presentation on Tuesday, April 24, U.S. Marine veteran and Medal of Honor recipient, Dakota Meyer, will share his inspiring and motivational story about his time with the Marine Corp, bring attention to the various treatment methods available to returning military men and women and raise awareness of how our military is affected by the circumstances of war and service.

Specializing in pain management, Millennium Laboratories and Millennium Research Institute understand and support the evolving complexities that the Department of Defense and the Veterans Administration are addressing with Service Members:

“Millennium Laboratories is invested in helping Service Members transition successfully back into their communities,” said Nancy Lazarski, Vice President of Global Defense Healthcare at Millennium. “We are humbled to be able to sponsor this event that supports those who have served our country, and we will continue to collaborate with organizations that help veterans navigate the emotional aspects of transitioning back into their communities and into the workplace.”

For more information about Freedom & Recovery or to attend the event, “An Evening with Dakota Meyer,” please visit the conference website: http://www.foundationsrecoverynetwork.com/events/freedom-and-recovery-2012/index.htm

About Millennium Laboratories:

Millennium Laboratories is the leading research-based clinical diagnostic company dedicated to improving the lives of people suffering from pain. The company provides healthcare professionals with scientific data, clinical tools and services that help personalize treatment plans to improve clinical outcomes and patient safety.

The company utilizes leading technology and proprietary methodologies to provide some of the fastest and most reliable medication monitoring and drug detection results via both urine drug testing (UDT) and oral fluid testing. Test results are backed by expert toxicologists, clinical guidance and dedicated customer service.

Millennium’s commitment to advancing the science and the field of pain management also includes a strong focus on the advancement of industry research, education and advocacy. Through its association with the Millennium Research Institute, a nonprofit national research center, it quickly has gained respect as a leader in toxicology, pharmacology and pain management research and education, providing healthcare professionals with innovative research to advance the assessment and management of chronic pain.

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Millennium Laboratories Sponsors 2012 Freedom & Recovery Conference and Keynote Presentation by American Hero …

HOLLISTON, Mass., March 6, 2012 (GLOBE NEWSWIRE) — Harvard Bioscience, Inc. (Nasdaq:HBIO – News), a global developer, manufacturer, and marketer of a broad range of tools to advance life science research and regenerative medicine is deeply saddened to learn of the passing of Mr. Christopher Lyles. Mr. Lyles was a recent recipient of a tracheal transplant regenerated in a Harvard Bioscience InBreath Bioreactor. Currently, we do not know the cause of Mr. Lyle’s death. Our thoughts are with his family at this time. His family has released the following statement:

“We, the family of Christopher Lyles, sorrowfully inform you that Christopher passed away this morning, March 5, 2012. Christopher was a recipient and strong advocate of stem cell therapy. We do not want his journey to be in vain. We hope his bravery will pave the way for further research and development and acceptance of stem cell based therapies in the United States. We would like to thank everyone for their thoughts and prayers throughout Christopher’s trailblazing journey.”

About Harvard Bioscience

Harvard Bioscience (“HBIO”) is a global developer, manufacturer and marketer of a broad range of specialized products, primarily apparatus and scientific instruments, used to advance life science research and regenerative medicine. We sell our products to thousands of researchers in over 100 countries primarily through our 850 page catalog (and various other specialty catalogs), our website, through distributors, including GE Healthcare, Thermo Fisher Scientific and VWR, and via our field sales organization. HBIO has sales and manufacturing operations in the United States, the United Kingdom, Sweden, Germany and Spain with additional facilities in France and Canada. For more information, please visit www.harvardbioscience.com.

The Harvard Bioscience, Inc. logo is available at http://www.globenewswire.com/newsroom/prs/?pkgid=6426

Forward-looking Statements

The statements made in this press release that are not statements of historical fact are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. You can identify these forward-looking statements by our use of such words as “will,” “guidance,” “objectives,” “optimistic,” “potential,” “future,” “expect,” “plans,” “estimates,” “continue,” “drive,” “strategy,” “crucial,” “potential,” “potentially,” “growth,” “long-term,” “projects,” “projected,” “produce,” “intends,” “believes,” “goals,” “sees,” “seek,” “develop,” “possible,” “new,” “enabling,” “emerging,” “opportunity,” “pursue” and similar expressions that do not relate to historical matters. Forward-looking statements in this press release may include, but are not limited to, statements or inferences about the HBIO’s or management’s beliefs or expectations, the field of regenerative medicine, opportunities or potential opportunities in the field of regenerative medicine, HBIO’s business strategy, the positioning of HBIO for growth, the market demand and opportunity for HBIO’s current products or products it is developing or intends to develop, and HBIO’s plans, objectives and intentions that are not historical facts.

These statements involve known and unknown risks, uncertainties and other factors that may cause HBIO’s actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. Factors that may cause HBIO’s actual results, performance or achievements to differ materially from those in the forward-looking statements include, but are not limited to, HBIO’s failure to successfully expand its product offerings, introduce new products or commercialize new technologies, including in the field of regenerative medicine, decreased demand for the HBIO’s products, including products in the field of regenerative medicine, due to changes in our customers’ needs, our ability to obtain regulatory approvals, including FDA approval, for our products, including any products in the field of regenerative medicine, the current size or anticipated size of the regenerative medicine market, the existence and size of opportunities in the regenerative medicine market, our financial position, plus risk factors set forth under the heading “Item 1A. Risk Factors” in HBIO’s Annual Report on Form 10-K for the fiscal year ended December 31, 2010 or described in HBIO’s other public filings. HBIO’s results may also be affected by factors of which HBIO is not currently aware. HBIO may not update these forward-looking statements, even though its situation may change in the future, unless it has obligations under the federal securities laws to update and disclose material developments related to previously disclosed information.

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Harvard Bioscience Comments on the Passing of Christopher Lyles



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