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Encision first quarter 2013 revenue decreases to $3.1 million

Encision Inc., a medical device company owning patented surgical technology that is emerging as a standard of care in minimally-invasive surgery, today announced financial results for its fiscal 2013 first quarter ended June 30, 2012.

25 Jul 2012

Where does Ryan stand on Romney's list?

NPR reports on the effect Rep. Paul Ryan, R-Wis., could have if Mitt Romney chose him as a running mate. Ryan's budget plan, which includes sweeping changes to Medicare, is one of the reasons why he may not be "the safest choice."

25 Jul 2012

Details emerge regarding personalities involved in FDA flap

An FDA scientist whose complaints about the agency's approval process for medical devices led to a controversial email monitoring program had filed lawsuits against two hospitals where he worked and also sued a dozen medical-device companies.

21 Jul 2012

Redesign of 'outdated and unsafe' medical bags can cut MRSA risk

A new medical bag designed in the UK is set to transform treatment around the world after a study found a third of its outdated predecessors carry the MRSA bug.

21 Jul 2012

Treating complex spinal pathologies: an interview with Eric Major

In the approximate $8 billion global spine market, the most specialized and demanding $1 billion complex spine segment includes deformity, trauma, and tumor pathologies.

20 Jul 2012

Mindray acquires orthopedics business of Dragonbio

Mindray Medical International Limited, a leading developer, manufacturer and marketer of medical devices worldwide, announced today the completion of its acquisition of Wuhan Dragonbio Surgical Implant's orthopedics business pursuant to the terms of the definitive agreement entered into on June 6, 2012.

From Mindray 18 Jul 2012

Grassley: FDA officials OK'd surveillance on groups of doctors wary of medical device safety

Congressional investigators said Monday that the chief counsel's office at the Food and Drug Administration authorized wide-ranging surveillance of a group of the agency's scientists, the first indication that the effort was sanctioned at the highest levels. In a letter to the FDA, Sen. Charles E. Grassley (R-Iowa) said that his staff had learned that the spying was "explicitly authorized, in writing" by the agency's top legal office.

18 Jul 2012

Johnson & Johnson second quarter sales decrease 0.7% to $16.5B

Johnson & Johnson today announced sales of $16.5 billion for the second quarter of 2012, a decrease of 0.7% as compared to the second quarter of 2011. Operational results increased 3.5% and the negative impact of currency was 4.2%.

17 Jul 2012

First Edition: July 17, 2012

Today's headlines include a report that concludes that few Americans will pay more as a result of the health law.

17 Jul 2012

Elsevier introduces PLD solution for professionals in the life sciences

Elsevier, a world-leading provider of scientific, technical, and medical information products and services, today announced the launch of a structured Product Literature Database (PLD) solution for professionals in the life sciences.

16 Jul 2012

Study examines link between phthalates and diabetes in women

A study lead by researchers from Brigham and Women's Hospital (BWH) shows an association between increased concentrations of phthalates in the body and an increased risk of diabetes in women. Phthalates are endocrine disrupting chemicals that are commonly found in personal care products such as moisturizers, nail polishes, soaps, hair sprays and perfumes.

14 Jul 2012

Quick-Med Technologies grants Derma Sciences global license to NIMBUS antimicrobial technology

Derma Sciences, Inc., a medical device and pharmaceutical company focused on advanced wound care, and Quick-Med Technologies, Inc., a life sciences company that is developing innovative technologies for the healthcare and consumer markets, announce the signing of an agreement whereby Quick-Med Technologies has granted Derma Sciences an exclusive global license to intellectual property related to the novel NIMBUS antimicrobial technology, which is available in BIOGUARD dressings.

13 Jul 2012

Longer looks: Keeping Parkinson's a secret

When Nancy Mulhearn learned she had Parkinson's disease seven years ago, she kept the diagnosis mostly to herself, hiding it from friends, colleagues -- even, at first, her mother, sister and teenage children. After seven months, she decided she had to tell her family, and they settled into an unspoken agreement not to talk about the disease.

13 Jul 2012

President Obama signs FDA bipartisan bill

President Obama signed into law the bipartisan Food and Drug Administration (FDA) Safety and Innovation Act (FDASIA) on July 9.

11 Jul 2012

Derma Sciences’ MEDIHONEY HCS dressings receive CE Mark

Derma Sciences, Inc., a medical device and pharmaceutical company focused on advanced wound care, announces receipt of the CE Mark for the Company's patented MEDIHONEY HCS (hydrogel colloidal sheet) dressings.

10 Jul 2012

Roundup: Calif. insurers to lower rate hikes for small businesses, Mass. Gov backs easing doc gift ban

Tens of thousands of small businesses in California collectively will save $48 million on their health insurance bills starting this month now that three insurers have agreed to reduce pending rate hikes.

10 Jul 2012

Novel system to treat hair loss receives CE Mark approval

Restoration Robotics, Inc., a privately-held medical device company, today announced its revolutionary ARTAS System received CE Mark Certificate to market in the European Union. The ARTAS System is the first physician controlled, computer assisted technology that allows harvesting individual follicular units directly from the scalp.

9 Jul 2012

New hemoglobin monitoring system for anemia screening introduced by OrSense Ltd.

OrSense Ltd., developer of monitors for non-invasive measurements of various blood parameters, introduced today at the 32nd International Congress of the International Society of Blood Transfusion (ISBT), in Cancun, Mexico, GlasswingTM, its next-generation, wireless, non-invasive hemoglobin (Hb) measurement system for anemia monitoring, hemorrhage detection and pre-donation screening.

9 Jul 2012

FDA proposes UDI regulations for most medical devices

Today, in response to requirements in legislation that passed Congress with broad bipartisan support, the U.S. Food and Drug Administration proposed that most medical devices distributed in the United States carry a unique device identifier, or UDI.

4 Jul 2012