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Latest News | 17 May 2013

FDA Finalizes Guidance on Priority Review Process for Medical Devices

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Capping off a week of several long-awaited guidance documents, the US Food and Drug Administration's (FDA) Center for Devices and Radiological Health (CDRH) has released yet another guidance document, Read More...


Latest News | 17 May 2013

US Would See Clinical Trials Reporting Transparency Under New Legislation

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Massachusetts U.S. Rep. Ed Markey has announced the reintroduction of legislation that he says is intended to open up clinical trial data, introducing a measure of transparency and bringing the US Read More...


Latest News | 17 May 2013

EMA Releases ICH Guideline on Manufacturing Impurities for Industry Consultation

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The European Medicines Agency (EMA) has announced its adoption of the International Conference on Harmonisation's (ICH) M7 guideline on controlling carcinogenic risk in pharmaceutical products when Read More...


Regulatory Update | 17 May 2013

EU’s Scientific Committees to Look at Synthetic Biology

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The European Commission’s three Scientific Committees have been requested to provide a joint scientific opinion on the relationship of Synthetic Biology (SB) to genetic modification of organisms, its Read More...


Latest News | 17 May 2013

Pharmaceutical Industry to FDA: Build Flexibility into GAIN Act

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When legislators passed a sprawling piece of legislation known as the Food and Drug Administration Safety and Innovation Act (FDASIA), they considered a huge range of problems facing both the US Food Read More...


Latest News | 17 May 2013

FDA Data Show the Worst is Over for 510(k), PMA Submissions

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The medical device industry has long complained that the process of obtaining regulatory approval for its devices has become increasingly difficult over the course of the last decade. But in a Read More...


Latest News | 17 May 2013

Regulatory Reconnaissance (17 May 2013)

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Welcome to Regulatory Reconnaissance, your daily regulatory news and intelligence briefing.In Focus: US Is the Hatch-Waxman Act Flawed and Should the Supreme Court Fix It? (Becker's Hospital Read More...


Latest News | 16 May 2013

Janssen's Simponi Wins New Indication for Treatment of Ulcerative Colitis

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The US Food and Drug Administration (FDA) has announced the approval of additional indications for Simponi (golimumab), a drug manufactured by Janssen Biotech intended to treat adults with moderate to Read More...


Latest News | 16 May 2013

NIH Looks to Drug Reformulation, Social Media to Combat Opioid Abuse and Misuse

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The US Food and Drug Administration (FDA) may be at the forefront of trying to prevent the misuse and abuse of opioid painkillers, but as two Federal Register notices this week point out, it's not the Read More...


Latest News | 16 May 2013

Is FDA Approving Too Many Drugs Starting with 'X' and 'Z'?

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Regulators with the US Food and Drug Administration (FDA) had a few things to clarify with industry and medical practitioners in the latest issue of the New England Journal of Medicine.Namely: No, Read More...


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RF Today is Regulatory Focus' daily news brief. Each edition contains the top global regulatory news stories about pharmaceuticals, medical devices, biotechnology and more. Learn more

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