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| Pharma Exec’s Top 50 Pharma Companies 2015 |
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| Specialty drug sales, record-breaking M&A paired with tax synergies, and global expansion helped to bring a new face into this year’s Pharma 50 top 10, and substantially boosted the rankings of several others. |
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| 5 Tips to Help Your FDA 510(k) Submission |
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| Jon Speer, founder of greenlight.guru, is an expert at getting medical devices to market. If you’re developing a medical device in the US, chances are your path to market involves a FDA 510(k) submission. Here are his tips… |
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| The 2015 BIO International Convention Closes in Philadelphia |
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| This year’s Convention hosted 29,279 partnering meetings, a new record for the event. Organized by the Biotechnology Industry Organization (BIO), the event drew 15,858 industry leaders from 69 countries and 47 states, as well as the District of Columbia and Puerto Rico. |
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Q&A: The Future of Clinical Trial Data Sharing |
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| The drive for the transparency of clinical trial data continues to build momentum. This mission is supported by Dr. Michael Rosenblatt, Executive VP and CMO at Merck & Co. Rosenblatt recently discussed this issue in an interview with Applied Clinical Trials. |
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| UDI is here: 7 Things You Need to Know |
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| Since US medical device regulators have begun implementing their Unique Device Identification (UDI) system, Emergo has identified seven key common issues to consider as you undertake UDI compliance projects. Check out the seven things you need to know. |
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