07.09.14 -- Transcept And Paratek Sign Merger Agreement; FDA Grants Priority Review To Boehringer Ingelheim's Nintedanib NDA
November 10 and 11, 2014 | Hyatt Regency, San Francisco, CA
• Who should attend? Pharma and biopharm executives who form and manage outsourcing partnerships.
• What's on the agenda? Educational sessions focused on best practices and industry leaders’ experiences and lessons learned to help you avoid costly mistakes.
Register today! Space is limited. Brought to you by Life Science Leader magazine, BayBio, and Outsourced Pharma.
Digging For Big Data Gold: Data Mining As A Route To Drug Development Success By Suzanne Elvidge, Contributing Editor
Big Data is becoming a major part of all facets of healthcare as more and more clinical trials results and other drug development and approval documents are being stored electronically. The challenge of Big Data is the number of combinations and factors involved, which is where data mining comes to the rescue.
White Paper: The Trend In Global Sourcing By Brian Kohr, President and CEO, CSafe
Global sourcing is a 'business-essential' that continues to be of increasing importance to life sciences companies. As manufacturers adapt to changing market conditions, consolidate their operations, and focus thought leadership to work as one company across borders, continents, and markets, the drive to make cost and efficiency savings becomes ever more demanding.
White Paper: What Is FDA 21 CFR Part 11, And Are Your Systems Compliant? By Infitrak, Inc.
21 CFR Part 11 is a federal statutory provision designed to codify specific Best Practices for certain industries. Particularly, it authorizes commercial entities to establish and utilize computerized networks that exponentially enhance individual productivity levels via drastic reduction of manual data entry errors.
The Envirotainer RAP t2 container provides accurate and reliable protection for large shipments of temperature-sensitive products. The RAP is only forkliftable when empty and is most commonly handled with rollerbeds.
Marken has trained professionals on hand with global expertise to protect and manage the logistics of medical devices, diagnostic equipment, and medical components, including sensitive microchips and surgical equipment. Their expertise also extends to ECG/ABM devices, stents, pacemakers, and investigator site specimen separation devices.
Small-format AseptiQuik S Connectors from Colder Products Company extend the range of sterile fluid connectors to now include 1/8" and 1/4" flow configurations. Proven AseptiQuik technology, combined with an intuitive and robust genderless design, provides biopharmaceutical manufacturers with even greater flexibility in making sterile connections.
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