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ONLINE WEBINAR 2017 - CMO Supplier Quality Agreements - How to Comply with New FDA and EU Guidelines for Contract Drug Manufacturing

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Category Quality Agreement, Contract Manufacturing, Pharmaceutical, Drug, FDA, EU, GMP, Contracted Facility, quality issues with CMOs, Contract Manufacturing Organisation, assurance of GMP compliance, lab controls, sub-contracting, facilities and equipment, GMP responsibilities.

Deadline: April 10, 2017 | Date: April 11, 2017

Venue/Country: CA, U.S.A

Updated: 2017-03-20 18:16:07 (GMT+9)

Call For Papers - CFP

This webinar will provide a thorough understanding of the content that is expected in Quality Agreements from a regulatory perspective.

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.