Auditing API Facilities: A MUST to properly prepare for an FDA Regulatory API GMP Inspection
Website https://www.complianceonline.com/auditing-active-pharmaceutical-ingredient-facilities-webinar-traini |
Edit Freely
Category
Deadline: May 15, 2019 | Date: May 15, 2019
Venue/Country: U.S.A
Updated: 2019-04-09 03:05:20 (GMT+9)
Call For Papers - CFP
In this FDA inspection webinar attendees will learn the basic understanding of Active Pharmaceutical Ingredient Good Manufacturing Practices (ICH Q7) and the most important elements of API GMP to avoid serious deviations and failures during either a Pre-Approval or GMP Inspection.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.