Introduction to Dissolution Method Development and Validation
Website https://www.onlinecompliancepanel.com/webinar/DISSOLUTION-METHOD-DEVELOPMENT-VALIDATION-504758/AUGUS |
Edit Freely
Category Dissolution Instrument Qualification, FDA Requirements, EMA Requirements, FIP Position Paper, Mechanical Qualification, USP Performance Verification Tablets, USP 1058, USP 711, Performance Verification Test, Dissolution Method Development and Validation, Dissolution testing
Deadline: August 28, 2017 | Date: August 29, 2017
Venue/Country: U.S.A
Updated: 2017-08-16 16:46:07 (GMT+9)
Call For Papers - CFP
Learn the regulatory and compendial drivers for dissolution methods and how to develop a dissolution method for a pharmaceutical dosage form. Attend webinar.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.