ONLINE WEBINAR 2016 - Introduction to Dissolution Method Development & Validation
Website http://onlinecompliancepanel.com/webinar/DISSOLUTION-VALIDATION-501478/JUNE-2016-ES-OURGLOCAL |
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Category Dissolution Method Development, Analytical Target Profile, Validation, Trending, Analytical Procedure, Immediate Release, Extended Release, USP Dissolution Apparatus, Drug Products, U S Pharmacopeia Reference Standards, USP, Drug Development, Developing Dissolution Method, Scale-up and Post-Approval Changes Guidance, SUPAC, SUPAC Guidance, FDA Guidelines, Food and Drug Administration, FDA Guidance, Risk Management, Quality Assurance, Quality Management, Biowaivers, Bioequivalence Studies, Pharmaceutical Industry, Pharma, Drug Development, Quality Control, Pharma Test, Dissolution Test, Drug Approval Process
Deadline: June 02, 2016 | Date: June 03, 2016
Venue/Country: Fremont, U.S.A
Updated: 2016-05-05 19:27:08 (GMT+9)
Call For Papers - CFP
Register for this webinar and learn the dissolution testing method lifecycle concept, its requirements in analytical target profile, method design and development for the drug products.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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