Discussion on Raw Material Methods and Specifications
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Website http://www.compliance4all.com/control/w_product/~product_id=501795LIVE?channel=ourglocal_Apr_2018_SE |
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Category Healthcare trainings, medical trainings, food health, healthy courses
Deadline: April 03, 2018 | Date: April 04, 2018
Venue/Country: Online, U.S.A
Updated: 2018-02-20 14:00:31 (GMT+9)
Call For Papers - CFP
Overview:Based on knowledge of the active and inactive ingredient's function and role in the finished dosage form, Compendia methods and specifications are clearly accepted by third parties and regulatory agencies.Why should you Attend:The FDA has Approved hundreds of inactive ingredients for thousands of products with various dosage forms (routes of administration). The quantities and quality of each inactive ingredient is critical to the function and design of the final product formulation.Areas Covered in the Session:Description of the API and excipient manufacturing process and facilityThe supplier's commitment to conforming to appropriate excipient GMP requirementsCharacterization of the composition of the excipient.Acceptability of Standards from Alternative Compendia (BP/EP/JP)Who Will Benefit:Quality Assurance/ControlProduct Development/Formulator/R&D ChemistAnalytical Chemist/QC LabRegulatory AffairsMaterial ManagementSpeaker Profile: Mr. Lamont Michael Fulton is President of Regulatory Direction LLc and has over Forty years of Pharmaceutical experience (26 in regulatory affairs CMC).He has had roles as both Manager and Director of Chemistry Manufacturing and Controls (CMC) Regulatory and labeling at both Branded (Merck, SmithKline, Wyeth) and Generic drugs firm (Mylan). Event Fee: One Dial-in One Attendee Price: US$150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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