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Discussion on Raw Material Methods and Specifications
Presented By Netzealous LLC DBA - Compliance4All
Wednesday, April 4th at 10:00am PST
Online sale ends: 04/04/18 at 9:00am PST
Online
161 Mission Falls Lane, Suite 216,
Fremont, CA 94539
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Talent
Lamont M. Fulton Description
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 facility The supplier's commitment to conforming to appropriate excipient GMP requirements Characterization of the composition of the excipient. Acceptability of Standards from Alternative Compendia (BP/EP/JP) Who Will Benefit: Quality Assurance/Control Product Development/Formulator/R&D Chemist Analytical Chemist/QC Lab Regulatory Affairs Material Management Speaker 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$150.00 Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com http://www.compliance4all.com/control/w_product/~product_id=501795LIVE?channel=purplepass_Apr_2018_SEO Additional Information
One Dial-in One Attendee
Price: $150.00
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Presented By
10:00am to 11:00am
General Admission: $150.00
50 18004479407 UPCOMING EVENTS
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