Apr, 04

Discussion on Raw Material Methods and Specifications

Wednesday, Apr, 04, 2018 From 10:00 AM to 11:00 AM

LOCATION
Fremont, CA, USA

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* Note : This is a public Event.

Discussion on Raw Material Methods and Specifications

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

venue

Fremont, CA, USA

Buy Tickets

Sales end on APR 04

General Admission

Free
2018-04-04 10:00:00 2018-04-04 11:00:00 Discussion on Raw Material Methods and Specifications

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

Fremont, CA, USA Compliance4All DBA NetZealous support@compliance4All.com
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