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Dietary Supplements CGMPS - 21 CFR 111 Compliance
This Webinar is over| Date | Jul 23, 2019 |
| Time | 12:00 PM EDT |
| Cost | $150.00 |
|
Online
|
Overview:
Attend this 90 minutes presentation to gain a fundamental understanding of FDA's regulation of Dietary Supplements, Dietary supplements are regulated products, also Dietary supplement marketing, manufacturing, labeling, and advertising are all covered by regulations enforced by FDA.
Why should you Attend:
There is confusion in the industry as just what type of manufacturing controls and record keeping, and labeling content is required by the FDA, and this confusion continues to cause regulatory problems for many new and established companies in this industry.
Areas Covered in the Session:
Required steps for CGMP compliance
Problem areas, common pitfalls
Implementation: Systems, templates and tools
Who Will Benefit:
Engineering
Marketing
Consultants
Interested Consumer Groups
Speaker Profile:
John E. Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/validations, which have passed FDA audit or submission scrutiny, and described in peer-reviewed technical articles, and workshops, world wide.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14@gmail.com
Attend this 90 minutes presentation to gain a fundamental understanding of FDA's regulation of Dietary Supplements, Dietary supplements are regulated products, also Dietary supplement marketing, manufacturing, labeling, and advertising are all covered by regulations enforced by FDA.
Why should you Attend:
There is confusion in the industry as just what type of manufacturing controls and record keeping, and labeling content is required by the FDA, and this confusion continues to cause regulatory problems for many new and established companies in this industry.
Areas Covered in the Session:
Required steps for CGMP compliance
Problem areas, common pitfalls
Implementation: Systems, templates and tools
Who Will Benefit:
Engineering
Marketing
Consultants
Interested Consumer Groups
Speaker Profile:
John E. Lincoln is a medical device and regulatory affairs consultant. He has helped companies to implement or modify their GMP systems and procedures, product risk management, U.S. FDA responses. In addition, he has successfully designed, written and run all types of process, equipment and software qualifications/validations, which have passed FDA audit or submission scrutiny, and described in peer-reviewed technical articles, and workshops, world wide.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14@gmail.com
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