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Dietary Supplement Virtual GMP Refresher

Presented by EAS Independent Consultant Presented by Tamika Cathey

January 18-19, 2022 from 11am-3pm eastern

The Good Manufacturing Practices (GMP) dictated in FDA’s 21 CFR 111 require that “Each person engaged in manufacturing, packaging, labeling, or holding, or in performing any quality control operations, must have the education, training, or experience to perform the person’s assigned functions”. In order to maintain compliance with this requirement, most companies require that employees attend an annual GMP refresher training. Training programs ensure a deeper understanding of how to perform specific job responsibilities in a GMP-compliant manner.

Our 8-hour GMP Refresher training will detail an overview of expectations and compliance requirements to help employees stay on top of critical issues pertaining to GMPs. This training is designed to simplify your annual GMP refresher training requirements in a personalized setting and provide an opportunity to learn directly from our GMP expert. It is not, however, designed for those new to the Dietary Supplement GMP regulations.

Who Should Attend?

Individuals involved in the manufacturing, labeling, packaging, storing and distribution of dietary supplements. In addition, members of the management, regulatory affairs, and quality control/assurance teams would benefit from this training.

About the Instructor

Tamika Cathey

Tamika Cathey consults with an international client base on regulations pertaining to safety and quality of pharmaceuticals and dietary supplements. She evaluates client compliance readiness by conducting audits, risk assessments and mock FDA/GMP investigations and works to design improvement programs based on findings. Tamika has a B.S. in Biology from Greensboro College in North Carolina. Prior to consulting she held positions such as Associate Director, Regulatory Affairs for Charles River Laboratories, and Consumer Safety Officer at FDA’s Atlanta District. She is a certified auditor with the Natural Products Association and holds FDA Level II certifications for the Clinical Bioresearch Monitoring Auditor and Drug Auditor Program

Registration

$199 for EAS, Certified Group and FSNS clients
$249 general registration

* discounts may apply

$199.00$249.00

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Discounts

Two or more registrants from same company – 10% (use GROUP10 discount code at checkout)

Federal or state employees – 50% discount (use GOV50 discount code at checkout)

* only one discount code may be used

Cancellations

Cancellations will be refunded minus a $25 processing fee up to two weeks prior to the start date of the seminar. After this date, no refunds will be given.

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Posted in Dietary Supplements, Seminar.