Why Should You Attend:
In the manufacture of dietary supplements, the FDA, under 21 CFR, Part 111, requires that Master Manufacturing and Batch Production Records be created and maintained. Proper inventory management of raw materials and components has a direct impact on the development and maintenance of master and batch production records.
This webinar explains the proper way to create FDA required Master Manufacturing and Batch Production records. FDA 21CFR Part 111 requires that Master Manufacturing and Batch Production records be created. This webinar will define what each of these requirements is and how to apply them in a production environment to the satisfaction of the FDA. The webinar will also discuss how inventory control techniques have an impact on the process of creating and managing these records.
Areas Covered in the Webinar:
This webinar will cover the following;
Who Will Benefit:
This webinar will benefit those who have production and quality control responsibilities in a Dietary Supplements manufacturing plant.
Chris Stefanadis has over 20 years of Quality Management systems and process improvement experience and is Six Sigma Black Belt certified.
His Quality Management Systems experience includes the development, implementation and management in manufacturing plants and service organizations of ISO 9001, ISO 13485, TS 16949, ISO 14001, GMP, FDA 21 CFR Part 111 and Part 820.
A strong manufacturing background with Nutraceuticals, Medical Devices, Plastic Extrusion & Compression Molding, Acrylic Latex and Chemical Manufacturing has also given him experience with Lean Manufacturing and Process Improvements.
Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).
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