Dietary Supplements
July 1, 2009
Dear Valued Dietary Supplement Customer,
Effective June 29, 2009, I have joined the premier regulatory compliance organization of Lachman Consultant Services, Inc. as a Senior Associate. Headquartered in Westbury, New York, Lachman has been dedicated to providing expert regulatory, compliance and science and technology services to the dietary supplement, pharmaceutical, medical device and biotechnology industries since 1978.
In addition to my expertise, you now have at your disposal over 150 Lachman Associates located throughout the United States who are fully knowledgeable with all aspects of the development, regulatory filing, quality and manufacturing processes, inspectional activities and post marketing surveillance requirements. This comprehensive staff is comprised of former industry senior executives, as well as senior level FDA officials, senior scientists and manufacturing and technical experts whose wealth of experience includes such areas as Laboratory Operations, Product Development, Engineering, Facilities, Equipment, Manufactuing and dealing with FDA.
Please note that the following regulatory compliance aides that have been provided through Quality Systems Design, Inc. are still available for purchase:
- Code of Federal Regulations (21 CFR Part 111) PocketGuide
- Your Sourcebook for Dietary Supplement Compliance
(authored by Michael J. Plover)
- Dietary Supplement Standard Operating Procedure Templates
You may also contact Dr. Sturgeon to explore strategies that Lachman can offer for helping you set, reach or maintain your compliance initiatives.
As FDA has actively begun enforcement of the GMPs at medium-sized dietary supplement companies, the time to assure you are in compliance is NOW.
Michael J. Plover
Senior Associate
Lachman Consultant Services, Inc.