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CBD|GMP|Supplements|Pharmaceuticals

Business + Compliance + Quality=
Simply to Market©

 

About our Company

Our company specializes in helping you navigate the current fluid regulatory landscape of the CBD, GMP, supplements and pharmaceutical compliance arena. We can assist you from field to finished product by developing and implementing good agricultural practices, product development strategies, quality systems, and manufacturing compliance plans. The combination of our business, regulatory and quality management experience are combined to assist you with your journey from inception to marketplace

About Managing Director, Cheryl R. Dicks, MSc., RAC, PCQI

Cheryl brings over 20 years’ of experience in the Regulatory and Quality arenas covering all phases of product development, manufacturing, and quality system(s) implementations for the food, dietary supplement, infant formula, and pharmaceutical industries.

With humble beginnings in the dietary supplement industry as an entrepreneurial business owner investigating the quality of the product sold to her customers, to lobbying for the passage of DSHEA, and serving as a Natural Products Association executive board member, her quality and regulatory experience is based on experience and a foundational Master’s of Science education in Biomedical Sciences, concentrating  in biochemistry and Regulatory Affairs. 

Having achieved the coveted Regulatory Affairs Certification  (RAC), her Master Thesis focused on regulatory development strategies for dietary supplements through the drug approval pathway and cGMP compliance for the industry.

Cheryl’s extensive experience has included key positions in Regulatory, Quality, and Operations in both the military, CRO and private sectors.  Her broad experience extends from work with farmers on good agricultural practices and organic certifications for crops and livestock to a new drug, drug/device and dietary supplement product development strategies, quality, and cGMP manufacturing compliance as well as supporting essential regulatory filings and clinical trials for these arenas.

Her extensive experience in working with regulatory Agencies has aided clients in working for a positive outcome with  U.S. and Canadian regulatory personnel.