Dietary Supplements and Nutraceuticals: Compliance with FDA's Current Manufacturing Requirements
June 5, 2013 - Palo Alto CA US

Phone: 650-620-3915
Fax: 650-963-2556

Areas Covered in the Seminar: Key manufacturing issues related to dietary supplements and nutraceuticals. Raw material sourcing, validation, accountability, and documentation techniques. Facility design and planning issues. SOP and training requirements. How do these changes impact products currently in the market. Techniques to ensure compliance at international manufacturing sites. Learning Objectives: Learn how to be compliant with current GMP requirements in the US for dietary supplements in less than an hour to increase credibility of existing products and make it easier to launch more products in the US market in the near future. Who Will Benefit: This webinar will provide valuable assistance to all personnel in: Manufacturers and marketers of dietary supplements QA/QC/Compliance/Regulatory affairs professionals Regulatory and quality professionals working in companies involved in manufacture and sale of dietary supplement, nutraceuticals and similar products Regulatory and quality professionals working for US companies that are considering the purchase of such products manufactured in non-US markets or vice versa Regulatory, compliance and quality professionals consulting with companies developing such products for the US market Business professionals looking to understand the risks and benefits of investing in such products Senior management of such companies in India, China, Africa and Latin America considering marketing their dietary, nutraceutical and similar products in the US

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