H0312 Herbal Supplements – Legislation

Have a look at our PowerPoint Introduction and Brochure describing deliverables, differentiators and case studies. Eight case studies can also be reviewed.

Objective

The objective of this study was to assist the client in understanding regulatory changes in the market for herbal supplements and the effects of these changes on the herbal supplement market. The client wanted details on the requirements of GAP and GMP legislation and the timescales involved in meeting their standards.

Method

CPL examined current European and US legislation and proposed legislation, and performed interviews with legislators and regulatory bodies. We also interviewed a US herbal manufacturer.

Click here for a PDF of the contents of the study or look below for an outline.

Table of Contents

Objective

Methods

Principal Findings and Conclusions

Contact Reports

    European Agency for the Evaluation of Medicinal Products
    EUREP
    EUROPAM
    Eurpean Union
    Food and Agriculture
    FAO
    Herbal products manufacturer
    Medicines Inspectorate
    U.S. Food and Drug Administration
    WWF

4 Tables

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