GMP complete services for dietary supplements manufacturers

Expectations from consumers regarding safety and authenticity of dietary supplements are increasingly stringent and require manufacturers, all over the world, to stay up-to-date with current regulations and industry practices. Market regulations may vary from country to country but more and more retailers request that their suppliers meet cGMP requirement.

Dietary supplements are a way for consumers to complement their diet in order to improve their health, manage their weight, enhance sport as well as sexual performance, etc. They are taken orally and contain a “dietary ingredient” such as vitamins, minerals, amino acids, bee products (royal jelly, propolis, bee brad, etc.) and herbs or botanicals, as well as other substances that can be used to supplement the diet. It is important to note that dietary supplements are not medicinal products and may not contain articles that are approved as new drugs, other undeclared drug ingredients, or make disease claims.
Whether they are marketed in the United States or in a EU Member State, dietary supplement products have to comply with all relevant aspects of FDA or EU food legislation and any specific EU Member State national legislation in terms of their composition, manufacture and control.

cGMP audit for dietary supplement manufacturers

Dietary supplement manufacturers will benefit from our global network of food & healthcare experts to get audited against recognised standards based on cGMP and gain retailers’ trust and consumer confidence.
Eurofins Food & Healthcare Assurance teams are offering the following audit programmes and are available to help you choose the best solution for your specific need.

Audits we offer:

• Eurofins’ proprietary GMP 21CFR111
• SSCI certification
• GRMA certification
• GMP IADSA
• GMP FSE
• GMP EHPM

Access additional services for dietary supplements through our unique one-stop shop.