Botanical and Supplement Testing
Need a laboratory that can assist with the revised cGMP regulations? Eurofins Nutraceutical Center offers core analytical capabilities for botanical, herbal, natural products, and dietary supplements such as:
- Heavy Metals Testing of Botanicals and Supplements by ICP and ICP-MS
- Pesticides Residue Testing of Botanicals, FDA, AOAC (Quechers), European, or USP methods
- Private Laboratory Submission of Analytical Data for FDA Import Detentions
- Risk Assessment of Contaminants in Imported Botanical Products
- Residual Solvent Testing by USP methods
- cGMP Consulting
At the Eurofins Nutraceutical Center in Petaluma, CA, complete dietary supplement capabilities include:
- Product Quality Control and Release Testing
- Raw Material ID and Purity Assay
- Pre-clinical Study Support
- Noncompendial Method Development
- Stability Testing
- Determination of Impurity Profiles in Nutraceutical Products
- Identification of Unknowns and Characterizations of Mixtures
Scientific Achievements of Eurofins US Laboratories
- Application of Capillary Electrophoresis Methods for Demanding Analyses Involving the Separation of Small Organic Molecules in Complex Matrices
- First to Develop Analytical Methods for Creatine & Impurities, Caffeine and Synthetic / Natural Ephedra Isomers Found in Sports Nutrition and Thermogenics Products
- Successful Submission of Data Packages to FDA for Pesticide Residues in Imported Ginseng Extracts
- Successful Transfer of European Pesticide Methods to US Competence Centers
- Application of Headspace GC-MS Methodology to USP Residual Solvent Testing, thereby Increasing Sensitivity and Selectivity of the Analysis
- Application of Modified Quechers Methods to Pesticide Testing of Botanicals
- Participation in Multiple-Laboratory AOAC Method Validation Studies for New Analytical Methods for the Testing of Botanicals and Supplements
For more information, Contact Us.