Pharmaceutical
Reference Materials for Pharmaceutical Testing
Our comprehensive experience in creating quality pharmaceutical analytical reference materials will help you comply with guidelines set by the United States Pharmacopeia and the International Conference on Harmonization to provide accurate, quantifiable results for the metal analysis of drugs, pharmaceutical substances, and raw materials. You get numerous advantages with our pharmaceutical reference materials:
- Certified for multiple analytical methods (e.g., EU. Ph, JP, USP, ICH, FDA, AOAC, etc.)
- COA includes purity and certified values for a variety of analytical techniques
- Accurate and robust chemical and microbiological-certified reference materials
- Custom reference material manufacturing capabilities under ISO 17034. Learn More
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Complete line of compendial strains for USP 51 and USP 61/62
Qualitative Reference Cultures for USP 51 and USP 61/62
Manufactured from USP specified pure organism strains using media and procedures conforming to USP specifications. These CRMs are manufactured no more than 2 passages from the primary culture.