Qualified reference standards are indispensable for method validation, screening and pharmacokinetic studies. Precisely monitored parameters must be used in the storage of reference standards. Sampling, packing and shipping must meet the pharmaceutical guidelines.
We supply qualified reference standards with a Certificate of Analysis (CoA). This is also available for substances not available commercially or for special requests (e.g. by- and degradation products). This CoA contains information including the durability, transport and storage conditions of the reference standard. All reference standards are analyzed and qualified using the most state-of-the-art technology in our GMP certified laboratories.
A summary of reference Standards:
- Synthesis of reference standards, including complete characterization
- Preparative isolation of reference standards and complete characterization
- Storage, packaging and shipping of reference Standards
- Delivery of a GMP – CoA for reference standards