Secure your pharma QC.

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Pharmaceutical analysis and quality control (QC) testing compliance with international pharmacopeia specifications are critical from early-stage drug development to release. Trust our analytical chemistry and microbiology testing portfolio, services, and technical solutions to ensure your small molecules, large molecules (biologics or biosimilars) are developed, manufactured, released with the highest degree of safety, purity, and potency as per Good Manufacturing Practice (GMP), and regulatory compliance requirements.

Looking for ADME/DMPK, Drug Product characterization, API Stability, Impurity Profiling, Dissolution Testing, or USP/EP Monograph testing?

We have the fit for purpose products and expertise to help you feel secured about your small molecules, peptides, proteins, monoclonal antibodies (mAbs), antibody drugs conjugates (ADCs), or excipient analysis. Discover our complete portfolio solutions at each stage of your pharmaceutical analysis and QA/QC workflow at the bottom of this page.

Biologics product characterization

Biopharmaceutical drugs and biosimilars are complex to characterize and quantify. Our products, techniques, and experts can support you to ensure a robust and well-specified drug with the highest degree of quality and compliance.

Regulatory compliance & Release Testing

We comply with numerous global standards, such as ISO, ACS, USP, PhEur, and FDA CFRs. We offer compliance guaranteed analytical and microbial testing products and provide regulatory guidance throughout the entire workflow.


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Merck

Research. Development. Production.

We are a leading supplier to the global Life Science industry with solutions and services for research, biotechnology development and production, and pharmaceutical drug therapy development and production.

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