Merck

What if regulatory compliance in Pharma QC came in a pill?

The Top 3 Advantages of the Product
1

We comply with numerous global standards, such as ISO, ACS, USP, PhEur and FDA CFR’s

2

We offer certified analytical and microbial testing products

3

We provide regulatory guidance throughout the entire workflow

We offer an extensive compliant portfolio and provide regulatory guidance

GMP prescription and over-the-counter (OTC) generic drug development, manufacturing and quality control (QC) is one of the most challenging aspects of pharmaceutical work.

We have decades of method development expertise and state of the art QC Analytical and Microbiology testing laboratories that can help. We comply with numerous global and local standards, such as ISO, ACS, USP, PhEur, JP and FDA CFR’s and work with you to ensure the drug development process is safer and more efficient throughout the entire product characterization, method development, manufacturing and quality control process.

We provide comprehensive quality documentation to streamline your accreditation and audits combined with an extensive portfolio of certified analytical and microbial testing products.

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