Announcing the 2025 Outsource! Week
Register today to access these curated webinars live or on demand.
Advertisement
Register today to access these curated webinars live or on demand.
Advertisement
As regulatory bodies like the FDA and USP continue to emphasize method validation and bioequivalence, laboratories must ensure their dissolution testing practices are scientifically sound and regulatory compliant.
Rigorous analytical testing ensures that APIs meet the highest standards for identity, purity, potency, and stability—safeguarding patient health and maintaining market confidence.
Tentamus' network of highly specialized laboratories aim to offer on-site safety and quality testing services in the shortest time possible
This CDMO specializes in new chemical entity (NCE) molecule, NDA 505(b)(2), and ANDA development programs
This CRO has a fully-equipped analytical laboratory and a lab-scale packaging facility
This CRO delivers FDA ready, cGMP-compliant analytical solutions quickly to keep drug development programs on track
Since 1998, this contract laboratory provides analytical and microbiological testing for the pharma industry.
They develop and perform GMP potency assays for a wide variety of drugs, proteins, monoclonal antibodies, vaccines and gene therapies
By understanding the advantages and limitations of each approach, pharmaceutical manufacturers and quality control laboratories can design robust, efficient microbial testing programs.
As sea moss becomes increasingly popular, ensuring its safety and efficacy is critical.
Advertisement
Advertisement