In pharmaceutical manufacturing, cleaning validation is an essential stage of verifying that the manufacturing process is suitable. As an integral stage of the cleaning validation program, analytical ...

DSI can supervise the development of analytical methodologies for use in the control of starting materials, drug substances, and drug products. Image Credit: DS InPharmatics This covers the complete ...

Course Topics Include: – FDA, ICH and USP Validation Requirements – Applying Validation Studies Consistent with Method Purpose – GMP Compliance during Validation – Validation Acceptance Criteria – ...

A randomized, multicenter clinical trial to determine the efficacy and safety of pegfilgrastim (GEMA BIOTECH) compared to pegfilgrastim (Roche) for prevention of chemotherapy induced neutropenia in ...

WEST LAFAYETTE, Ind. — A patent-pending innovation created and validated in Purdue University’s College of Engineering could strengthen pharmaceutical research and development in the areas of batch ...

Mankind Pharma collaborates with Denovo Sciences for AI-driven drug discovery, aiming to enhance candidate quality and reduce ...

Bioprocessing technology industrial applications now extend well beyond the pharmaceutical sector. The bioreactor, the membrane filter, and the process analytical technology sensor were built for ...