The API-excipient compatibility analysis provided by CD Formulation can provide effective data for the selection and determination of formulation excipients and formulation technology for drug ...

Propylene glycol (PG) is a clear, odorless, and viscous liquid that is miscible with water and many organic solvents. It is a small molecule that is structurally different and unrelated to PEG, ...

Increasingly stringent audit requirements will make third-party accredited GMP audits critical for pharmaceutical excipients and raw materials. In today’s regulatory environment, and with the ...

The authors present an update to the Wyeth/BASF experience with the IPEC Novel Excipient Safety Evaluation Procedure. Historically, the development of novel excipients has been hampered by the global ...

A vital parameter in pharmaceutical samples is loss on drying, which is utilized to determine the amount of water and other volatile solvents in a sample, as it can impact a product's stability, ...