The formulation and processing conditions employed in the manufacture of medicinal products can have a significant effect upon their safety, quality and efficacy. Even small changes to the input materials and/or processing conditions can affect attributes such as bioavailability and stability,
which would not typically be detected during routine QC testing. It is very important that as a QP, you understand the principles of formulation and pharmaceutical processing. This module considers the major dosage forms in detail and covers basic formulation principles including preformulation studies, bioavailability considerations and the effect of excipients on physical and chemical stability. It also includes sessions on the Orange Guide Annexes, process validation, scale-up, facility design, utilities and sterilisation processes.
which would not typically be detected during routine QC testing. It is very important that as a QP, you understand the principles of formulation and pharmaceutical processing. This module considers the major dosage forms in detail and covers basic formulation principles including preformulation studies, bioavailability considerations and the effect of excipients on physical and chemical stability. It also includes sessions on the Orange Guide Annexes, process validation, scale-up, facility design, utilities and sterilisation processes.
