Syed Imtiaz Haider Livres

The book offers over 20 practical template protocols designed for cleaning validation of commonly used equipment in pharmaceutical manufacturing. Leveraging the authors' extensive experience, it provides technical solutions that address the training needs of professionals in the industry. The focus is on hands-on training and contemporary methodologies, making it a valuable resource for ensuring compliance and improving operational efficiency in finished pharmaceutical production.

This book provides stepwise guidance on how to evaluate, audit, qualify and approve an active pharmaceutical ingredient (API) and packaging material manufacturer and supplier to enhance the GMP within the industry. The book will also be beneficial for institutions conducting pharmaceutical technology courses in terms of GMP and GLP applications.