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The PIC/S GMP Guide is divided into two parts and a number of annexes which are applicable to both parts. Part I covers the general GMP principles for the manufacture of finished products. Part II covers GMP for active pharmaceutical ingredients (API) used as starting materials.
Introduction. This guide is intended for those involved in the storage, transportation and distribution of Active Ingredients, Therapeutic Products, Chinese Proprietary Medicines, Cell, Tissue and Gene Therapy Products (CTGTP) and CTGTP starting materials and health products which are used as clinical research materials, collectively referred ...
WHO GDP and GSDP certification can apply to: Wholesalers and other parties, such as brokers, suppliers, distributors, logistics providers, traders, transport companies and forwarding agents of healthcare products with functioning storage and distribution areas, and warehouses.
In December 2023, HSA updated the following Good Distribution Practice (GDP) guides: – GUIDANCE NOTES ON GOOD DISTRIBUTION PRACTICE https://www.hsa.gov.sg/docs/default-source/hprg-ald/guide-mqa-013.pdf.
PHE2018. This module is an introduction to current Good Manufacturing Practice (cGMP) in the pharmaceutical manufacturing environment. This module will cover the background of GMP and the regulatory review for pharmaceutical industries, from drug development to manufacturing of finished products.
Learn Good Distribution Practice (GDP) requirements for regulated industries: handling, storage & distribution of medicines / medical devices. Australia +61 (0)3 9897 1990 Singapore +65 6914 9068
1 paź 2024 · Join our webinar to learn about the World Health Organization's good distribution practice (GDP) and how they help provide a safe and secure supply chain.
