Description
Good Distribution Practice (GDP) refers to the regulatory guidelines governing the wholesale distribution of medicinal products to ensure their quality and integrity is maintained throughout the supply chain from the manufacturer to the end user. Good Distribution Practice extends beyond the distribution of the finished product and includes the sourcing, storage and transportation and other ingredients prior to manufacturing. Failure to adhere to the guidelines at any point within the supply chain, including all intermediate points of storage and transport, can have a serious impact on the quality of the product. Distributors and Importers require Good Distribution Practice for Medical Devices (GDPMD) certification. Good distribution practice (GDP) deals with the guidelines for the proper distribution of medicinal products for human use. GDP is a quality warranty system, which includes requirements for purchase, receiving, storage and export of drugs intended for human consumption. The GDP requirements consist of 6 parts: 1. Preliminary 2. Organization and GDP Regulatory Compliance System 3. Establishment Responsibilities 4. Resource Management 5. Supply Chain and Device Specific 6. Surveillance and Vigilance