Key Standards Supporting Good Distribution Practices
The key standards to help pharmaceutical organizations implement Good Distribution Practices are as follows:
BS EN ISO 9001 Quality management systems help companies identify gaps in their good manufacturing practices, proactively mitigating risk before problems arise. Benefits of this standard include; helps to assess gaps in quality management systems to identify areas of higher risk, develop and implement plans to remediate quality risks, and assist in developing quality management systems to bolster compliance.
BS ISO 28000 Risk management in supply chains enables organizations to understand hidden risks in their supply chain and equips them to handle unforeseen disruptions. This standard helps organizations to map risk across the supply chain, from API manufacturers to distributors and sites of care, develop and implement plans to respond to, and remediate supply chain risks (including manufacturing, in-transit, and distribution-related risks) and develop business impact analysis and business continuity plans.
BS EN ISO 22301 Business continuity management standards help pharmaceutical organizations understand and prioritize the threats to their business with the international standard for business continuity. It specifies the requirements for a management system to protect against, reduce the likelihood of, and ensure your business recovers from disruptive incidents.
Ensure your pharmaceutical organization is working to good distribution practices, by adding these standards to your collection today.