Site Standard Operating Procedure for Vendors Approval

Drug companies which are considerably large have large in-house sourcing and procurement teams to perform these functions internally. The active pharmaceutical ingredients (APIs) which are used as starting materials in the production of medicinal products are manufactured under the strict good manufacturing practice regulations so that their quality, safety, and efficacy are ensured and which further ensures that patients worldwide and at any time can have confidence in the quality, safety, and efficacy of medicines. The objectives of all the countries, regions, and companies are nonetheless the same, that is to deliver the medicines which are manufactured under the health regulatory bodies' policies, procedures, and guidelines and which are safe to use, high in quality and efficacy to treat diseases and to prevent adverse events that may result in death or serious illnesses, or product recalls resulting from deficiencies in the manufacturing and distribution processes.