How to become a supplier

Missionpharma only procure products from suppliers that are prequalified by our QA/QC department.

Our prequalification process covers the following steps:

The following outlines the documentation that all suppliers must provide in order to be considered a Missionpharma supplier:

Commercial documentation
 

Quality-related documentation

			Manufacturing licence issued by the National Health Authorities.
			WHO-GMP certificate for all manufacturing sites.
			Duly completed product questionnaire.
			Duly completed manufacturer questionnaire.
			A Site Master File (SMF) for each manufacturing site to be prequalified including a description of the manufacturing site(s).

For more details on additional documents to be provided, go to the Quality Assurance section.

Our QA/QC department thoroughly evaluates the quality-related documentation. If your documentation on products and manufacturing sites is accepted, we arrange for a site inspection to assess compliance with Good Manufacturing Practices (GMP).

The inspection covers all aspects of GMP including premises, equipment, materials, documentation, validation, personnel, production, quality control, water systems as well as production and control-related aspects.

Read more about Missionpharma’s prequalification process.