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We are one of the few companies that can support our partners with such items as: 
• Certificate of Good Manufacturing Practice (GMP). 
• Certificate of Analysis (COA) with every batch. 
• Stability report of finished product. 
• Independent product testing & tech data to assure product quality. 

We hope to share our belief and vision with like-mind organizations. If you are interested in becoming an agent or distributor 
please complete the form below. Response time is 2-3 business days, depending on the nature of the question. 

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Swissmed offers in-licensing development of generic pharmaceuticals in our R&D Center as well as outsourcing of full size commercial batch production. In addition our regulatory affairs team is able to compile technical data as per country specific dossiers and may assist in carrying out bioequivalence studies through relevant clinical research organizations as per required guidelines. Further, we have the capability of manufacturing final dosage forms in country specific GMP approved facilities.