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For a product to reach its final users in full compliance with its specifications, assembly and finishing activities must take place in a controlled and well-defined environment. From order intake through final delivery, Medistri follows a structured and validated manufacturing workflow designed to ensure consistency, quality, and regulatory compliance at every stage.

At Medistri, we specialize in the precision-driven assembly, packaging, and sterilization of medical devices or pharmaceutials, catering to both emerging startups and established companies. Our process is designed to support the unique needs of each client, from prototype development to routine large-scale production.

Created for start-up companies and early-stage products, Medistri's manufacturing team can offer primary, sec­ond­ary, and ter­tiary packaging solutions that fit your strategic & regulatory requirements. 

Created for start-up companies and early-stage products, Medistri's manufacturing team can offer primary, sec­ond­ary, and ter­tiary packaging solutions that fit your strategic & regulatory requirements.

Good Manufacturing Practices (GMP) are vital standards in the pharmaceutical industry that ensure product quality and safety throughout production. These regulations protect against contamination, errors, and deterioration, ensuring that healthcare products consistently meet strict standards.

Medistri follows a precise protocol in order to deliver the optimal final outcome within weeks of our collaboration. With Medistri’s GMP authorisation, you can now also introduce pharmaceutical products into your personalised kits.