mdi offers a wide range of validated microfiltration devices such as Capsule and Cartridge filters for sterile filtration of small volume parenteral as well as for sterile venting and air gas filtration. mdi Sterilizing grade product filters are well characterized for its extractables as per BPOG guidelines and exhibit very low extractables and minimum unknows. Every sterilizing grade filters manufactured at in mdi are integrity tested before releasing the batch to market, this ensuring a high degree of reliability Quality Assurance.

mdi as vertically integrated manufacturer of Filtration devices, Tubing and Single Use Systems offers a unique advantage to the producers of SVP, from selection of appropriate sterilizing grade filters & tubing to the design and development of PUPSIT (Pre Use Post Sterilization Integrity Test) & SURF ( Single Use Redundant filtration) assemblies, ready to use Filling line assemblies, also for isolators and RABS systems, integrated with well characterized components which ensure safe flow path for the drug products. mdi offers innovative and customizable solutions to process SVP to meet specific requirement.

asertain^® validation services offer compliance with the global regulatory requirements like Filter Validation, Toxicological assessment, and Leachable Studies for the entire flow path of SUS.

We care for Sterility, Safety, Quality, Purity and Efficacy of your drug product.

Contact us to know more, how mdi can expedite the journey of your Small Volume Parenteral from R&D to the Market.