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U.S.A.

DPS, with its highly specialised biopharmaceutical design capability combined with EPCMV, brings significant project execution capability within the US.

DPS offers an experienced team of multi-discipline professionals with the critical disciplines needed to meet current good manufacturing practices in the design of biopharmaceutical and pharmaceutical facilities. 

Our engineers and architects are specialists in the design of clinical and licensed manufacturing. Our regulatory consultants provide assistance with early planning and cost-effective execution of the validation program.

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