SteriPack Poland GMP facility granted Pharmaceutical manufacturing authorization for Medicinal Products

On 17 February 2014, SteriPack Poland has been granted Pharmaceutical manufacturing  authorization for Medicinal Products. After extensive inspection and qualification by the Main Pharmaceutical Inspectorate in Poland, the Certificate GIF –IW-N-4000/WTC432/14/13 allows Permission for SteriPack Poland to pack medicinal products.

Marta Karwan Sales & Marketing Director SteriPack Poland says the new strategic development into the pharma industry signals the company’s commitment to broadening our contract manufacturing services portfolio. This is an excellent opportunity for us, says Karwan, to transfer years of experience in medical devices into a new regulatory environment and offer our services to the pharmaceutical industry.

With our unique combination of expertise and capabilities to offer drug-device products we count on facilitating the growth of our Customer’s business as well as SteriPack.

The new operation phase provides maximum flexibility and continuity in the manufacturing processes working in state-of-the-art classified facilities  including a new Cleanroom Class D and Packaging Area with controlled temperatures as well as  Pharmaceutical Warehousing.

SteriPack operates towards the highest standards of ISO 13485  and GMP to handle medical devices and medicinal products. The staff consisting of 190 employees have profound expertise in the production, assembly and quality control of Medical Device and Pharmaceutical Products.

Share Button