SteriPack Poland Receives Pharma Manufacturing Authorisation 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 SteriPack Poland to pack medicinal products.

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

The new operation provides maximum flexibility and continuity in its manufacturing processes with 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 to the highest standards of ISO 13485 and GMP to handle medical devices and medicinal products. The staff consists of 190 employees possessing extensive expertise in the production, assembly and quality control of medical device and pharmaceutical products.

SteriPack Poland, +48 71381 8199, www.steripackgroup.com.