MediWound announces successful GMP audit by the Israeli Ministry of Health

The IMOH conducted the audit as a part of routine inspection of the Company’s manufacturing facility for its proteolytic enzyme therapeutics. And the audit concluded that MediWound’s manufacturing facility is compliant to the requirements of cGMP for the manufacture of sterile and biological medicinal products. This compliance status is valid for three years from the time of the audit. As the IMOH is also a member of the Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme, this audit is also issued under the provisions of the Conformity Assessment and Acceptance of Industrial Products Agreement between the European Union and Israel.
The Company’s spokesperson said that as a fully integrated company, manufacturing is a core competency of MediWound and is critical for our commercial success. We take great pride in maintaining the highest quality standards and this positive audit underscores the viability, quality and high standards MediWound upholds in the manufacture of our proteolytic enzyme therapeutics for commercial use and for products under development in compliance with rigorous international standards.