Welcome to POLLAND CONSULTING
We advise manufacturers on European and international approval of medical devices of all risk classes according to European and international requirements (e.g. MDD, MDR, FDA, CMDR, UKCA & MDSAP) and quality management systems (e.g. ISO 9001, ISO 13485).
Through our responsible support of manufacturers, Polland-Consulting helps to make medical products safer and minimise risks.
Management Consulting
Support in different areas and quality management according to ISO 9001, ISO 13485, MDSAP and JPAL
Audits
Conducting internal audits and customer audits (1st-party audits), supplier audits (2nd-party audits) and certification audits (3rd-party audits)
Interims Management
Advice in the area of crisis management, bridging staff shortages, controlling, business analysis, cost optimisation
Training
Conducting training courses via the TÜV SÜD Academy for QMF, QMB, QMA, internal auditors and safety officers
Coaching
Technical File Remediation, MDR Implementation and Executive Coaching in Human Resource Management
Corporate philosophy
Above all, the aim is to make a major contribution to making medical products safe and to raise awareness among the manufacturers of these products...