Push-Med helps to assess the training needs of company personnel and staff.

We provide customized quality and regulatory training, and we develop on-site training programs for company employees on a variety of subjects concerning the design, development, manufacturing, testing, and marketing of medical products, for example:

• Introduction to Regulatory Affairs for medical devices;
• Quality System Principles;
• Quality System inspection and audits;
• Risk Management;
• Post-marketing requirements for medical devices;
• Principles of Good Clinical Practice (GCP);
• Managing and Monitoring of Clinical Trials;
• And more...

We offer unique training development programs based on client needs and personnel characteristics