- Introduction to Medical Device and regulations – Webinar Course
- Clinical evaluation of medical devices for regulatory compliance – Webinar Course
- Live Webinar Regulation 2017/745 on Medical Devices: technical file structure – Webinar Course
- Live Webinar Regulation 2017/745 on Medical Devices: post market activities and follow up – Webinar Course
- Regulation 2017/745 on Medical Devices: Unique Device Identification – Webinar Course
- Biological Safety Evaluation Live Webinar: Drafting of the Biocompatibility report in accordance with ISO 10993-1- Risk Approach – In Vivo – In Vitro Test – Technical File – Webinar Course
DESIGN & QUALITY CONTROL
- Design Control 21 CFR 820.30 – Webinar Course
- New ISO 13485:2016 Medical Device QMS Transition Training – Recorded Webinar – Webinar Course
- Medical Device Sterilization Process: ETO, GAMMA, STEAM, SHELF Life, Validation – Webinar Course
- New – Clean Room Live Webinar: New ISO 14644:2015, design and construction, proof of continuous compliance, personnel behaviour – Webinar Course
FDA AND US DIRECTIVE
- DESIGN CONTROL 21 CFR 820.30 – Webinar Course
- FDA REGISTRATION: MEDICAL DEVICES, IVD, COMBINATION PRODUCTS – Webinar Course
- How FDA Trains Its Investigators to Review CAPA, and Best Practices for Preparation – Webinar Course
R&D AND TECHNICAL
NEW ! Bioabsorbable material for Implantable Medical Device – Webinar Course
Free – INJECTION MOLDING PROCESS OVERVIEW – Webinar Course