MedTech Quality and Regulatory Affairs (QARA) Training Open Q&A

Planning ahead on training needs? Looking to budget? Join us on Wednesday, November 6th 2024, from 4pm GMT, where Comply Guru’s Eoin P. Kelly & Michelle Keane will discuss Comply Guru’s MedTech Quality and Regulatory Affairs Training Portfolio. It is an opportunity to hear us talk about our training portfolio, including who should attend, plus get your questions answered.

This Webinar will discuss various training courses including:

• Understanding ISO 13485, ISO 14971 & Other Standards
• Internal and Lead Auditor Training
• EU Medical Device Regulation (MDR 2017/745) and EU In Vitro Diagnostic Regulation (IVDR 2017/746) Training
• FDA QSR vs QMSR for Practitioners and Auditors
• Regulatory Auditing (MDSAP, MDR, IVDR + QMSR)
• Mastering CAPA
• What Other Training We Can Offer
• Q&A

Register for FREE to gain access to this Webinar (Live Event).