Medical Devices- Regulatory Pathway's
Regulatory Pathway's What you will learn Can provide a precise diagnosis which might affect the medical management of symptoms, or provide treatment options. We are…
ISO 13485 Demystified – Medical Devices’ QMS 360° Insights
Basic understanding on ISO 13485:2016 International Standard on Design and Development Process in Medical Devices What you will learn Students who want to learn the…
IEC 62304 – Medical Devices Software Development & Processes
Software development and maintenance lifecycle with the perspective of risk management as per IEC 62304 and FDA What you will learn Comprehend the IEC 62304…
ISO 13485: Medical Devices QMS Certification Masterclass
Learn ISO 13485 from scratch for medical devices development, production, storage and distribution or installation What you'll learn Learn all ISO 13485 characteristics including the…
ISO 14971 – Medical Devices Risk Management Assessment
ISO 14971 Lead Practice Exam - Course to assess yourself on ISO 14971 knowledge on Medical Devices Risk Management What you will learn Sample Practice…
21 CFR Part 820 (Medical Device QSR) – Practice Exam
21 CFR Part 820 Exam - Self Assessment Exam to validate your QSR knowledge, Medical Devices Regulatory Framework etc. What you will learn Sample Practice…
ISO 13485:2016 QMS – Lead Auditor Preparation Exam
ISO 13485 Practice Exam | Validate QMS Standard knowledge, Medical Devices Regulatory Framework | Audit Case Studies What you will learn Sample Practice exam for…
Medical Device Regulations
Learn about the medical device industry and how to bring new products to market 510K, PMA, De Novo, ISO13485 and beyond! What you will learn…
First do no harm; Baroness Cumberledge Report 2020 Continued
Primodos What you will learn Students will continue their learning of the 'First do no harm' report, that was produced by Baroness Cumberledge and her…