Medical Devices and Regulatory Affairs
Self Learning Course What you will learn Learning a Medical Devices and Regulatory Affairs course can provide you with the necessary skills and knowledge to…
Medical Devices and Regulatory Affairs
Self Learning Course What you will learn Learning a Medical Devices and Regulatory Affairs course can provide you with the necessary skills and knowledge to…
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…