UK Notified Bodies

An Introduction to the Medical Device Regulation Training Course: In-Depth Insight Into the European MDR Legislation - ResearchAndMarkets.com

Retrieved on: 
Wednesday, April 19, 2023
Medical Devices, Health, CE, Medicine, BSI, Medical device, QMS, Classification, Marketing, ISO, Pharmaceuticals and Medical Devices Agency, Writing, European Medicines Agency, UK Notified Bodies, Medication, Notified body, Technical director, Research, European Medical Devices Industry Group, Bachelor of Science, NextGen Healthcare, EMA, MHRA, European, Certification, ISO 13485, Pharmacy, R, Competent authority, Speech-generating device, Test management, Clinical, LRQA, Pharmacist, Nursing, Management

She has extensive experience of conducting clinical studies with medical device products as well as regulatory expertise for CE marking of devices.

Key Points: 
  • She has extensive experience of conducting clinical studies with medical device products as well as regulatory expertise for CE marking of devices.
  • Specifically she has been involved in writing and reviewing hundreds of Clinical evaluation reports for the medical device industry, she ahs also provided training to Notified bodies in this subject.
  • Janette sits on several committees in the device community and industry and has been an instrumental advocate of improving and advancing medical device research in the UK.
  • Her first introduction to the Medical device Industry was as the R&D Manager for a medical device manufacturer, with responsibility for the development of several device drug combination products, with the core technology utilizing bovine collagen.

An Introduction to the Medical Device Regulation Training Course: London, United Kingdom - August 1-3, 2022

Retrieved on: 
Friday, July 29, 2022
ISO, Medication, R, Pharmacist, Pharmaceuticals and Medical Devices Agency, Clinical, MHRA, Industry, Medicine, European Medical Devices Industry Group, Notified body, European, ISO 13485, Bachelor of Science, Research, NextGen Healthcare, EMA, Non-functional testing, Marketing, Classification, Pharmacy, CE, Solution, UK Notified Bodies, Speech-generating device, QMS, European Medicines Agency, BSI, LRQA, Medical device, Competent authority, Department, Technical director, Certification, Writing, Management

She has extensive experience of conducting clinical studies with medical device products as well as regulatory expertise for CE marking of devices.

Key Points: 
  • She has extensive experience of conducting clinical studies with medical device products as well as regulatory expertise for CE marking of devices.
  • Specifically she has been involved in writing and reviewing hundreds of Clinical evaluation reports for the medical device industry, she ahs also provided training to Notified bodies in this subject.
  • Janette sits on several committees in the device community and industry and has been an instrumental advocate of improving and advancing medical device research in the UK.
  • Her first introduction to the Medical device Industry was as the R&D Manager for a medical device manufacturer, with responsibility for the development of several device drug combination products, with the core technology utilizing bovine collagen.

An Introduction to the Medical Device Regulation Training Course: London, United Kingdom - August 1-3, 2022 - ResearchAndMarkets.com

Retrieved on: 
Tuesday, July 26, 2022
Medical Devices, Health, ISO, Medication, R, Pharmacist, Pharmaceuticals and Medical Devices Agency, Clinical, MHRA, Industry, Medicine, European Medical Devices Industry Group, Notified body, European, ISO 13485, Bachelor of Science, Research, NextGen Healthcare, EMA, Non-functional testing, Marketing, Classification, Pharmacy, CE, Solution, UK Notified Bodies, Speech-generating device, QMS, European Medicines Agency, BSI, LRQA, Medical device, Competent authority, Department, Technical director, Certification, Writing, Management

She has extensive experience of conducting clinical studies with medical device products as well as regulatory expertise for CE marking of devices.

Key Points: 
  • She has extensive experience of conducting clinical studies with medical device products as well as regulatory expertise for CE marking of devices.
  • Specifically she has been involved in writing and reviewing hundreds of Clinical evaluation reports for the medical device industry, she ahs also provided training to Notified bodies in this subject.
  • Janette sits on several committees in the device community and industry and has been an instrumental advocate of improving and advancing medical device research in the UK.
  • Her first introduction to the Medical device Industry was as the R&D Manager for a medical device manufacturer, with responsibility for the development of several device drug combination products, with the core technology utilizing bovine collagen.