Speech-generating device

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.

Global Speech Generating Devices Market Trajectory & Analytics: A US$423.8 Million Market by 2027, Growing at a CAGR of 10.8% over the period 2020-2027 - ResearchAndMarkets.com

Retrieved on: 
Monday, August 23, 2021
Technology, Consumer Electronics, VoIP, CAGR, Picture communication symbols, Growth, Speech-generating device, Text, Speech, Pet, Video game

The "Speech Generating Devices - Global Market Trajectory & Analytics" report has been added to ResearchAndMarkets.com's offering.

Key Points: 
  • The "Speech Generating Devices - Global Market Trajectory & Analytics" report has been added to ResearchAndMarkets.com's offering.
  • The global market for Speech Generating Devices estimated at US$206.2 Million in the year 2020, is projected to reach a revised size of US$423.8 Million by 2027, growing at a CAGR of 10.8% over the analysis period 2020-2027.
  • Synthesized Speech Devices, one of the segments analyzed in the report, is projected to record a 10.5% CAGR and reach US$187 Million by the end of the analysis period.
  • The Speech Generating Devices market in the U.S. is estimated at US$55.7 Million in the year 2020.

Eye Tracking for AAC as Accessible as Oxygen: Cognixion® Expands Access to Its Eye Tracking Technology Through Nationwide Oxygen Supplier

Retrieved on: 
Tuesday, June 9, 2020
Venture capital, Audio, Video, Optical, Hardware, Health, Consumer electronics, Professional services, Technology, Speech and language pathology, Occupational therapy, Speech-generating device, Articles, Language, Academic disciplines

Santa Barbara, California-based neurotech company, Cognixion, announced the release of the Expression Eye speech generating device in conjunction with Lincare AAC.

Key Points: 
  • Santa Barbara, California-based neurotech company, Cognixion, announced the release of the Expression Eye speech generating device in conjunction with Lincare AAC.
  • View the full release here: https://www.businesswire.com/news/home/20200609005279/en/
    Expression Eye Series speech-generating device with Facial and Eye Tracking AAC powered by Speakprose.
  • (Photo: Business Wire)
    The Speakprose Pro+ app allows people to quickly access expressive communication via hands-free eye-tracking and facial recognition interface controls.
  • Cognixion and Lincare AAC are making their solution available nationwide.