_software-validation-documentation-for-medical-devices-fda-estar-preview-1.jpg "Software Validation Documentation for Medical Devices - FDA eSTAR from fda medical device standards Video Screenshot Preview 1")
Gallery_software-validation-documentation-for-medical-devices-fda-estar-preview-3.jpg "Software Validation Documentation for Medical Devices - FDA eSTAR from fda medical device standards Video Screenshot Preview 3")
Gallery_software-validation-documentation-for-medical-devices-fda-estar-preview-hqdefault.jpg "Software Validation Documentation for Medical Devices - FDA eSTAR from fda medical device standards Video Screenshot Preview hqdefault")
GalleryPlay Video:
(Note: The default playback of the video is HD VERSION. If your browser is buffering the video slowly, please play the REGULAR MP4 VERSION or Open The Video below for better experience. Thank you!)
Jump To Video Parts
⏲ Duration: 54 minutes 27 seconds
👁 View: 390 times
Play Audio:👁 View: 390 times
Description:
Medical Device Academy
Medical Device Academy
Share with your friends:
Whatsapp | Viber | Telegram | Line | SMS
Email | Twitter | Reddit | Tumblr | Pinterest
Related Videos
_understanding-the-difference-between-fda-approval-and-fda-clearance.webp "MedTech Crossroads")
_whats-new-in-fda-estar-v5-0.webp "Medical Device Academy")
_a-conversation-with-robert-hankin.webp "Robert A. Hankin, Ph.D. has served as President and CEO of the Health Industry Business Communications Council (HIBCC) since 1987. In that capacity he has overseen the development of HIBCC from its’ early formation as a bar code labeling standards group to its’ current status as a provider of internationally-accredited healthcare supply chain product and customer identification standards. HIBCC has been designated as a Unique Device Identifier (UDI) Issuing Agency for the US Food and Drug Ad")
_fda-requirements-for-device-labeling.webp "GlobalCompliance Panel")
_medical-device-regulations.webp "On Tuesday, July 15, 2014 at 2:00 p.m. (ET), The TASA Group in conjunction with medical device expert Christina Bernstein presented a free, one-hour, interactive webinar, Medical Device Regulations, for all legal professionals.nnMs. Bernstein discussed FDA medical device regulations.She covered the code of Federal Regulations, as well as the classes of medical devices and special cases for IDE and pediatrics.Ms. Bernstein also provided information on FDA product code databases, FDA inspectio")
_regulatory-standards-amp-risk-management-in-medical-devices.webp "BMESociety")
_compliance-with-medical-standards-iec-62304-iso-14971-iec-60601-fda-title-21-cfr-part-11.webp "Codebeamer, a PTC technology")
⏲ 48 minutes 2 seconds 👁 1.9K
_margaux-boyaval-pmp-and-ryan-shafer-idsa-124-from-hospital-to-home-considering-color-in-medical-devices-and-consumer-hea.webp "2013 IDSA Northeast District Design ConferencenHartford, CTn04.20.13nnAbout the Talk: Color is a critical consideration in the usability and user experience of any health-care product. As more medical devices are adapted for home use, identifying and using color effectively becomes a delicate balance. In this session, Ximedica’s human factors industrial design team draws from its research in health-care settings to provide provocative insights in how to use color in accordance with FDA and AAM")
⏲ 5 min 64 sec ✓ 26-Jun-2014
_understanding-the-difference-between-fda-approval-and-fda-clearance.jpg)
_whats-new-in-fda-estar-v5-0.jpg)
_a-conversation-with-robert-hankin.jpg)
_fda-requirements-for-device-labeling.jpg)
_medical-device-regulations.jpg)
_regulatory-standards-amp-risk-management-in-medical-devices.jpg)
_compliance-with-medical-standards-iec-62304-iso-14971-iec-60601-fda-title-21-cfr-part-11.jpg)
_margaux-boyaval-pmp-and-ryan-shafer-idsa-124-from-hospital-to-home-considering-color-in-medical-devices-and-consumer-hea.jpg)
![[+]](/images/menu.gif){kind=small}