Featured Product In Medical Devices
Selecting and Implementing Electronic Document Management Systems in the EU
$197.00
Converting to an electronic document management system (eDMS) is key to increasing your record-keeping efficiency. Only one resource enables you to do that in a cost-effective manner while ensuring compliance with EU regulations: Selecting and Implementing Electronic Document Management Systems in the EU. Read More
Medical Devices
Organizing Data and Document Archives: Finding a Needle in a Haystack for FDA Inspections – Webinar Recording/Transcript
$287.00
Maintaining Your Risk-Based Cleaning and Disinfectant Programs: Best Practices During COVID-19 – Webinar Recording/Transcript
$287.00
Digital Health Regulation: Navigating FDA’s Rules for Software as a Medical Device
$397.00
The MDSAP Audit Process: Latest Developments and Best Practices – Webinar Recording/Transcript
$287.00
Consumer Diagnostics and Wellness Testing: Navigating the Medical Device Regulations – Webinar Recording/Transcript
$287.00
Medical Device Cybersecurity: Understand the Latest Developments – Webinar Recording/Transcript
$287.00
CDRH’s Proposed Rule Harmonizing QSR and ISO 13485: Everything Devicemakers Must Know and Do to Prepare – Webinar Recording/Transcript
$287.00
Medical Device Regulatory Policy: Breakthrough Technologies, STeP and — Wait for It — Reimbursement – Webinar Recording/Transcript
$287.00
Spreadsheet Validation: Best Practices to Maintain Compliance – Webinar Recording/Transcript
$287.00
