Featured Product In Submissions and Approvals
Using Real-World Evidence in Drug and Device Submissions
$397.00
Acquire insights into the ideal RWE/RWD data to use in your product applications today with Using Real-World Evidence in Drug and Device Submissions. Read More
Submissions and Approvals
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
$129.00
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