Featured Product In Regulatory Affairs
Using Real-World Evidence in Drug and Device Submissions
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Regulatory Affairs
Medical Device Risk Management Tools: FMEA Does Not Equal Risk Assessment – Webinar Recording/Transcript
$287.00
Reliability Assessment for Medical Devices and Combination Products: Meeting FDA Objectives and Requirements – Webinar Recording/Transcript
$287.00
Where Design Control Meets Risk Management: A Lifecycle Approach for Medical Devices – Webinar Recording/Transcript
$287.00
FDA’s New Sterilization Pilot on Risk-Based Cleaning and Disinfectant Programs – Webinar Recording/Transcript
$287.00
The Return of VALID: What the Future Holds for IVDs and LDTs – Webinar Recording/Transcript
$287.00
Real-World Evidence in Drug and Device Submissions: What Regulatory, Compliance & Quality Professionals Need to Know – Webinar Recording/Transcript
$287.00
