WEBINAR: FDA’s LDT RULE: Understanding What’s Compulsory, What’s Not!
$79.95 – $249.00
Individual registration: $79.95
Corporate Site License – 12 individual logins for your team members: $249.00
You will have the opportunity to ask questions and interact with each of these three knowledgeable experts during the webinar event. You’ll get answers tailored to your lab’s unique situations.
Laboratories face unprecedented challenges with this ruling and may need to make some difficult decisions regarding their LDT menus. Despite ongoing litigation against the new rule, the FDA expects laboratories to implement the full FDA Medical Device Quality System and be in compliance by May 6, 2025—followed by other compliance requirements for 2026 and 2027. It’s one compelling reason why this webinar is a “must attend” for you and key members of your team.
Additional information
| Product Type | Individual Registration, Corporate Site License |
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