WEBINAR: FDA’s LDT RULE: Steps to Prepare for Your FDA First Milestone Submission
$69.95 – $199.00
Individual registration: $79.95
Early Bird Pricing: $69.95 if registered by November 1
Corporate Site License – 12 individual logins for your team members: $249.00
Early Bird Pricing: $199.00 if registered by November 1
No single regulatory development will have greater impact on your lab’s clinical service menu and financial performance than the urgent need to comply with the FDA’s LDT rule. With the compliance clock ticking and the first regulatory milestone arriving in May 2025—just eight months from now—you now have the opportunity to learn the most productive steps necessary to protect the LDTs essential to patient care and your lab’s finances!
This second LDT webinar in our well-attended, ongoing series delivers to you and your team a clear path forward for achieving the twin goals of preserving your LDTs with the greatest clinical value while safeguarding the indispensable revenue generated by those same LDT. You will have the opportunity to ask questions and interact with each of the three knowledgeable experts during the webinar event. You’ll get answers tailored to your lab’s unique situations.
Additional information
| Product Type | Individual Registration, Corporate Site License |
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