11:00 am: Solve Clinical Trial Enrollment Struggles With Better Utilization of Healthcare Data
11:00 am – 12:00 pm April 5, 2022
Join the Elligo Elite Learning Series round table “Solve Clinical Trial Enrollment Struggles With Better Utilization of Healthcare Data” for expert insights and engaging discussion surrounding the future of EHR data and clinical trial enrollment. This webinar will feature industry leaders from the US Food and Drug Administration (FDA), Freenome, Cerner Enviza, Deep Lens, and Elligo Health Research®.
10:00 am: Webinar: Transitioning from EUA to 510(k) for IVD Products: Planning to Execution
10:00 am – 11:00 am April 21, 2022
Join NAMSA for this webinar where we will dive into the U.S. FDA draft guidance and discuss best practices for identifying gaps and maximizing your on-market product for a successful 510(k) submission
2:00 pm: TMDA Medical Device Funding: Banks, Investors, Grants, etc.
2:00 pm – 3:30 pm April 21, 2022
Panelist discussion regarding various forms of funding within the medical device industry, some obvious and not so obvious. Second half of the event is open to the attendees to ask direct questions to the panelists. We hope you can join us!
All day: The 2022 AMDM Annual IVD Regulatory Meeting and FDA Submissions Workshop Are Going Hybrid
All day April 26, 2022 – April 28, 2022
In an effort to allow attendees to participate and engage in our events no matter where they are, the 2022 Annual IVD Regulatory Meeting and FDA Submissions Workshop, will be held at the Bethesda Marriot Hotel, in Bethesda, MD as a hybrid event allowing for in-person or virtual participation. Mark your calenders. Registration will open by March 1.
All day: The 2022 AMDM Annual IVD Regulatory Meeting and FDA Submissions Workshop Are Going Hybrid
All day April 26, 2022 – April 28, 2022
In an effort to allow attendees to participate and engage in our events no matter where they are, the 2022 Annual IVD Regulatory Meeting and FDA Submissions Workshop, will be held at the Bethesda Marriot Hotel, in Bethesda, MD as a hybrid event allowing for in-person or virtual participation. Mark your calenders. Registration will open by March 1.
All day: Pharmaceutical Testing: Strategies for Elemental Impurities Testing in Pharmaceuticals
12:00 am – 1:00 am April 27, 2022
With regulatory requirements, validation protocol, and data integrity all being in the forefront, it is important to equip the laboratory with more than just analytical equipment. By providing tools, resources and knowledge, PerkinElmer’s total solution approach to USP testing enables laboratories to be analyzing samples faster and ensures compliance with regulations on electronic records and signatures.
All day: The 2022 AMDM Annual IVD Regulatory Meeting and FDA Submissions Workshop Are Going Hybrid
All day April 26, 2022 – April 28, 2022
In an effort to allow attendees to participate and engage in our events no matter where they are, the 2022 Annual IVD Regulatory Meeting and FDA Submissions Workshop, will be held at the Bethesda Marriot Hotel, in Bethesda, MD as a hybrid event allowing for in-person or virtual participation. Mark your calenders. Registration will open by March 1.