Tuesday July 27, 2021 2:00-3:00pm Eastern
There is increasing adoption of circulating tumor DNA (ctDNA) assays in molecular oncology. Ensuring that technical and compliance requirements for clinical lab testing are met can be particularly challenging for ctDNA assays. This presentation will include discussion of analytical validation strategies for ctDNA assays to establish that assays perform as intended.
Learning Objectives:2. Understand challenges unique to cfDNA assay validation.
3. Identify solutions for analytically validating cfDNA assays.
4. Discuss opportunities and limitations for assessing circulating tumor DNA (ctDNA) in oncology.
Speaker: Christina Lockwood, MD |
Moderator: Meera Hameed, MD |
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- Log in using your AMP credentials. If you do not have an AMP account, create a FREE account by clicking here.
- Complete the Demographic questionnaire for the "Utility of Cell-Free DNA in the Clinic Series" before the webinar date. You will only need to do this once for the entire series.
Continuing Education Credit Information
CME credit: 1.0CMLE credit: 1.0
Last day to claim credit: August 27, 2021
Physicians (ACCME)
In support of improving patient care, this activity has been planned and implemented by Amedco LLC and the Association for Molecular Pathology. Amedco LLC is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.
Credit Designation Statement – Amedco LLC designates this live to enduring activity for a maximum of 8.00 AMA PRA Category 1 CreditsTM (1.00 CE for each webinar). Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Medical Laboratory Education (CMLE)
This activity has been planned and implemented in accordance with the Amedco and joint provider-ship of the ASC and the Association for Molecular Pathology (AMP). Course number 7013.
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