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2020-2021 Cyto-econference Webinar Series
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2020-2021 Cyto-econference Webinar Series

Live Cyto-econference webinars connect you to the presentation in real time, including a question and answer session, interactive polling and access to online reference materials and tools. Archived webinars are recordings of the live presentation, giving you the flexibility of viewing the activity online or on your mobile device. Archives are a great way to get credits “on the go” on the topics of your choice.

 Export to Your Calendar 4/28/2020 to 3/23/2021
When: Tuesday, April 28, 2020
Where: United States
Contact: JoAnn Jenkins
(302) 543-6583 ext 103


Online registration is closed.
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Do you find rapid on-site evaluation using modified Giemsa stains difficult? Are rapid on-site evaluations in the bronchoscopy suite a new or continuing part of your practice? This webinar will provide participants an opportunity to understand issues surrounding appropriate specimen triage, and highlight some of the pitfalls on EBUS rapid on-site evaluations. EBUS-guided FNA cases will be reviewed with audience polling during the webinar, with each case demonstrating a particular focus in regard to optimizing patient care.

Live Cyto-econference webinars connect you to the presentation in real time, including a question and answer session, interactive polling and access to online reference materials and tools. Archived webinars are recordings of the live presentation, giving you the flexibility of viewing the activity online or on your
mobile device. Archives are a great way to get credits “on the go” on the topics of your choice.

Purchasing any live webinar will give access to the archived event online or on your mobile device.

Educational Objectives
At the completion of this activity, participants should be able to:

  • Understand the recent standardized terminology system: The International System for Reporting Serous Fluid Cytopathology
  • Recognize urinary tract cytopathology specimens that are a challenge to the Paris System
  • Review cytomorphologic features of salivary gland tumors
  • Understand HPV testing and quality assurance in GYN cytology
  • Evaluate and assess small samples of the lung and mediastinum
  • Review the new ASCCP risk-based consensus guidelines for cervical cancer
  • Discuss the role of the cytopathologist in the genomics laboratory
  • Understand the importance of Quality Assurance (QA) and Quality Control (QC) in a cytopathology laboratory through validation, billing and coding
  • Recognize common and uncommon tumors of the kidney
  • Understand the application of ROSE in the bronchoscopy suite

Continuing Medical Education (CME)
The American Society of Cytopathology is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.

The American Society of Cytopathology designates this live and enduring educational activity for a maximum of 24 AMA PRA Category 1 Credits™. Physicians should only claim credit commensurate with the extent of their participation in the activity.

American Board of Pathology Continuing Certification (CC)
This product can help fulfill the CME requirements and Self-Assessment Modules (SAMs) mandated by the American Board of Pathology Continuing Certification (CC) process.

Continuing Medical Laboratory Education (CMLE)
The ASC designates these activities for the indicated number of Continuing Medical Laboratory Education (CMLE) credit hours.

This program is approved for 24 continuing education credits in the State of Florida and 12 in the State of California.

The credit on each webinar is good for three years from the live presentation date.

100 West 10th Street, Suite 605 Wilmington, Delaware 19801302-543-6583302-543-6597
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