This
web seminar will provide a general overview of the College of American
Pathologists (CAP) and Clinical Laboratory Improvements Amendments (CLIA)
requirements for laboratories that perform routine and non-routine testing of
clinical samples for clinical trials. We will review the laboratory
requirements for patient care and the requirements for clinical research.
Similarities and differences of CAP requirements from ISO 15189 Medical
Laboratories Requirements for Quality and Compliance, as applicable, will be
discussed. This web seminar provides training for the auditor/inspector
assessing clinical laboratories for compliance.
- Describe CAP/CLIA’s goals to patient safety and
privacy
- Describe the general CAP/CLIA
requirements
- Distinguish similarities and
differences of laboratory requirements from CAP and ISO 15189
- Identify inspection and/or audit a
laboratory’s compliance to CAP/CLIA
- Auditors
- Regulatory Agency Inspectors
- Laboratory Managers/Directors
- Laboratory Quality Professionals
Suzi Tran, M.B.A., CMQ/OE, CQA, CSQE
Click here for complete trainer
biographies
$835
Includes up to 20
participants at one site. All participants (up to 20) are eligible for
“Certificates of Attendance,” and accreditation, provided that accreditation
requirements are met. For groups larger than 20 or for additional sites, please
call +1 781.972.5400 or toll-free in the U.S. 800.856.2556 for pricing.
Barnett International is accredited by the
Accreditation Council for Pharmacy Education as a provider of continuing
pharmacy education. Participants will
receive 2 hours (0.2 CEUs) of continuing education credit for full
participation, including the completion of a pre-test, post-test, and program
evaluation. Barnett International will
issue a receipt of completion for earned CEUs within three weeks of program
completion. ACPE#: 0778-0000-17-078-L01-P.
Released: 2/17.
Hold
this course at your company! For more information, contact Naila Ganatra at +1
215.413.2471.
