AIRB Training Workshops

AIRB believes that ongoing education and training is vital to advancing the highest standards in the conduction of clinical research trials.

AIRB understands that every research site has unique training requirements and we will customize your workshop to best meet your needs.

Who should attend? Clinical Research Personnel CRCs Principal Investigators CRAs Project Managers Clinical Study Managers from clinical research organizations, research centers and sponsor companies

Affordable training for your staff 1.5 CEU's available per workshop session Latest information on regulatory requirements and newest advances.

Description of Workshop Sessions Session 1 - The History of the IRB and Principles of Good Clinical Practices Session 2 - The Process of Informed Consent Session 3 - Are You Ready For An Audit? Session 4 - Science, Technology, and Marketing; the New Expectations for CRCs and CRAs Session 5 - Good Clinical Practices for Principal Investigators

For more information and fees contact: Cynthia Owens or Richard Clunie at 978-462-6415 or e-mail Cynthia Owens, MA, CRCC, is a co-founder of AIRB, and owns and operates a national research consulting service, Pharmsight. She has written and implemented SOPs, recruitment plans, staff training manuals, and quality assurance guidelines, as well developed and taught educational programs for hospitals. A featured speaker at national symposiums on good clinical practice, Cynthia is recognized as a leader in her field.