Past BACRR Events

Date Topic Speaker
12/07/09 Holiday Networking
10/26/09 Global Regulatory Strategy Regulatory's Piece of the Puzzle Meredith Brown-Tuttle
01/01/07 Test2 Test
02/17/06 Regulatory Intelligence Meredith Brown-Tuttle, RAC
12/01/05 Adverse Events in Clinical Trials Theresa Haedrich
09/27/05 Budget Development and Hidden Costs for Clinical Services Bonnie Wagner, MCCCM, BSc
05/06/05 ACRP Spring Networking Mixer & Panel Discussion on Independent Contracting Panel of 5 Clinical Research Consultants
04/28/05 Leadership Development and Life Balance Anne Moses, MSW, MBA, Certified Professional Coach
02/02/05 Introduction to HIPAA Electronic Record Security Regulations David Nettleton
12/15/04 Local FDA's Historical Perspective and Current Understanding of Clinical Sites and Sponsor FDA Audits Darlene Almogela, San Francisco District Supervisor, FDA
09/09/04 Clinical Investigative Site Budget Development and Negotiation Bruno Gagnon, B. Pharm., M.S. & Deborah Ovadia, M. S.
08/16/04 ACRP Summer Networking Mixer
07/21/04 BACRR Summer Networking Lunch Val Kenaley - Moderator
03/17/04 Investigational Site Quality: Signs and Symptoms of Questionable Compliance Liz Wool, RN,BN,CCRA & Greg Meyer, CQA, RAC
01/28/04 Implementation of the New EU Clinical Directive (Effective May 2004) with Specific Focus on Performing Clinical Research Work in the Netherlands Dick Veldhuis, PhD, Clinical Pharmacologist, Pharm
12/17/03 BACRR Holiday Networking Lunch
11/12/03 PreClinical Studies - What it takes to do In Vivo Studies from beginning to end James Swick, PhD, Chief Scientific Officer
09/09/03 Clinical Quality and Compliance; Systems, Planning, and Procedures Gregory A. Meyer RAC, CQA
08/18/03 FDA Concept Papers: Risk Management Sally Van Doren, PharmD
05/12/03 Latest 21 CFR Part 11 Guidelines and The 5 W's of Computer System Validation (Who, What, Where, When, Why...and Their Common Errors) David Nettleton
04/02/03 Establishing a SOP Administration Program at your Company: The Basics Liz Wool, RN, BSN, CCRA