Drug Development Meetings
Join FDAnews June 16 for a 90-minute audioconference on "Adverse Event Compliance in Clinical Trials: Know What to Report, When and How." Hear Mark Barnes, one of the world's most sought-after advisers on compliant clinical research programs, demystify adverse reporting for your clinical trials. On June 22, join FDAnews for "Root Cause Analysis: Understand Failures, Exceptions and Nonconformances." A veteran of hundreds of failure investigations will explain the fundamentals of developing, implementing and documenting an effective root cause analysis under your CAPA requirements.
May 30-June 1: Pharmaceutical Process Development
Amsterdam, Netherlands
(732) 238-1600
The Center for Professional Advancement
info@cfpa.com
www.cfpa.com
June 1-2: Drug Discovery and Development Asia-Pacific Congress
Singapore
(656) 835-5107
IBC Asia (S) Pte
lynn.ng@ibcasia.com.sg
www.ibc-asia.com
June 1-2: Pharmaceutical Technology Transfer
Amsterdam, Netherlands
(732) 238-1600
The Center for Professional Advancement
info@cfpa.com
www.cfpa.com
June 6-7: Pharmaceutical Risk Management
London, England
+44 207 647 2325
marcus evans Life Sciences
olas@marcusevansuk.com
www.melifesciences.com
June 6-7: Statistics 101: An Introduction to Statistical Principles and Thinking in Drug Development
Arlington, Va.
(703) 276-0178
Peri
maria.simonetti@peri.org
www.peri.org
June 6-8: TRAX -- Pharmaceutical Supply Chain Summit
Philadelphia, Pa.
(212) 661-3500 x3069
IIR USA
lyao@iirusa.com
www.traxsummit.com
June 8-9: The Drug Development Process -- From Discovery to Commercialization
Malvern, Pa.
(610) 688-1708
The Center for Professional Innovation & Education
info@cfpie.com
www.cfpie.com
June 8-10: Essential Training Course for New Clinical Statisticians
Arlington, Va.
(703) 276-0178
Peri
maria.simonetti@peri.org
www.peri.org
June 9-10: Stability Programs From Development to Approval
Malvern, Pa.
(610) 688-1708
The Center for Professional Innovation & Education
lcourville@cfpie.com
www.cfpie.com