Appendix 1 - Common Acronyms - Guidelines for Reporting Adverse Events Associated with Vaccine Products - CCDR Volume 26S1 February 2000

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[Table of Contents]

Volume: 26S1 - February 2000

Guidelines for Reporting Adverse Events Associated with Vaccine Products
Supplementary guidelines for the Canadian Pharmaceutical Industry

Appendix 1 - Common Acronyms

ACCA	Advisory Committee on Causality Assessment
ADR	adverse drug reaction
AE	adverse event
ATI	Access to Information
CIOMS	Council for International Organizations of Medical Sciences
CPS	Canadian Paediatric Society
FDA	Food and Drug Administration - USA
ICH	International Conference on Harmonization
IND	Investigational New Drug
IMPACT	Immunization Monitoring Program ACTive
LCDC	Laboratory Centre for Disease Control
TPP	Therapeutic Products Programme
VAAEs	Vaccine Associated Adverse Events
VAAESS	Vaccine Associated Adverse Event Surveillance System
WHO	World Health Organization

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	Last Updated: 2002-11-08		Important Notices