About
What is VICH
Role of VICH
VICH Structure
VICH Process
What is the VICH Outreach Forum
Guidelines
General
Biologicals
Pharmaceuticals
Pharmacovigilance
Activities
Dates of next meetings
Dates of next Public conference
Public consultations
Library
Press releases
VICH Statements
VICH Steering Committee Minutes
VICH Outreach Forum minutes
Concept Papers
Procedural Guidance
Organisational documents (Priorities, Strategy and charter)
Conference documents archive
Other Documents
Training
General training material
Module 1 - General Topics
Module 2 - Quality
Module 3 - Efficacy
Module 4 - Safety
Module 5 - Biologicals
Module 6 - Pharmacovigilance
Contact
Members login
Remember me next time
I agree to the
privacy policy
Guidelines
Quality
Analytical validation
Impurities
Stability
Specifications
Safety
Environmental safety
Metabolism and residue kinetics
Toxicology
Target animal safety
Antimicrobial safety
Efficacy
Good clinical practice
Anthelmintics
Bioequivalence
Toxicology
Studies to evaluate the safety of residues of veterinary drugs in human food: Reproduction Testing
VICH GL22 (Safety: Reproduction) June 2001 - Implemented on 1 August 2002 - Revision 1 of May 2004
Studies to evaluate the safety of residues of veterinary drugs in human food: Genotoxicity Testing
VICH GL23(R) (Safety: Genotoxicity) October 2014 - Implemented in October 2015.
Studies to evaluate the safety of residues of veterinary drug in human food: carcinogenicity testing (Revision at Step 9)
VICH GL28 (Safety: Carcinogenicity) October 2004 - Implemented in March 2006
Studies to evaluate the safety of residues of veterinary drugs in human food: Repeat-dose (90 days) Toxicity Testing
VICH GL31 (Safety: Repeat-dose Toxicity) October 2002 - Implemented in October 2003 - Revison 1 of May 2004
Studies to evaluate the safety of residues of veterinary drugs in human food: Developmental Toxicity Testing
VICH GL32 (Safety: Developmental Toxicity) October 2002 - For implementation in October 2003 (Except EU: later date) - Revision 1 of May 2004
Studies to evaluate the safety of residues of veterinary drugs in human food: General Approach to Testing
VICH GL33 (Safety: General Approach) - Final Revision 2 at step 9 - Implemented in February 2010
Studies to evaluate the safety of residues of veterinary drugs in human food: Repeat-dose (chronic) toxicity testing
VICH GL37 (Safety: Repeat-dose chronic toxicity) May 2004 - Implemented in May 2005
Studies to Evaluate the Safety of Residues of Veterinary Drugs in Human Food: General Approach to Establish an Acute Reference Dose (ARfD)
VICH GL54 (Safety) November 2016 - For implementation by November 2017