Triveritas can assist you in achieving compliance to current quality standards relating to all aspects of veterinary product development and production.
We can provide excellence and practical advice in Quality Assurance (QA), an essential element of product development, whether in pre-clinical studies, clinical studies, pharmacovigilance or manufacturing.
Our trained QA auditors are experienced in auditing to the principles of Good Laboratory Practice (GLP), VICH Good Clinical Practice (VICH GCP) and Good Manufacturing Practice (GMP), compiling audit reports and following up recommendations.
Amongst the services we offer are:
- facility inspections
- manufacturing site inspections
- study plan and protocol reviews
- in-phase inspections of GLP and VICH GCP studies
- pharmacovigilance system audits
- process audits
- data and Study Master File audits
- GLP and VICH GCP report audits
- training of QA and non-QA personnel
- GLP and VICH GCP implementation
- QA support
- independent review of QA functions and procedures
- compilation of Standard Operating Procedures and policies
