Triveritas
can assist you in achieving compliance to current quality standards
for pre-clinical and clinical veterinary trials in Europe and beyond.
We
can provide excellence and experience in Quality Assurance (QA),
an essential ingredient of product development, whether in pre-clinical
studies, clinical trials or manufacturing. We are available for
QA monitoring and facility audits to the principles of Good Laboratory
Practice (GLP), Good Clinical Practice - veterinary (GCPv) and Good
Manufacturing Practice (GMP).
GLP,
GCPv and GMP facility inspections.
GLP
and GCPv study inspections.
Study
plan and protocol reviews.
Sponsor
trial master file audits.
GLP/GCPv
report audits.
Training
of QA personnel.
GLP/GCPv
training for non-QA personnel.
Liaison
with, and inspection of, contract research facilities.
QA
support.
GLP
and GCPv implementation.
Independent,periodic
review of QA functions and procedures.
Compilation
of Standard Operating Procedures and policies.