We provide a full spectrum of professionals for
Quality Assurance, Validation, GxP Auditing and Analytics. One
of our lead consultant Holds six certifications from the American
Society for Quality and have served as a Subject Matter Expert
to this organization in the field of biomedical auditing.
We have successfully assisted many companies with high-level appointments
in Manufacturing Quality (GMP) and Clinical Compliance (GCP) for both long-term
and permanent positions.
Our Quality resourcing team has assisted manufacturing sites for Small
Molecule and Biologics for Approved Manufacture QA and Release as well
as Clinical Supply (IMP). Our areas of coverage and assignment take-up
include:-
Site and Corporate Heads of Quality Assurance,
Qualified Persons (QPs) and Compliance Managers,
GMP & ISO Manufacturing Site Auditors,
Validation Managers and Specialists (Equipment Qualification
and Software),
Methods Development, Analytics and Quality Control Officers,
SOP and GMP Documentation Specialists.
For Clinical Compliance in
GCP, we have provided experienced personnel to both Pharmaceutical
and Clinical Research Organisations. We have completed many
assignments for GCP in the USA, providing:-
US FDA experienced VPs and Directors of Regulatory Compliance;
Associate Directors and Managers of Clinical Quality Assurance;
Senior GCP Auditors and GCP Auditors;
Interim GCP Auditors for long-term assignment’s (minimum
three months).
Our team for Quality resourcing is well-known for
speed of delivery, priding ourselves on the motto of "bringing
Quality people together"
