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  Our Services  
   
  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"