Good Clinical Practice

Results with Integrity

Pharmatek’s team of highly qualified GCP auditors offers comprehensive auditing services tailored to your specific needs. Our experienced professionals have conducted audits across a wide range of therapeutic areas and clinical trial phases, ensuring compliance with international and national regulations.

With a global footprint and expertise in both on-site and remote auditing, our team can support your projects worldwide. We tailor our audit approach to each client’s needs. Our team develops a customized audit strategy that outlines the planning, preparation, execution, and reporting processes to meet your specific requirements. Rigorous peer review ensures that our audit outcomes meet the highest quality standards.

Whether you need general qualification, program-level, or study-level audits, Pharmatek’s expertise can help you achieve regulatory compliance and ensure the integrity of your clinical research.

Clinical audit services include:
Investigator Site Audits
Vendor Audits
Institutional Review Board (IRB) Audits
System / Process Audits
Central Lab Audits
Trail Master File Audits

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Our range of Clinical audit services include:

Vendor Audits

Qualification

Clinical Trail supply / Drug Depot

Systems Supporting Clinical Studies

Central Imaging Facility

Contract Research Organizations

Data Management

Biostatistics

Call Centers

Investigator Site Audits

Phase 1 to Phase IV Vendor Audits

Institutional Review Board (IRB) Audits

System / Process Audits

Electronic submission audits

Clinical operations & monitoring,

Data entry and & management

Statistical & Biostatistical department

Medical writing department

Central Lab Audits

Sample Management

Clinical Lab

Trail Master File Audits

Manual and Electronic TMF