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GCP Audits, Training, Investigator Site and Part 11 Compliance Assessments

The Clinical Services Group

Full Service Clinical Management Organization

Clinical Audits, Site Training and Monitoring
Pharmaceuticals and Medical Devices

GCP  -  GCLP  -  CRO Audits

Clinical Audits and Training
Good Clinical Practice (GCP)
CRO Audits - Investigator Site Audits
GMP Audits and Training for the Drug, Medical Device, Dietary Supplements and Cosmetics industry
Good Clinical Laborataory Practice (GCLP)
Small Molecule - Toxicology - Tissue
GMP Audits and Training for the Drug, Medical Device, Dietary Supplements and Cosmetics industry
Good Manufacturing Practice (GMP)
For Clinical Investigational Products
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Good Storage & Distribution Practice
Stability Management
  • We Audit the Regulations
  • We Print the Regulations
  • We Know the Regulations
Clinical Audits and Training
GMP Audits and Training for the Drug, Medical Device, Dietary Supplements and Cosmetics industry
GCP Training & Site Monitoring
GMP Audits and Training for the Drug, Medical Device, Dietary Supplements and Cosmetics industry
Good Clinical Study Management
IND, NDA, PMA, 510k, BLA
Feasibility, Phase I - II - III - IV Studies
Medical Device Audits and Training
Clinical Audits and Training
21 CFR Part 11 Compliance
Data Management & Data Integrity

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The Auditing Group Clinical SMEs have extensive experience, with Pharmaceuticals, Biologics, & Medical Devices (and Combination Devices), to ensure a successful registration process. 

A Clinical Auditor / SME will Respond!

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