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Quality and Compliance Consulting, Inc.




Quality and Compliance Consulting, Inc. (QC2) provides worldwide audit and consulting services to the pharmaceutical, medical device, and biotechnology industries.  Founded in 1996, QC2 has conducted over 2,500 audits in 46 countries for more than 200 clients, ranging from small start-up to multinational pharmaceutical, medical device, and biotechnology companies, contract research organizations, bioanalytical and toxicology laboratories, institutional review boards, university and private medical research centers, and investigators.

Our expert staff will help you find practical solutions for regulatory compliance issues, develop and maintain quality systems, and ensure the validity and accuracy of your study data. In addition, our audits will assist you in assessing the adequacy of study conduct and compliance with FDA regulations and guidelines, ICH GCPs, local and international regulations, protocols, and SOPs.

Your company will benefit not only from our experience and expertise but also from the personal attention we give to each project and our dedication to providing high quality, cost-effect services.  

Our services include:


GCP Audits
Investigator Sites
Phase I Facilities and Studies
Institutional Review Boards
Essential Documents/Trial Master Files (TMF)
Electronic Trial Master Files (eTMF)
Data Listings
Clinical Trial Reports

GLP Audits
Toxicology Facilities and Studies
Formulation Analysis and Bioanalysis
Pathology Evaluations including Contracted Reading Vendors

Bioanalytical Laboratory Audits (GCP and GLP)
Large and Small Molecules

Clinical Pathology Laboratory Audits
Safety Panels
Flow Cytometry
Cell-Based Assays
Specialty Diagnostics

Sponsor, CRO, and Vendor Audits
Clinical Operations
Data Management and Biostatistics
Central Reading Centers
Electronic Data Capture (EDC)/Remote Data Capture (RDC)
Site Management Organizations
Safety Reporting

Computerized System Validation Audits
Data Management Systems including Electronic Data Capture (EDC)
Safety Databases
Electronic Patient Reported Outcomes Devices (ePROs)
Laboratory Information Management Systems (LIMS)

cGMP Audits
QC Laboratories
Investigational Product Packaging and Labeling Facilities

Standard Operating Procedures
Gap Analysis
Review and Revision


Audit Plan Development
Audit Follow-Up and Review of Corrective Actions
Preparation for FDA Inspections and Mock FDA Inspections
Patient Reported Outcomes (PRO) Consulting


Bioanalytical Data Audits/Laboratory & Validation Evaluation, Computer System Validation, Consulting, Contract Auditing, Data Validation, GCP Compliance, GLP Compliance, Quality Assurance/Control, Standard Operating Procedures, Training

Contact Information: 

Quality and Compliance Consulting, Inc.
409 West Olympic Blvd., Suite 708
Los Angeles, CA, 90015, USA
Phone : 4242083340
Fax : 8315155072
Internet : www.qc2.com
Email : qc2@qc2.com
Contact Person : Jason Bertram