Our Mission Statement

“To be the Premier Validation Firm offering Cost-effective, Regulatory Sound Approaches to Validation and Compliance.”

Operations Office

4770 N. Belleview Ave.
Suite 201
Kansas City, MO 64116
USA

Phone: 913-384-2221

Business

7930 W. Kenton Circle
Suite 140
Huntersville, NC 28078
USA

Phone: 704-230-4882

Validation
Qualification
Commissioning
Compliance

cGMP Validation was established in 1997 as a full service validation/compliance firm offering services for the pharmaceutical, bulk pharmaceutical, animal health, biotechnology, biologics, medical device and medical diagnostic industries.
cGMP Validation specializes in the preparation and execution of validation IQ/OQ/PQ protocols, compliance documentation for equipment, utilities, processes, laboratory instruments, and computer systems.
cGMP Validation has new and repeat clients across the United States, Puerto Rico and Canada. International experience includes projects in Egypt, Germany, Holland, Italy, Korea, Sweden, Indonesia, Vietnam, Singapore and Tunisia.
Corporate Office located in Kansas with Satellite offices in North Carolina, Pennsylvania, Maryland, California and New Jersey.

Services

  • Equipment
  • Utility Systems
  • Laboratory Systems
    Compliance
  • Processes
    Auditing, Risk Assessment, & Compliance Consulting
  • Educational Training Programs
  • Computer System Validation (CSV)
  • 21 CFR Part 11
  • Other Services

Our Mission Statement

“To be the Premier Validation Firm offering Cost-effective, Regulatory Sound Approaches to Validation and Compliance.”

Services

Equipment
Utility Systems
Laboratory Systems
Processes
Auditing, Risk Assessment & Regulatory Consulting
Educational Training Programs
Computer Validation
21 CFR Part 11
Other Services

Operations Office

4770 N. Belleview Ave.
Suite 201
Kansas City, MO 64116
USA

Phone: 913-384-2221

Business

7930 W. Kenton Circle
Suite 140
Huntersville, NC 28078
USA

Phone: 704-230-4882

Validation
Qualification
Commissioning
Compliance

cGMP Validation was established in 1997 as a full service validation/compliance firm offering services for the pharmaceutical, bulk pharmaceutical, animal health, biotechnology, biologics, medical device and medical diagnostic industries.
cGMP Validation specializes in the preparation and execution of validation IQ/OQ/PQ protocols, compliance documentation for equipment, utilities, processes, laboratory instruments, and computer systems.
cGMP Validation has new and repeat clients across the United States, Puerto Rico and Canada. International experience includes projects in Egypt, Germany, Holland, Italy, Korea, Sweden, Indonesia, Vietnam, Singapore and Tunisia.
Corporate Office located in Kansas with Satellite offices in North Carolina, Pennsylvania, Maryland, California and New Jersey.

Quality Assurance

A proven approach to validation and compliance that delivers work guaranteed to comply with the GMPs. Group activities are governed by…
More

Project Management
Effective on-site project management controls the scope and project costs, ensures reliable delivery of services, allows…
More
Team Approach

Validation and Compliance projects are staffed with consultants with considerable experience and diverse educational…
More