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…
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Project Management
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Team Approach
Validation and Compliance projects are staffed with consultants with considerable experience and diverse educational…
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