Our full-service practice provides high-quality consulting services to clients from the pharmaceutical and medical device industries. Our action-biased professionals help clients achieve success, completing projects on time and within budget with a focus on sustainable compliance.
Below is a partial list of our offerings:
- Compliance Assessment and Remediation
- Design Review / Design Qualification
- Process Risk Analysis and Mitigation Strategy Development
- Validation Master Planning
- Sterility Assurance Planning and Execution
- Validation Life Cycle Documentation Generation, Review and/or Remediation
- Commissioning & Qualification of Equipment and Facilities
- Process Validation
- Computer System Validation
- Aseptic Process Evaluation and Remediation
- Quality System Development and Deployment
- 483 response strategy and action
- Vendor Qualification
- GxP Technical Staffing Solutions
- US Agent - FDA
- cGMP Training
- Project Management
For additional information or to request a proposal please contact us.
Compass Technical Group, Inc.
Office: (636) 352-2033
Fax: (636) 246-0266
copyright 2009-2012 Compass Technical Group, Inc. All rights reserved