Pharmaceutical Validation

Validation is establishing documented evidence for demonstrating that a procedure, process, and activity will consistently lead to the expected results. It often includes the qualification of systems and equipment. It is a requirement for Good Manufacturing Practices and other regulatory requirements. FDA has issued guidance to the industry so that they can benefit from products and processes which are both stable and predictable.

How Can TAKE Solutions Help?

TAKE’s Validation Consulting team can provide experienced QA Specialists performing Quality Assurance services tailored to your needs at low cost, and in a time-efficient manner. The team carries over 20 years of experience, a proven success rate, and many satisfied global customers.

Products/Services

• Software Validation
• Equipment Validation
• Test Method Validation Documentation
• SOP and other Documentation Writing
• QA Audit Readiness