Technical Expertise for Manufacturers of Pharmaceuticals and Biologics

Technical Expertise for Manufacturers
of Pharmaceuticals and Biologics

Validations

Validation is the cornerstone to the lifecycle of your products and manufacturing facility. Developed, executed and maintained correctly and pragmatically, it becomes a value-added system which establishes a firm foundation for ensuring product quality, safety, identity, strength, purity and efficacy. Our experience and expertise delivers to our clients the built-in quality practices which ultimately enables the facility processes, systems and people to perform in a continued state of control over the whole lifecycle.

We understand the current regulatory environment surrounding validation and validation support systems, having been leaders in successfully turning around sites under regulatory mandates.

Validation Services We Provide

Commissioning and Qualification

  • Engineering change management programs
  • Qualification process
  • Master Plan and Project Plan development
  • Critical Aspect Risk Assessments
  • Vendor/Service Provider Quality Assessments
  • Protocols, Reports, Validation Master Plans and Project Plans

Process and Cleaning Validation

  • All opportunities for matrixing and streamlining are taken while maintaining a compliant approach.
  • Ensure the processes have been fully proven and are repeatable, resulting in consistent products of high quality, safety, identity, strength, purity and efficacy.
  • Smoother, more contained regulatory interactions are realized since all the information and data are included in the studies.
Laboratory technician

Computerized Systems Validation

  • We ensure good data integrity practices across the board based on industry standard and recent regulatory actions related to Data Governance programs
  • Adherence to 21CFR Part 11
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