Validation, Commissioning & Qualification
Reliant’s consultants offer a full range of validation services for highly regulated industries, including pharmaceutical and medical device manufacturers. We can assess your existing validation process or implement a new validation solution to meet your specific requirements.

We specialize in commissioning, qualification, and validation, and our experienced team combines comprehensive compliance and technical knowledge to efficiently develop and execute project plans and solutions that address the individual needs of each of our clients.


  • Process Validation
  • Cleaning and Sterilization Validation
  • Shipping validation
  • Equipment, Utilities, and Facilities Validation
  • Computer System Validation
  • Commissioning protocol development and field execution
  • IQ/OQ/PQ protocol development and execution
  • Automation qualification
  • FAT/SAT planning and execution support
  • Facility and process startup support
  • Good Manufacturing Practices (GMP) Product
  • Lifecycle Methods
  • Design review and qualification

Reliant can offer a scalable turn-key solution and services that will support and enable startups, spinoffs, small and medium-sized medical device companies to comply with the new regulations listed above. We are ready to support the new quality and regulatory requirements that must be met throughout the medical device lifecycle.

We would love to hear from you.

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A team of experts on a mission
We’re a staffing company. Sure. But it’s the desire to do things better that drives us. We’re smaller, and we love it! We get to spend our time investing in relationships.