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Best Practices Validation


Compliance, Risk Management & Validation Solutions for Life Sciences

  • Moving Compliance from "Burdensome Cost" to "Competitive Advantage"
  • Automating Validation Programs to Achieve the Highest ROI
  • Providing One System of Record for Real Time Data to Shorten FDA audits

As a thought leader in compliance for the Life Sciences industry, THINQ provides compliance solutions to a broad range of pharmaceutical,medical device and biotechnology companies. With a special expertise in validation, THINQ is now leading the way in changing how validation is managed in Life Sciences companies. Its leading edge validation software product called TCM is now enabling clients to automate their validation processes to plan, manage and measure their validation and risk compliance----no longer accepting validation as a cost burden that can not be tied to a company's overall market competitiveness.

In addition to the cost savings of automated validation, THINQ offers to clients best practices methodology, product training, prompt product installation and on going technical support. A customer achieves a permanent repository of real time retrievable validation data that is traceable to specific FDA regulations. TCM client users are able to set a high standard of compliance for their organization, pro-actively manage organization risk and provide prompt responses to satiate FDA audit inquiries.

The THINQ Compliance Experience

THINQ offers comprehensive compliance program development and management—powerful market-proven solutions, custom-tailored for our enterprise clients

  • Greatly reduce enterprise-wide risk and total cost of ownership
  • Leverage THINQ Compliance Manager (TCM), our flagship software solution that automates and streamlines crucial compliance, risk-mitigation and validation tasks
  • Create and maintain a real-time database of business-critical compliance content that can be generated on demand
  • Quality and compliance to COBIT, ITIL and GAMP standards
  • Hundreds of validation protocols delivered without a single negative audit (no 483’s!)
  • Automated testing
  • 20 years of compliance consulting expertise and experience deliver unrivalled peace of mind, quality advocacy and thought leadership