Compliance Partner
Where Expertise Meets Excellence
FDA Quality and Regulatory Consultants (FDAQRC) is a leading provider of regulatory compliance solutions for pharmaceutical, biotech, and medical device companies globally. Our expert employees and consultants are experienced across all GxP areas to best suit client needs at all phases of product life cycle and development.
FDAQRC provides a range of services such as quality audits, mock inspections, gap assessments, remediation services, recruitment, and more. Through our global consultant network, we pair our clients with experts for every project, regardless of location. FDAQRC has around 500 active consultants in every major region (70+ countries). Our consultants go through an extensive vetting process, which allows us to personalize their consulting experience as well as ensure their expertise will align effectively with the specific requirements of each project.
✓ Global Regulatory Compliance Leader
✓ Expertise Across GxP Areas
✓ Comprehensive Services
✓ Advanced Consultant Network
✓ Personalized Consulting
✓ Excellence in Regulatory Compliance
✓ Tailored Solutions
✓ Client-Centric
✓ Trusted Partner
Setting the Standard in Global Quality & Regulatory Compliance
We excel in providing comprehensive support for projects in the realm of all GxP areas. We understand that your project’s needs may evolve, and we are ready to assist you at any stage of your journey. Below is a list of main categories in which we offer services, but our capabilities do go beyond this realm.
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Experts Across All GxPs
FDAQRC proudly boasts a global consultant network, demonstrating our dedication to top-tier service in quality and regulatory. With a decade of experience in 70+ countries, our powerhouse team covers all GxP areas, addressing diverse industry needs.
We take great care in selecting highly qualified individuals to join our esteemed network by following our stringent internal requirements for consultants.
˄ CONSULTANT QUICKLINKS ˄
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How To Find Qualified Patients for Your Clinical Trials
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Simplified Standard Operating Procedures Can Reduce FDA Citations and Enhance Compliance Culture
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Creating a Supportive Workplace: Recognizing and Addressing Mental Health
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AI in Clinical Trials: Transforming Research and Regulation
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FDAQRC's Retreat and Reconnect
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Pharmacovigilance: Insights, Challenges, and Future Horizons
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The Future Looks Bright
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