FDA Warning

our approach

FDA Warning

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We've been in your shoes and understand the challenges you face.

Our team of seasoned subject matter experts, each with over 20 years of experience, provide tailored solutions for organizations of all sizes. At the core of our services is our proprietary AdaptiStrat® System, a cutting-edge approach designed to deliver lasting results and drive quality. By combining our consultants’ wealth of expertise with this innovative system, we are uniquely positioned to help clients achieve their goals and create a solid foundation for compliance and regulatory success.

What We Offer

Pre-Inspection Audits & Gap Assessments

  • Comprehensive FDA-style audits

  • Mock inspections (PAI, surveillance, for-cause)

  • Detailed gap analyses against FDA regulations (21 CFR Parts 210/211, 820, etc.)

  • Risk prioritization and remediation plans

Pre-Inspection Audits & Gap Assessments

  • Comprehensive FDA-style audits

  • Mock inspections (PAI, surveillance, for-cause)

  • Detailed gap analyses against FDA regulations (21 CFR Parts 210/211, 820, etc.)

  • Risk prioritization and remediation plans

Pre-Inspection Audits & Gap Assessments

  • Comprehensive FDA-style audits

  • Mock inspections (PAI, surveillance, for-cause)

  • Detailed gap analyses against FDA regulations (21 CFR Parts 210/211, 820, etc.)

  • Risk prioritization and remediation plans

Pre-Inspection Audits & Gap Assessments

  • Comprehensive FDA-style audits

  • Mock inspections (PAI, surveillance, for-cause)

  • Detailed gap analyses against FDA regulations (21 CFR Parts 210/211, 820, etc.)

  • Risk prioritization and remediation plans

Our Approach

We combine technical depth with real-world regulatory experience to ensure you’re inspection-ready—whether for GMP, GLP, GCP, or medical device compliance. Our team includes former FDA auditors and seasoned industry professionals who understand what regulators expect and how to deliver it.

Why FDA Warning Matters
  • Avoid costly delays in product approval

  • Reduce risk of 483s and Warning Letters

  • Improve operational transparency and compliance culture

  • Enhance trust with regulators, partners, and patients