Welcome to Compliance Media Inc.

We offer quality and compliance services for biopharmaceuticals and biomedical devices made under U.S. FDA, EU EMEA regulations for pharmaceutical and vaccines as well as ISO standards for medical devices. 

Our experts can help you efficiently assess, train and build quality systems for development, clinical trials and manufacturing. We can help you prepare for FDA and international inspections, provide quality assurance at your clinical sites, secure your supply chain, and meet the most stringent standards in the global marketplace for medical products.

We provide effective tools to bring innovative medicines to market faster, and in compliance with the highest standards for safety and effectiveness.

We provide expertise in: 

  • GMP Training and Auditing
  • GCP Training and Auditing
  • Supplier Qualification
  • FDA Audit Prep and 483 Responses
  • ISO13485 and QSR Internal Audits and Gap Analyses
  • Quality System Procedures
  • Product Investigations
  • Customer Complaints, MedWatch, and VAERS Reporting 
  • Regulatory Strategy and Regulatory Filings


Compliance Media/FDA PROS
Expert Guidance/Practical Training/Compliance Auditing

(650) 814-9562
Compliance Media Inc.
PO Box 60172
Palo Alto, CA 94306