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accorto regulatory solutions
  • Home
  • Solutions
    • Regulatory Strategy Development
    • Regulatory Due Diligence
    • Regulatory Submissions
      • Establishment Registration & Medical Device Listings
      • U.S. FDA 510(k)
      • De Novo Classification Requests
      • U.S. FDA Premarket Approval (PMA)
      • U.S. FDA Investigational New Drug Application (IND)
      • U.S. PMTA
      • U.S. Emergency Use Authorization (EUA)
    • cGMP Compliance & Audit Support
    • Regulatory Publishing
    • Post-Market Support
    • Clinical & Non-Clinical Studies
    • MoCRA
  • About
  • More
    • Careers
    • Events
    • FDA Changes in Motion
    • News & Insights
      • Become A Contributor
  • Contact Us
NewsletterBenjamin Mays2024-04-29T10:25:41-04:00

accortor regulatory solutions
Accorto Regulatory Solutions
14321 Winter Breeze Drive
Suite #196
Midlothian, VA 23113

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Solutions
Regulatory Strategy Development
Regulatory Submissions
cGMP Compliance & Audit Support
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Post Market Support
Clinical & Non-Clinical Studies
 
Submissions
US 510(K)
Establishment Registration & Medical Device Listings
Emergency Use Authorizations (EUAs)
De Novo Classification Requests
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Privacy Policy
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accortor regulatory solutions
Accorto Regulatory Solutions
14321 Winter Breeze Drive
Suite 196
Midlothian, VA 23113
Solutions

Regulatory Strategy Development
Regulatory Submissions
cGMP Compliance & Audit Support
Regulatory Publishing
Post Market Support
Clinical & Non-Clinical Studies
Regulatory Submissions

US 510(K)
Establishment Registration & Medical Device Listings
Emergency Use Authorizations (EUAs)
De Novo Classification Requests
US PMTA

Information
Cookie Policy
Privacy Policy
Terms and Conditions
News & Insights

Anything we can assist with?

Contact Us
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