­čôł Labeling Maturity Assessment ÔÇô How do you stack up? Take Assessment

Skontaktuj si─Ö z nami
Przegl─ůd produkt├│w

September 28, 2022

Report

Ensuring FDA Compliance: The Essential Guide to FDA 21 CFR Part 11

FDA 21 CFR Part 11 allows Medical Device and Life Science organizations to use electronic records and signatures in place of paper. This helps organizations reduce the cost of managing and documenting their entire labeling lifecycle, from routing and approval workflow, version control and comparison, to audit trails and reports.

Wondering how to get started on the path to compliance? A good first step is to read our ÔÇťEnsuring FDA Compliance: The Essential Guide to FDA 21 CFR Part 11ÔÇŁ whitepaper. In this paper, we discuss the eight phases of FDA 21 CFR Part 11 compliance and what it means to the labeling lifecycle.

  • Regulatory
  • FDA
  • Labeling

Thank you! You can read the paper here: [[PDF]]

Multiple or single choice

For additional details see the Loftware Privacy Policy

For additional details see the Loftware Privacy Policy