It is no secret that adopting new software in organizations that must adhere to FDA regulations is extremely challenging. Multiple steps must be performed before the users in an organization can start using the new software. For example, vendor validation and creating new SOPs are some of the challenging hurdles for adopting a new Electronic Lab Notebook.

When adopting LabLog, you can request the assistance of our in-house team of regulatory experts. Our experts can help you set up the correct documentation for validation. We can also help with creating SOPs, and performing impartial audits after implementation.

We have already verified that LabLog is compliant with FDA Part 11. We can therefore provide all necessary documents required for validation and auditing.

Read our blog posts on FDA compliance to learn more:

  1. The All-In-One Solution for FDA Electronic Records Compliance
  2. 7 Ways to Become FDA Part 11 Compliant Without Spending a Dime
  3. 5 Facts About FDA Compliance Of Digital Lab Notebooks

For an in-depth analysis of LabLog's compliance to FDA download our white paper or request a 1:1 live demo.

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