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The Montrium blog

Your one-stop-shop for the most helpful and up-to-date ClinOps content written by our experts on the front lines of the life sciences industry.

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  • Validation
  • Validation
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  • Regulations & Standards

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  • Validation

The Roadmap to Validating Adobe Acrobat Sign for 21 CFR Part 11

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  • Validation
  • Quality

What’s in the FDA draft guidance on Computer Software Assurance (CSA)?

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  • Regulations & Standards

GAMP® 5 Second Edition: What you should know

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  • ClinOps

A reflection on the MHRA GCP Symposium: Trends that are transforming clinical trials

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  • Regulations & Standards

EU Regulation 536/2014: Everything You Need to Know, Simplified

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