The FDA and other regulators increasingly expect automation in quality and compliance. A case in point in your industry: Reporting adverse events electronically (eMDR) is mandated.
This e-Book will explore how the use of technology in the past decade or so has helped both regulated companies and regulatory agencies in easing the pains of delivering those products to patients and consumers worldwide. Regulatory milestones enforced by the FDA helped define the book’s scope.
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