Courses - Eventura World us

Effective Design Control (21 CFR Part 820.30)

How to Prepare a 510(k) Submission

The DHF, Technical Documentation - Similarities, Differences and the Future

US FDA Drug Review and Approval Process

3-Hour Virtual Seminar on GAMP® 5 Second Edition – The changes and its impacts that you should know

Hypothesis Testing, P-Values, and Inference – When Thinking Like a Statistician Makes Sense

Risk Management using Lean – Are you sure your documents are clutter free?

Effective Design of Experiments (DOE) Strategies

3-Hours Virtual Seminar – Technical Writing for the Regulated Industries

Quality Risk Management Overview

Ensuring your Site is Ready for an FDA Inspection

Statistical Process Control (SPC) and Control Charts for Laboratory Compliance