Courses - Eventura World

FDA Regulations for Environmental Monitoring (EM) Program

MDSAP Audits – All You Need to Know

FDA Case Scenarios – Best Practices for Managing Inspection Situations

Qualification and Control of Contract Manufacturer Organizations Based on Practical Experience

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