Courses #FDA - Eventura World us

ESSENTIAL EU MDR REQUIREMENTS - MINIMIZE THE RISK OF NON-COMPLIANCE

3-HOUR VIRTUAL SEMINAR ON 510(K)'S, PMA'S, IDE'S AND DENOVO'S

Establishing FDA-Compliant Product Stability Testing Program

FDA Expectations for 505(b)(2) Regulatory Pathway for New Drugs

FDA vs Health Canada - Similarities and Differences between the two Regulatory Bodies

FDA/ICH Guideline Q9 (R1) On Quality Risk Management

3-Hour Virtual Seminar On IEC 62304 - Medical Device Software Compliance

Quality in Technology Transfer Projects

4-HOUR VIRTUAL SEMINAR ON CHANGE CONTROL ACCORDING TO GXP AND GMP REQUIREMENTS

Handling Out-of-Trend Results in Pharmaceutical Quality Control as per Latest FDA Requirements

FDA Regulations for Environmental Monitoring (EM) Program

MDSAP Audits – All You Need to Know

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