Courses - Eventura World us

How to go Paperless in an FDA-Regulated Environment using Electronic Workflow Signature Approvals and Electronic Records

OBJECTIONABLE MICROORGANISMS IN BIOPHARMACEUTICAL PRODUCTION – IDENTIFICATION AND RISK MITIGATION

OOS Test Results – Latest FDA Guidance

4-Hour Virtual Seminar on Project Management for Non-Project Managers

DATA INTEGRITY BY DESIGN, PHARMA 4.0 AND OVERCOMING DI ISSUES IN THE CLOUD

SDLC Modernization Continuous Quality in an FDA-Regulated Environment and Journey to Paperless SDLC/CSV

Preventive Maintenance and Calibrations – Regulatory Expectations and Best Practices

3-Hour Virtual Seminar on cGMP Regulatory Inspections – Through the Eyes of FDA, EMA and PMDA

4-Hours Virtual Seminar – Medical Device Cybersecurity and FDA Compliance

Steam Sterilization Microbiology and Autoclave Performance Qualification

Data Integrity and Privacy – compliance with 21 CFR Part 11, SaaS/Cloud, EU GDPR

Step-by-Step approach for Setting up FDA Audit Ready Quality Management System (QMS) – Case Studies based training