Courses - Eventura.site

ICH Q7 – GMPs for Active Pharmaceutical Ingredients

3-Hour Virtual Seminar on Validation and Part 11 Compliance of Computer Systems

COMPUTER SYSTEM VALIDATION FOR CLOUD AND COTS APPLICATIONS

Artificial Intelligence in Pharmaceutical GMP Operations - Case Studies

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