Courses - Eventura World

OOS And Setting Specifications For Pharma, Biopharma And Combination Products

21 CFR Part 11 Data Integrity Training For CSV, CSA, SaaS/Cloud - How To Reduce Costs For Compliance

Aseptic Processing and Validation Course

PROCESS VALIDATION TRAINING COURSE (FDA AND EU ANNEX 15: QUALIFICATIONS AND VALIDATION)

The eSTAR Submission Program For 510(K)S, IDES, DE NOVOS, PMAS, And Q-Submissions

GCP Risk Management And Risk-Based Monitoring

Preventive Maintenance And Calibrations - Regulatory Expectations And Best Practices

Design Control For Medical Devices And Combination Products

Process Validation Requirements And Compliance Strategies (Now In Spanish & English)

3-Hour Virtual Seminar on Successful Deviation Investigations

FDA'S Latest Guidance On Risk Evaluation And Mitigation Strategy (REMS)

Drug Master Files (DMFS) - Understanding And Meeting Your Global Regulatory And Processing Responsibilities

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