Courses - Eventura.site

Project Management Best Practices For Computer Systems Regulated By FDA

The US FDA QMSR Transition - 21 CFR 820 And ISO 13485

FDA Regulated Mobile Medical Apps as Devices And Cybersecurity Explained

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

Preventive Maintenance And Calibrations - Regulatory Expectations And Best Practices

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)

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