Courses #2 Days - Eventura World

Annual GMP Masterclass for 2024

The FDA QMSR And The Key Elements Of QSIT cGMP Inspection And Audits For Medical Device Manufacturers

Statistical Elements Of Implementing ICH Quality Guidelines

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)

SOP Synergy 2024

FDA Inspections and Audit Readiness Course

Enhancing Quality Oversight In Pharmaceutical Contract Manufacturing Organizations

AUDIT LIKE THE FDA - EFFECTIVE INTERNAL AUDIT PROGRAM

Death by CAPA - Does your CAPA Program need a CAPA?

COMPLAINT HANDLING, MEDICAL DEVICE REPORTING AND RECALLS - POST-MARKET REGULATIONS TRAINING