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  • Combination Products
  • Pharma/Biopharma
  • Quality Management
  • Food Safety Management
  • Soft Skills
  • Effective Technical Writing Skills
  • Creating High-Quality Products: A Training Course for Manufacturing Professionals
  • 5S Training Course
  • Creative Problem Solving: Unlocking Innovation in Production Operations
  • Mistake Proofing (Poka Yoke) Training
  • Failure Mode and Effect Analysis (FMEA)
  • Medical Device Micro-Training Courses
  • Quality Systems
  • CAPA
  • EU MDR
  • Audit preparation
  • Risk Management
  • ISO 13485:2016 Clause by Clause
  • Introduction to 21 CFR 820 Quality System
  • CAPA in the Medical Device Industry
  • Project Management Skills for an Effective CAPA
  • Mastering EU MDR: Navigating Compliance for Medical Devices
  • How to Prepare for a FDA QSIT Inspection
  • How to Prepare for a Medical Device Single Audit Program (MDSAP)
  • ISO 14971:2019 Risk Management for Medical Devices Classroom Training
  • Annual cGMP Drug/Device Combination Products (21 CFR 820, ISO 13485:2016, CFR Part 4, 210 and 211)
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  • FDA QSR & QSIT for Medical Devices: An Introductory Course
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  • Introduction to ISO 14971:2019 Risk Management for Medical Devices Training Course
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