QTS, LLC
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    • Advanced Code of Federal Regulations
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    • Basic Environmental Monitoring
    • Basic Microbiology for the Life Sciences
    • Basics of Cell and Gene Therapy
    • Biologic GMPs
    • Chemisty Basics
    • Cosmetic GMPs
    • Disinfection and Sterilization Concepts
    • Downstream Processing Overview
    • Effective SOP Writing
    • Effective Technical Writing
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    • Freeze-Drying Fundamentals
    • Good Documentation Practices
    • HPLC in Theory and Practice
    • Laboratory Safety, Skills, and Ethics
    • Media Fill Basics
    • Medical Device GMPs
    • Pharmaceutical GMPs
    • Pharmaceutical Water Overview
    • Preparing for an FDA Audit
    • Quality Risk Management Concepts
    • Understanding and Implementing Annex 1
    • Upstream Processing Overview
    • Validation Fundamentals
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quality risk management overview

course description

Quality risk assessment is a regulatory responsibility for companies under regulatory jurisdiction. This six-hour course helps participants understand the risks that can adversely impact the product and the business operations, which is an important part of a company's quality system. The course also helps participants understand how to identify the risks associated with product quality and create strategies for mitigating these risks by identifying the root causes for subsequent corrective and preventative actions.
course specifics:
  • Participant Cap - 20
  • Delivery - Face-to-face or Virtual
  • Course Length - Four (4) hours
  • Printed Materials - Sent to company or college prior to delivery for them to print and disseminate
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