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Certificate

Pharmaceutical Cleaning Validation

Program code:

Credential:

Certificate

Duration:

Delivery Mode:

Start Date(s):

January | May | September
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The cleaning of facilities and equipment is a critical activity to avoid contamination and cross-contamination. Hence, experts in Pharmaceutical Cleaning Validation are in high demand. This training focuses on the cleaning and sanitation procedures that need to be validated to demonstrate effective cleaning and sanitation programs for facilities, utilities, equipment, and health and hygienic practices.

Anyone who wants to become a Validation Specialist/Scientist/Engineer, Validation Associate, Production Personnel, Technical Team Member, Management Team Member, or Auditor should attend the Pharmaceutical Cleaning Validation program.

Learning Outcomes

After successful completion of this course, students will be:

  • Able to understand current cleaning and sterile validation regulatory requirements
  • Understand the benefits of cleaning/sterile validation
  • Develop sanitation SOPs
  • Select and implement different types of cleaning/sterile validation approaches
  • Write cleaning/sterile protocols and validation plans
  • Perform risk analysis
  • Perform continuous cleaning/sterile process improvements

  • Module 1: Pharmaceutical Sanitation Programs
    • Generic Sanitation Program
    • Sanitation Validation/Verification
    • Cleaning Validation Requirements
  • Module 2: Pre-operational Sanitation Assessment
    • Operational Sanitary Practices
    • Personnel Health and Hygiene
    • Premises Sanitation Requirements
  • Module 3: Sterile Validation
    • Types of Sterilization
    • Process Controls
    • CIP/SIP
  • Module 4: Cleaning Verification and Cleaning Validation
    • Cleaning Master Validation Plan
  • Module 5: Preparing for Cleaning Validation
    • Process Controls
    • Writing Cleaning Validation Protocol
    • Writing Cleaning Validation Report
    • Case Study
  • Module 6: Effective Sanitation Program
    • Gap Analysis
    • Dirty Hold Time Studies
    • Clean Hold Time Studies
    • Deviations/CAPA/Change Control
  • Module 7: Writing Cleaning Validation Protocol
    • Writing Cleaning Validation Report
    • Case Study

Who Should Attend

Anyone who wants to become the following should attend this webinar on pharma cleaning validation:

  • Validation Specialist / Scientist / Engineer
  • Validation Associates
  • Production Personnel
  • Technical Team Members
  • Management Teams
  • Auditors
  • Validation Assistant
  • Validation Specialists
  • Coordinators
  • Managers