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      • "The Validation Master Plan: How to Write It and How to Make it Work for You"
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      • Introduction to Design Control
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    • What are cGMPs?
    • What is Change Control?
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    • Cultural Transformation
    • What are Design Controls?
      • Introduction to Design Control
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    • What is a Gap Analysis?
    • What are GLPs?
    • What are QSRs?
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    • What is a Drug Pedigree?
      • Article on Drug Pedigrees in Pharmaceutical Engineering
    • What is Risk Management?
      • characterization
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  • Training Services
    • Training Seminars
      • Conducting Effective Audits
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      • cGMP Training Basics for Production personnel, Review
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      • cGMP's for QC/QA, Review
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      • Introduction to Basic QSRs
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      • Validation Training: Analytical Methods
      • Validation Training: An Introduction to IQ, OQ, and PQ
      • Validation Training: A Practical Application of Qualification Principles
      • Validation Training: Executive Briefing
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      • Microbial Control and Validation
      • FDA Inspections: How to be prepared
      • Good Documentation Practices
      • Writing Compliant, Practical Standard Operating Procedures (SOP's)
      • Filling in Batch Records
      • Corrective Action Preventive Action (CAPA)
      • Deviation Control
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      • Out of Specification Results
      • Failure Investigations (under construction)
      • Manufacturing and the Quality Within
      • Manufacturing and Quality: a Partnership for Success
      • The Production Employee's Role in Microbiological Control
      • Change in the Workplace
      • Effective Project Management
      • Leadership Skills for a Regulated Environment
      • The Foundation of High Performance Teams
      • Cultural Transformation
    • e-Learning
      • Introductory cGMP Training (details)
      • Introductory cGMP Training - BUY
      • Corrective and Preventive Action / Root Cause Analysis (details)
      • Corrective and Preventive Action/ Root Cause Analysis - BUY
      • Introduction to Medical Device Approval Pathways (details)
      • Introduction to Medical Device Approval Pathways - BUY
      • cGMPs for Drugs and Finished Pharmaceuticals (details)
      • cGMPs for Drugs and Finished Pharmaceuticals - BUY
      • cGMPs for Pharmaceutical Operations Personnel (details)
      • cGMPs for Pharmaceutical Operations Personnel - BUY
      • Calibration for FDA Regulated Industries (details)
      • Calibration for FDA Regulated Industries - BUY
      • Quick facts about VCI's e-Learning Curriculum
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      • Free Sample! (Course Details)
  • What is Validation?
    • Validation Master Plan
    • Process Validation
    • Process Characterization
    • Computer and Automated Controls Validation
    • 21 CFR Part 11, Electronic Signatures, Electronic Records
    • Laboratory Validation
    • Cleaning Validation
    • HACCP: Hazard Analysis and Critical Control Points
  • Industries
    • Dietary Supplements
      • Training on 21 CFR 111
      • Dietary Supplement Regulations: What You Need to Know
    • Food
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      • Validation
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      • Audits and Gap Analysis
      • Validation Master Plans
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      • Compliance Services Page
    • Pharmaceuticals
      • Process Validation
      • Analytical Method Validation
      • Drug Master Files
      • Risk Management (ISO 14971)
      • Compliance
      • Training
      • Quality Systems Design and Compliance Upgrade Projects
      • Audits and Gap Analysis
      • Validation Master Plans
      • Equipment Qualification and Process Validation
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  • Article Archives
    • Validation & Compliance Institute Provides Regulatory Training for SIMCO Electronics
    • MichBio Members Now Save on Validation & Compliance Institute Services
    • VCI's Good Manufacturing Practices Certification is in Great Demand
    • VCI to Provide Medical Device Regulatory Training for the University of Michigan's Medical Innovation
    • Alternatives for Container and Closure Systems Sterility Testing
    • Drug Pedigrees: Your Supply Chain Needs Them. Are You Ready?
    • Dietary Supplement Regulations: What You Need to Know
    • Evolution of Validation
    • FDA's New Process Validation Guidance Recommends Team Approach
    • Five Ways to Accelerate Root Cause Investigations
    • Food Recalls and Mislabeling: How to Avoid Mistakes Before Products Hit the Shelves
    • How to Evaluate the Quality of a Dietary Supplement
    • How to Get Your Project Approved
    • Labeling Errors Make Recalls Likely
    • The Myth of the Generic SOP
    • A New Paradigm to Address the High Cost of Vendor Qualification
    • Off-Label Use of Medical Devices
    • Quality by Design Streamlines Pharmaceutical Manufacturing
    • Relief for Latex Allery Sufferers as FDA Clears New Medical Glove
    • Two Profound Facts about Employee Performance
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