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  • Courses
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    • By Category
      • Clinical Trials
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      • R&D
      • Leadership & Training
    • Meet the Instructors
  • Blog & Resources
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Research & Development

  • $279
    Process Validation: Ensuring Compliance With Multiple Standards
     
    On-demand
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  • $279
    Project Management: Best Practices for Validation & Regulatory Projects
    Bruce Fieggen
    On-demand
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  • $279
    Quality Assurance and Quality Control – Differences in FDA vs. EU Regulations
    Thomas Pritchett
    On-demand
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  • $279
    Regenerative Medicine: Understanding the Regulatory Landscape
    Kelly Lightfoot, Andrew Ittleman
    On-demand
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  • $279
    Renovating Pharmaceutical Manufacturing Facilities for Aseptic Fill/Finish: Critical Planning, Execution & Compliance Tips
    Erich Bozenhardt, Herman Bozenhardt
    On-Demand
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  • $279
    Stability Programs – Key Factors in Meeting FDA/ICH Expectations
    Judy Carmody
    On-Demand
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  • $279
    Surviving an FDA Good Laboratory Practices (GLP) Inspection – Critical Tips For Compliance
    Michael Hamrell
    On-demand
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  • $279
    The Top Method Validation Mistakes – And How to Avoid Them
    Judy Carmody
    On-Demand
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  • $279
    Top IND Pitfalls & How to Avoid Them
    Samantha Zappia
    On-demand
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CATEGORIES

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TOPICS

Cleaning ValidationCleanroomClinical TrialsCloudCMOsComputer SystemsCRAsCROsData IntegrityDeviceeCTDEHRsEMAEquipmentFacilitiesFDAGCPGDPGLPGMPHIPAAHuman ErrorICHInformed ConsentInspectionsInstructional DesignManagementmanufacturingMarketingMDRmicrobial controlProcess ValidationProject ManagementQualityQuality by DesignQuality Risk ManagementRemote MonitoringRiskRisk-Based MonitoringRoot Cause AnalysisSite MonitoringSOPsTrainingTrial Master FileUpcoming Courses

Your Courses

Upcoming Live Courses

  • Clinical Quality Management Systems (QMS): Establishing A Practical & Compliant Program
  • Establishing Appropriate Quality Metrics
  • Executing Proper Event Investigations: Critical Steps In Ensuring Compliant Corrective Actions
  • Use of Electronic Records and Electronic Signatures in Clinical Investigations Under 21 CFR Part 11
  • cGMP Compliance - Understanding The Top Drug Enforcement Trends
  • CAPA and Root Cause Analysis: Essentials Post ICH GCP E6 (R2) Addendum
  • ICH E6 Addendum R2 Team Training and Action Planning

About

The Life Science Training Institute helps pharma, biotech, and medical device companies build knowledgeable, compliant workforces by providing training from drug discovery through commercialization.

We are dedicated to advancing careers of those working to develop new therapies and to protect patient safety.

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Contact

  • 101 Gibraltar Road, Suite 100. Horsham, PA 19044
  • 215-675-1800 (option 3)
  • info@lifesciencetraininginstitute.com

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