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  • Courses
    • All Courses
    • Upcoming Live Courses
    • By Category
      • Clinical Trials
      • Manufacturing
      • Med Device
      • Regulatory
      • R&D
      • Leadership & Training
    • Meet the Instructors
  • Blog & Resources
  • About Us
    • About LSTI
    • Enterprise Solutions
      • CRA Academy
      • GxP Refresher Courses
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    • Contact Us
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  • View Cart
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On Demand Courses

  • $279
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    Aseptic Process Simulations – A Comprehensive Guide for Proper Execution
    Danielle DeLucy
    On-Demand
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  • $199
    Building a Best in Class Medical Affairs Organization: Strategies for Success
    Judith Serafin
    On-Demand
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  • $279
    cGMP Compliance – Understanding The Top Drug Enforcement Trends
    Joanna Gallant
    On-Demand
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  • $279
    Data Integrity: Why Not Identifying Repeat Defects In Your Data Is Killing Your Performance
    Ben Locwin
    On-Demand
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  • $279
    Electronic Document Management Systems (EDMS) And Electronic Common Technical Documents (eCTD) – An Overview
    Daniel Orfe, Betsy Fallen
    On-demand
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  • $279
    FDA Regulations for Analytical Instrument Qualification and Validation: Comprehensive Best Practices
    Joy McElroy
    On-Demand
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  • $279
    Implementing the ASTM E2500 Validation Method: 10 Years of Key Learnings
    Rich Yeaton, Kelly Thomas
    On-Demand
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  • $279
    knowledge transfer
    Improving Product Quality During Technical Transfer – Minimizing Risk, Maximizing Results
    Eric Good
    On-Demand
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  • $279
    Key Elements of Pharmaceutical Serialization and Track & Trace Systems: Implementation and Compliance Best Practices
    Terry DeMarco
    On-Demand
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CATEGORIES

  • Clinical Trials (86)
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  • Med Device (51)
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  • IT & Data (27)
  • Upcoming Live Courses (17)
  • On Demand Courses (190)
  • Introductory Courses (20)
  • Special Packages (5)

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

  • The EU General Data Protection Regulation (GDPR): What US Companies Need To Know To Comply
  • The Core Competencies of a World-Class Medical Affairs Team
  • Executing Proper Event Investigations: Critical Steps In Ensuring Compliant Corrective Actions
  • FDA Guidance for Industry "Process Validation: General Principles & Practices" – Whatever Happened to IQ, OQ, PQ?
  • Measuring CAPA Effectiveness: Critical Tips in Getting the Right CAPA and Showing It Works
  • Biocontainment For Manufacturing: Understanding The Risks, Guidance, and Design Requirements
  • Right to Try Legislation: Impact on Industry, Health Authorities, and Patients

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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