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Life Science Training Institute
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    • Live Courses/Webinars
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      • Clinical Trials (GCP)
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      • DIGR-ACT: Critical Thinking Skills for Clinical Trials
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  • WEBINARS/eLEARNING
    • Live Courses/Webinars
    • On-Demand Courses/Webinars
    • By Category
      • Clinical Trials (GCP)
      • Manufacturing
      • Medical Devices
      • Regulatory
      • R&D
      • Leadership & Training
    • eLearning
      • Clinical Pathways
      • DIGR-ACT: Critical Thinking Skills for Clinical Trials
    • LSTI Learning Library
    • Training Voucher Packages
    • Checkout
  • Custom Training
    • Live Training
    • Elearning Solutions
    • LSTI Corporate Learning Library
    • CRA Academy
  • Articles & Resources
  • About LSTI
    • LSTI Leadership
    • LSTI Instructors
    • Contact Us
    • Connect with LSTI
    • Frequently Asked Questions
  • Connect

Clinical Trials & Good Clinical Practices (GCP) Training

  • $279
    It’s Ten O’Clock. Do You Know Where Your Trial Master File Is?
    Carmella Britt
    On-demand
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  • $279
    Project Management: Best Practices for Validation & Regulatory Projects
    Bruce Fieggen
    On-demand
    0
    0
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  • $799
    Clinical Regulatory Document Management Compliance Professional (CRDMCP)
    Daniel Orfe, Betsy Fallen
    On-demand
    0
    0
    $897.00 $799.00
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  • $279
    Building a Quality Risk Management Program and Leveraging Technology for Risk Based Monitoring
    Angie Maurer
    On-demand
    0
    0
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  • $279
    Regenerative Medicine: Understanding the Regulatory Landscape
    Kelly Lightfoot, Andrew Ittleman
    On-demand
    0
    0
    View more
  • $279
    Effective Clinical Investigator GCP Training – Getting It Right The First Time
    Sandra “SAM” Sather
    On-demand
    0
    0
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  • $279
    CRO Selection and Oversight – A Risk-Based Approach
    Sandra “SAM” Sather
    On-demand
    0
    0
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  • $279
    CRA Oversight – A Risk-based Approach
    Sandra “SAM” Sather
    On-demand
    0
    0
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  • $279
    A Risk-based Study Management Approach for Clinical Trial Sites
    Sandra “SAM” Sather
    On-demand
    0
    0
    View more
  • $279
    Understanding & Implementing The Revised NIH & FDA Clinical Trial Protocol Template
    Michael Pierro
    On-Demand
    0
    0
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  • $149
    Good Clinical Practices (GCP) Overview for Clinical Research Professionals – A Global Primer
    Michael Pierro
    On-demand
    0
    0
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  • $279
    Conducting the CRO Pre-qualification Audit for GCP Compliance – Key Risk Factors to Avoid
    Michael Pierro
    On-demand
    0
    0
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  • $279
    Clinical Study Requirements – Understanding Differences Between the US and EU
    Michael Pierro
    On-Demand
    0
    0
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  • $279
    Quality by Design (QbD) in Clinical Trials – Build Bullet-Proof Protocols
    Peter Schiemann
    On-demand
    0
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  • $279
    Strategic Clinical Project Management: Principles and Practical Applications
    Lydia Dyett
    On-demand
    0
    0
    View more
  • $279
    Partnership Strategies with CRO/Vendors: Create Relationships that Create Results
    Keri Urwin
    On-demand
    0
    0
    View more
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CATEGORIES

  • Coronavirus / COVID-19 (4)
  • Clinical Trials & Good Clinical Practices (GCP) Training (110)
  • Introductory Pharma Courses (18)
  • IT & Data Integrity for Pharma (33)
  • Leadership & Training (40)
  • Manufacturing & Good Manufacturing Practices (GMP) Training (92)
  • Medical Device Training (63)
  • On-Demand Courses (239)
  • Quality (52)
  • Regulatory & Compliance (208)
  • Research & Development (80)
  • Special Packages (5)

Upcoming Live Courses

  • China GCP 2020: Understanding and Implementing New Compliance Requirements
  • How to Prepare for FDA Guidance on Computer Software Assurance (CSA) in 2021 – A Two Part Primer
  • It is Finally Here! Update to the ISO Medical Device GCP Standard: ISO 14155:2020
  • Preparing for Changes to ICH GCP E6(R3) and ICH E8(R1) – Readying for Risk Mitigation

TOPICS

Cleaning Validation Cleanroom Clinical Trials Cloud CMOs Computer Systems CRAs CROs Data Integrity Device eCTD EHRs EMA Equipment Facilities FDA GCP GDP GLP GMP HIPAA Human Error ICH Informed Consent Inspections Instructional Design Management manufacturing Marketing MDR microbial control Process Validation Project Management QMS Quality Quality by Design Quality Risk Management Remote Monitoring Risk Risk-Based Monitoring Root Cause Analysis Site Monitoring SOPs Training Trial Master File

Your Courses

About Us

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 Us

  • 19 W College Ave. Ste 300, Yardley, PA 19067
  • +1-267-274-5133
  • info@lifesciencetraininginstitute.com

Course Categories

  • Clinical Trials & Good Clinical Practices (GCP) Training
  • Coronavirus / COVID-19
  • Introductory Pharma Courses
  • IT & Data Integrity for Pharma
  • Leadership & Training
  • Manufacturing & Good Manufacturing Practices (GMP) Training
  • Medical Device Training
  • On-Demand Courses
  • Quality
  • Regulatory & Compliance
  • Research & Development
  • Special Packages

Meet Our Instructors

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