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Life Science Training Institute
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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
    Writing Clinical Monitoring Reports: Using the Liquid Report Writing Method
    Sandra “SAM” Sather
    On-demand
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  • $279
    Source Data Review (SDR) vs. Source Data Verification (SDV) – A Site Monitoring Best Practices Update
    Sandra “SAM” Sather
    On-demand
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  • $279
    Root Cause Analysis for Clinical Research Professionals
    Sandra “SAM” Sather
    On-demand
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  • $279
    Risk-Based Monitoring Plan Development
    Sandra “SAM” Sather
    On-demand
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  • $279
    Remote Monitoring of Clinical Source Data – Why Not?
    Sandra “SAM” Sather
    On-demand
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  • $279
    Remote Monitoring Implementation Post ICH GCP E6 (R2): A Practical Guide
    Sandra “SAM” Sather
    On-demand
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  • $279
    The Power of Influencing – Achieving Patient-focused Outcomes to Guarantee Success
    Jill Donahue
    On-demand
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  • $279
    Building Accountability on Your Clinical Teams
    Janelle Brittain
    On-demand
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  • $279
    Identifying and Closing the Training Gap in Clinical Research
    Laurie Halloran
    On-demand
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  • $1649
    Course Vouchers – 10 Pack
     
    Voucher Package
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    0
    $1,649.00
    View more
  • $949
    Course Voucher – 5 Pack
     
    Voucher Package
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    0
    $1,495.00 $949.00
    View more
  • $279
    Authoring and Implementing Standard Operating Procedures (SOPs): Best Practices for Success
    Joanna Gallant
    On-Demand
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  • $279
    Monitoring Medical Device / ISO 14155 GCP
    Sandra “SAM” Sather
    On-Demand
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  • $279
    Document Authoring, Archive, and Inspection – Challenges And Tips For Establishing Audit-Proof Processes
    Daniel Orfe, Betsy Fallen
    On-demand
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  • $279
    Change Management Plan Development for Risk-Based Clinical Studies: From Site Monitoring to Vendor Management and Beyond
    Angie Maurer
    On-Demand
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  • $279
    Understanding The New NIH/HHS Final Rule On Clinical Trial Reporting – Tips For Compliance Success
    Michael Pierro
    On-demand
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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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