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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
    Essentials of Disinfectant Efficacy Testing: Ensuring Microbial Control
    Crystal Booth
    On-Demand
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  • $279
    Clinical Quality Management Systems (QMS): Establishing a Practical & Compliant Program
    Penelope Przekop, MSQA, RQAP-GCP
    On-Demand
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  • $279
    The MHRA Data Integrity Guidance Clarified: What it Means for Industry & Patients
    Betsy Fallen
    On-Demand
    2
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  • $279
    Blockchain Technology for the Life Sciences: A Comprehensive Primer
    Brooke L. Casselberry
    On-Demand
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  • $279
    Developing a Part 11 Compliance Plan in Clinical Research
    Lisa Olson
    On-Demand
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  • $279
    Establishing Appropriate Quality Metrics
    Kelly Thomas
    On-Demand
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  • $279
    Responding to Clinical Observations: Developing Robust Audit & Inspection CAPAs
    Penelope Przekop, MSQA, RQAP-GCP
    On-Demand
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  • $279
    Measuring CAPA Effectiveness: Critical Tips in Getting the Right CAPA and Showing It Works
    Joanna Gallant
    On-Demand
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  • $279
    Note to File 101: Critical Steps for When, and When Not To, Engage in NTFs
    Luisa Monica, Jackie Morrill
    On-Demand
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  • $279
    Right to Try Legislation: Impact on Industry, Health Authorities, and Patients
    Michael Pierro
    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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  • $199
    The Value of the Medical Affairs Organization: A Comprehensive Overview
    Judith Serafin
    On-Demand
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  • $279
    Mock Regulatory Inspections: How to Get the Best Bang for Your Buck
    Penelope Przekop, MSQA, RQAP-GCP
    On-Demand
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  • $279
    Use of Electronic Records and Electronic Signatures in Clinical Investigations Under 21 CFR Part 11
    Sandra “SAM” Sather
    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
    Electronic Document Management Systems (EDMS) & Electronic Common Technical Documents (eCTD): An Overview
    Daniel Orfe, Betsy Fallen
    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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