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Life Science Training Institute
  • WEBINARS/eLEARNING
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    • On-Demand 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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  • Connect
  • 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

Research & Development

Speed-to-market is the goal for companies in pharmaceutical development.  Everyone is affected if you or your team lack efficient product development skills.

LSTI’s research and development courses cover all aspects of the development process. Our instructors provided real life case studies and sound clinical practices to help you get through regulatory review and approval.

Our trainers are industry subject matter experts (SMEs) who average over 20 years of life science and pharmaceutical experience.

Browse our research and development courses today.

  • $279
    How to Prepare for FDA Guidance on Computer Software Assurance (CSA) in 2021 – A Two Part Primer
    Kathleen Warner
    On-Demand
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  • $179
    It is Finally Here! Update to the ISO Medical Device GCP Standard: ISO 14155:2020
    Sandra “SAM” Sather
    On-Demand
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  • $179
    Preparing for Changes to ICH GCP E6(R3) and ICH E8(R1) – Readying for Risk Mitigation
    Sandra “SAM” Sather
    On-Demand
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  • $279
    Quality Management of Electronic Systems in Clinical Trial Investigations: A Comparison of FDA and EMA Guidance
    Sandra “SAM” Sather
    On-Demand
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  • $279
    Regulatory Affairs in China – The New Drug Regulatory Framework
    Michael Zhang, Katrin Rupalla
    On-Demand
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  • $179
    Pharmaceutical Sampling Plans – Understanding for Compliance
    Mark Allen Durivage
    On-Demand
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  • $179
    Critical Documentation of Clinical Trial Activities and CAPA During and Post COVID-19 Restrictions
    Sandra “SAM” Sather
    On-Demand
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  • $179
    Conducting a Virtual GCP Audit of a CRO Managed Study During the COVID-19 Pandemic
    Michael Pierro
    On-Demand
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  • $179
    Remote Auditing for GMP Compliance During COVID-19: Challenges and Opportunities
    Mark Allen Durivage
    On-Demand
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  • $179
    Remote Monitoring Operations While Maintaining HIPAA and GCP During COVID-19 Restrictions
    Sandra “SAM” Sather
    On-Demand
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  • $279
    Drug Substance Quality Risk Management: A Practical Approach to Identify Critical Quality Attributes and Critical Process Parameters
    Kevin Wall
    On-Demand
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  • $279
    Clinical Research Project Management – 7 Breakthrough Behaviors For Success
    Dalfoni Banerjee
    On-Demand
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  • $279
    Applying Six Sigma Tools and Concepts in Clinical Research: A Process Improvement Guide
    Betsy Fallen
    On-Demand
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  • $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
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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.

EMAIL COMMUNICATIONS

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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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