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  • Courses
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  • Blog & Resources
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Regulatory & Compliance

  • $279
    inspection
    Aseptic Process Simulations – A Comprehensive Guide for Proper Execution
    Danielle DeLucy
    On-Demand
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  • $279
    Authoring and Implementing Standard Operating Procedures (SOPs): Best Practices for Success
    Joanna Gallant
    On-Demand
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  • $279
    How FDA and MHRA Decide Which Drug Facilities to Inspect – and at What Frequency
    Jerry Chapman
    On-Demand
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  • $279
    Aseptic Process Validation: Top-Tips for Compliance and Success
    Kelly Thomas
    On-Demand
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  • $279
    Biocontainment For Manufacturing: Understanding The Risks, Guidance, and Design Requirements
    Erich Bozenhardt, Herman Bozenhardt
    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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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 Quality Quality by Design Quality Risk Management Remote Monitoring Risk Risk-Based Monitoring Root Cause Analysis Site Monitoring SOPs Training Trial Master File Upcoming Courses

Your Courses

Upcoming Live Courses

  • Clinical Research Project Management - 7 Breakthrough Behaviors For Success
  • Essentials of Disinfectant Efficacy Testing – Ensuring Microbial Control
  • The MHRA Data Integrity Guidance Clarified: What it Means for Industry & Patients
  • Implementing a Robust Change Control Program – Key Elements for Process and Documentation Compliance
  • Responding to Clinical Observations: Developing Robust Audit & Inspection CAPAs
  • CAPA and Root Cause Analysis: Essentials Post ICH GCP E6 (R2) Addendum
  • Medical Device Recalls – Keys To Implementing A Successful Approach

Contact

  • 101 Gibraltar Road, Suite 100. Horsham, PA 19044
  • 215-675-1800 (option 3)
  • info@lifesciencetraininginstitute.com
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