All Courses
The Life Science Training Institute (LSTI) helps pharmaceutical, biotech, and medical device companies build knowledgeable, compliant workforces by providing training on topics ranging from drug discovery to commercialization.
We are passionate about advancing careers of those working to develop new therapies and to protect patient safety.
Our courses are taught by seasoned subject matter experts (SMEs) who average over 20 years of clinical trial experience.
Browse our training courses below or select a topic to refine your search.
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How to Prepare for FDA Guidance on Computer Software Assurance (CSA) in 2021 – A Two Part PrimerKathleen WarnerOn-Demand00
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It is Finally Here! Update to the ISO Medical Device GCP Standard: ISO 14155:2020Sandra “SAM” SatherOn-Demand00
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Preparing for Changes to ICH GCP E6(R3) and ICH E8(R1) – Readying for Risk MitigationSandra “SAM” SatherOn-Demand00
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Quality Management of Electronic Systems in Clinical Trial Investigations: A Comparison of FDA and EMA GuidanceSandra “SAM” SatherOn-Demand00
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Regulatory Affairs in China – The New Drug Regulatory FrameworkMichael Zhang, Katrin RupallaOn-Demand00
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Critical Documentation of Clinical Trial Activities and CAPA During and Post COVID-19 RestrictionsSandra “SAM” SatherOn-Demand00
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Conducting a Virtual GCP Audit of a CRO Managed Study During the COVID-19 PandemicMichael PierroOn-Demand00
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Remote Auditing for GMP Compliance During COVID-19: Challenges and OpportunitiesMark Allen DurivageOn-Demand00
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Remote Monitoring Operations While Maintaining HIPAA and GCP During COVID-19 RestrictionsSandra “SAM” SatherOn-Demand00
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FDA REMS Inspection Guide: Audit Preparedness Best PracticesPenelope Przekop, MSQA, RQAP-GCPOn-Demand00
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Clinical Research Project Management – 7 Breakthrough Behaviors For SuccessDalfoni BanerjeeOn-Demand00
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Identifying Workforce Gaps Post Risk-Based Monitoring (RBM): It’s Time to “DIG” in!Sandra “SAM” SatherOn-Demand00