On-Demand Courses
On-demand courses for a demanding industry– we know you’re busy and LSTI has a solution for you to get the training you need, when you need it.
Our pharmaceutical and life sciences training courses are ready when you are. When you sign up for one of our prerecorded live sessions, you’ll get the same live content, but delivered at your convenience.
Whether it’s GxP, manufacturing, research, or medical devices, there is a course that’s right for you.
Our trainers are industry subject matter experts (SMEs) who average over 20 years of life science and pharmaceutical experience.
Showing 1–16 of 239 results
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China GCP 2020: Understanding and Implementing New Compliance Requirements
$279.00 – $2,550.00 Select options -
How to Prepare for FDA Guidance on Computer Software Assurance (CSA) in 2021 – A Two Part Primer
$279.00 – $2,550.00 Select options -
It is Finally Here! Update to the ISO Medical Device GCP Standard: ISO 14155:2020
$179.00 – $1,695.00 Select options -
Preparing for Changes to ICH GCP E6(R3) and ICH E8(R1) – Readying for Risk Mitigation
$179.00 – $1,695.00 Select options -
Quality Management of Electronic Systems in Clinical Trial Investigations: A Comparison of FDA and EMA Guidance
$279.00 – $2,550.00 Select options -
Regulatory Affairs in China – The New Drug Regulatory Framework
$279.00 – $2,550.00 Select options -
Effective Writing for Investigation Authors and Reviewers
$279.00 – $2,550.00 Select options -
Pharmaceutical Sampling Plans – Understanding for Compliance
$179.00 – $1,695.00 Select options -
Critical Documentation of Clinical Trial Activities and CAPA During and Post COVID-19 Restrictions
$179.00 – $1,695.00 Select options -
Conducting a Virtual GCP Audit of a CRO Managed Study During the COVID-19 Pandemic
$179.00 – $1,695.00 Select options -
Remote Auditing for GMP Compliance During COVID-19: Challenges and Opportunities
$179.00 – $1,695.00 Select options -
Remote Monitoring Operations While Maintaining HIPAA and GCP During COVID-19 Restrictions
$179.00 – $1,695.00 Select options -
Drug Substance Quality Risk Management: A Practical Approach to Identify Critical Quality Attributes and Critical Process Parameters
$279.00 – $2,550.00 Select options -
FDA REMS Inspection Guide: Audit Preparedness Best Practices
$279.00 – $2,550.00 Select options -
Clinical Research Project Management – 7 Breakthrough Behaviors For Success
$279.00 – $2,550.00 Select options -
Identifying Workforce Gaps Post Risk-Based Monitoring (RBM): It’s Time to “DIG” in!
$279.00 – $2,550.00 Select options