Manufacturing & Good Manufacturing Practices (GMP) Training
LSTI’s good manufacturing practices (GMP) webinars and on-demand courses provide pharmaceutical and life science professionals with actionable, practical GMP best practices.
GMP ensures your company can consistently produce and control your products according to quality standards. Our interactive webinars help you and your team increase your GMP expertise. On-demand courses enable you to receive just-in-time training that best suits your schedule.
Our trainers are industry subject matter experts (SMEs) who average over 20 years of life science and pharmaceutical experience.
Browse our GMP training courses below.
Showing 1–16 of 92 results
-
How to Prepare for FDA Guidance on Computer Software Assurance (CSA) in 2021 – A Two Part Primer
$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 -
Remote Auditing for GMP Compliance During COVID-19: Challenges and Opportunities
$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 -
Essentials of Disinfectant Efficacy Testing: Ensuring Microbial Control
$279.00 – $2,550.00 Read more -
Implementing a Robust Change Control Program – Key Elements for Process and Documentation Compliance
$279.00 – $2,550.00 Select options -
Blockchain Technology for the Life Sciences: A Comprehensive Primer
$279.00 – $2,550.00 Read more -
How FDA and MHRA Decide Which Drug Facilities to Inspect – and at What Frequency
$279.00 – $2,550.00 Select options -
Aseptic Process Validation: Top-Tips for Compliance and Success
$279.00 – $2,550.00 Select options -
A Holistic Approach to External GMP Surveillance, GMP Training, and Quality Knowledge Management
$279.00 – $2,550.00 Select options -
Elemental Impurities Tests for Pharmaceutical Products According to the New ICH Q3D and USP 232/233 Guidelines
$279.00 – $2,550.00 Select options -
Writing Effective 483 and Warning Letter Responses
$279.00 – $2,550.00 Read more -
Establishing Appropriate Quality Metrics
$279.00 – $2,550.00 Read more -
FDA Compliant QC and QA Practices: Creating a Perfect, Audit-Ready QMS
$279.00 – $2,550.00 Select options -
Executing Proper Event Investigations: Critical Steps In Ensuring Compliant Corrective Actions
$279.00 – $2,550.00 Select options