Regulatory & Compliance
Are you confident that your work aligns with the most current regulatory compliance requirements? Failure is an expensive lesson that shouldn’t be taken lightly. You can prevent FDA warning letters if you and your team are current on GxP best practices.
Our interactive webinars help you and your team increase your compliance skill and regulatory knowledge– enabling you to ask real life questions to our training experts. 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 regulatory and compliance training courses below.
Showing 1–16 of 208 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 -
Identifying Workforce Gaps Post Risk-Based Monitoring (RBM): It’s Time to “DIG” in!
$279.00 – $2,550.00 Select options -
Applying Six Sigma Tools and Concepts in Clinical Research: A Process Improvement Guide
$279.00 – $2,550.00 Read more -
New FDA Draft Guidance: A Risk-Based Approach to Monitoring Clinical Investigations
$279.00 – $2,550.00 Select options