WEBINARS - HRPF

Writing SOP’s and Work Instructions that Really Work

Clinical Trial Master File (TMF) and Electronic Trial Master File (eTMF)

Avoid Warning Letters in View of the U.S. FDA's Stated Goal

Effective Design of Experiments (DOE) Strategies

Risk Management and Impact Assessments in Change Control

Statistical Process Control (SPC) and Control Charts for Laboratory Compliance

Statistical Process Control (SPC) and Control Charts - In Accordance with Latest FDA Expectations

Data Integrity – In compliance with CSA, 21 CFR Part 11, SaaS/Cloud and EU GDPR

The Supervisor's Guide to a Human Error-Free Environment

Practical Implementation of Pharmaceutical Quality Risk Management (QRM)

3-Hour Virtual Seminar on Bad Standard Operating Procedures (SOPs) – Bad Training: Garbage In, Garbage Out

Developing Effective Post Market Surveillance and Complaint Handling Requirements (Interrelationship with CAPA, Change Control, Adverse Event Reporting and Recalls)

This article discusses the significance of developing effective post-market surveillance and complaint handling requirements and their interrelationship with CAPA, change control, adverse event reporting, and recalls.