GlobalCompliancePanel

Computer systems need to be compliant in relation to a few important areas. Some areas of regulation relating to implementation of computerized systems can be worked out for better results.

This course will present the procedures that must be used in the application of DOE and SPC to the development, design and monitoring of manufacturing and testing processes.

The ICH Q-10 guidelines, which have been in force since 2006, have specific instructions for application of drug...

GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, “New EU Pharmacovigilance Directive and Regulations” on April...

RAPS pre-approved webinar on “Statistics for Quality Control and Process Validation: Statistical Process Control (SPC) for Variable Data” from...

GlobalCompliancePanel to hold two-day, in-person seminar in Philadelphia on the topic, “Software Validation for the New FDA Inspections” on April 18 and 19, 2013( Thursday &...

Description: This webinar is about regulations found in FDA QSR manual and how they need to be implemented.   FDA's Quality system Regulation (QSR) sets requirements for acceptance activities related to medical device manufacture.

Description: This course is about the Hazard Analysis and Critical Control Point (HACCP). It will introduce the role of the HACCP.

Description: Employee turnover is one of the major problems that plague the clinical research industry.

Description:This webinar discusses the criticality of Good Documentation Processes (GDP) in the pharmaceutical industry. The FDA is clear and unambiguous in its declaration: “If it isn’t written down, it didn’t happen”.