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GlobalCompliancePanel Press releases

11 - 20 of 219 Press Releases

May 09, 2013
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.

Apr 29, 2013
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.

Apr 08, 2013
The ICH Q-10 guidelines, which have been in force since 2006, have specific instructions for application of drug...

Apr 05, 2013
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...

Apr 04, 2013
RAPS pre-approved webinar on “Statistics for Quality Control and Process Validation: Statistical Process Control (SPC) for Variable Data” from...

Mar 25, 2013
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 &...

Mar 22, 2013
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.

Mar 21, 2013
Description: This course is about the Hazard Analysis and Critical Control Point (HACCP). It will introduce the role of the HACCP.

Mar 13, 2013
Description: Employee turnover is one of the major problems that plague the clinical research industry.

Mar 12, 2013
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”.

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