Displaying 1–25 of 59 results for EtQ
New Training System Incorporates Testing, Learning Management Features
Four reasons why you should do it, and three reasons why youre not.
This white paper will provide an overview of the benefits and best practices of using the FDA's MedWatch Plus initiative for electronic adverse event reporting within the pharmaceutical industry, as well as other FDA-regulated organizations.
This white paper will look at how risk management provides the framework for handling adverse events in a systematic way—from design, to post-market events, to tracking and trending risk across the enterprise.
This white paper discusses the benefits of connecting the supply chain to your quality system, how to alleviate security concerns, and how to manage supplier performance.
the results and analysis of a recent industry survey indicating the need for an integrated, systematic approach to corrective and preventative action.
Couldnt make the trip to Chicago? The weather outside was frightful, but the technology was cutting edge. Pharmaceutical Manufacturings editors take a look at who and what was at this years conference.
New report analyzes survey results that point to an overall lack of confidence in current quality management systems
With the product lifecycle moving so fast, many organizations may ask the question, "How can we effectively measure quality?" What can an organization do to keep up with this new pace of business while ensuring the visibility that quality deserves? The answer is Risk Management.
Managing your Risk Has Its Rewards: Making the Case for Risk Assessment in Streamlining your Quality and Compliance Processes
Learn more about eMDR.