Displaying 1–22 of 22 results for EtQ
the results and analysis of a recent industry survey indicating the need for an integrated, systematic approach to corrective and preventative action.
New report analyzes survey results that point to an overall lack of confidence in current quality management systems
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.
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.
Learn more about eMDR.
Managing your Risk Has Its Rewards: Making the Case for Risk Assessment in Streamlining your Quality and Compliance Processes
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.
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.
New Training System Incorporates Testing, Learning Management Features
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.
On-demand, concise tutorials on the fundamental concepts of pharmaceutical manufacturing, process development, quality control and compliance brought to you by Pharmaceutical Manufacturing.
A free library of downloadable pharmaceutical industry white papers