Displaying 1–7 of 7 results for EtQ

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Research Report: Exploring Pharma's CAPA Challenges

(Whitepaper)

the results and analysis of a recent industry survey indicating the need for an integrated, systematic approach to corrective and preventative action.

How to Incorporate Suppliers into Your Quality and Compliance System While ...

(Whitepaper)

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.

Keeping up with the New Pace of Business: How Risk Management Tools Can ...

(Whitepaper)

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.

Enhancing Collaboration with the FDA Through eMDR

(Whitepaper)

Learn more about eMDR.

Managing your Risk Has Its Rewards: Making the Case for Risk Assessment in ...

(Whitepaper)

Managing your Risk Has Its Rewards: Making the Case for Risk Assessment in Streamlining your Quality and Compliance Processes

How Risk Management Tools Can Improve Product Quality in Today's Rapid ...

(Whitepaper)

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.

Enhancing Collaboration with the FDA Through MedWatch Plus

(Whitepaper)

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.

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