Displaying 1–7 of 7 results for MasterControl

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Solutions Update: Quality, Compliance, Regulatory and Risk Management ...

(Whitepaper)

Explore MasterControls’s quality, compliance and risk management solutions addressing these challenges.

The Pharmaceutical Industry's Transition to Electronic Processes

(Whitepaper)

The Pharmaceutical Industry's Transition to Electronic Processes

How Effective Document Management Helps Pharmaceutical Companies Accelerate ...

(Whitepaper)

How Effective Document Management Helps Pharmaceutical Companies Accelerate Time to Market

Six Corporate Oversights of Quality and Compliance Issues in Pharmaceutical ...

(Whitepaper)

Six Corporate Oversights of Quality and Compliance Issues in Pharmaceutical Environments

How Effective Document Management Helps Accelerate Time to Market

(Whitepaper)

In the drug development process, time is indeed money. On the one hand, it takes a decade or longer to develop a new medicine. On the other hand, the patent for a new drug typically lasts 20 years. That leaves a manufacturer only a few years of market exclusivity before its patent expires and ...

5 Ways to Ensure System Compliance with 21 CFR Part 11

(Whitepaper)

The FDA is currently re-examining the interpretation scope of 21 CFR Part 11, the landmark regulation that made electronic records and signatures as valid as hard-copy equivalents. In this paper, MasterControl offers five tips to ensure your quality system is Part 11-compliant and strengthen your...

Tracking Training in FDA Environments

(Whitepaper)

Well-managed training programs minimize the risk of noncompliance and enhance product quality. Brian Curran, senior VP of product management and strategic marketing for MasterControl Inc., gives an in-depth look at how drug manufacturers can monitor and optimize employee training.

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