Displaying 1–25 of 34 results for MasterControl

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MasterControl Inc.

(Product)

MasterControl Inc. on Jan. 23 released MasterControl Version 6, which vastly expands the company’s offerings with the introduction of five new modules.

MasterControl Inc.

(Product)

MasterControl Rules Software monitors quality events for FDA-regulated and ISO-certified companies.

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.

Don’t Slow Your EQMS Adoption Roll

(Article)

Adopting Enterprise Quality Management Software is an imperative Pharma companies can’t ignore

5 Tips for Conducting a Supplier Audit

(Article)

To ensure that a supplier can provide the material or products meeting quality specifications and requirements, consider these five things when conducting an onsite supplier audit

Curing Batch Record Pain Points

(Article)

How innovative EBR solutions are making it easier to scrap paper-based processes

A Compliance and Traceability Toolkit

(Article)

A growing number of quality management and compliance packages can help you seize control of processes and documentation, and prepare for FDA audits.

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 ...

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

(Whitepaper)

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

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...

Supplier Audits -- Do's and Don'ts: Managing Supplier Quality & Reliability

(Article)

By implementing supplier audits collaboratively and applying robust quality management tools, manufacturers are much more likely to achieve supplier quality success

Save Money, Make Money: IT Integration and Data Exchange

(Article)

By integrating data systems and processes, companies can reduce errors and human touch all the way through a product’s lifecycle

Why Zombies Would Be Unstoppable if They Used a QMS

(Article)

Would zombies be more successful at world domination if they used an electronic quality management system?

What to Expect at Interphex 2007

(Article)

Manhattan in the spring, a bustling show floor and thought-provoking educational sessions provide all the reason anyone should need to attend this year’s event

Redefining the Workforce

(Article)

Pharmaceutical processing & engineering: In step with FDA’s 21st Century GMPs, more drug manufacturers are working to better understand and control their processes. Biotechnology, and concepts such as process analytical technology (PAT), continuous processing and more advanced control promise to ...

What’s Trending in IT

(Article)

PhM’s virtual panel weighs in on information technology trends in pharmaceutical manufacturing

Product Focus: Making the Most of Data

(Article)

Using the data deluge for better decision-making on the plant floor

Therapeutic Dose: 'Til Death do us Part... But First, Here's the Pre-Nuptial ...

(Article)

The CAPA is still necessary, but it needs to morph into something new under the QbD and PAT manufacturing examples, argues Contributing Editor Emil Ciurczak.

Tech Talk: Business Management Solutions

(Article)

Tech Talk: Business Management Solutions

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

Master Control Inc.

(Product)

PathWise and Document Control Systems

(Product)

Information Technologies, Data Management, Informatics Expert Forum: Adopting...

(Ask The Experts)

How can we leverage our existing ERP if we adopt an electronic QMS? What are the things we should lo

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