Displaying 1–25 of 34 results for MasterControl
MasterControl Inc. on Jan. 23 released MasterControl Version 6, which vastly expands the companys offerings with the introduction of five new modules.
MasterControl Rules Software monitors quality events for FDA-regulated and ISO-certified companies.
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.
Adopting Enterprise Quality Management Software is an imperative Pharma companies can’t ignore
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
How innovative EBR solutions are making it easier to scrap paper-based processes
A growing number of quality management and compliance packages can help you seize control of processes and documentation, and prepare for FDA audits.
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 ...
Explore MasterControls’s quality, compliance and risk management solutions addressing these challenges.
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...
By implementing supplier audits collaboratively and applying robust quality management tools, manufacturers are much more likely to achieve supplier quality success
By integrating data systems and processes, companies can reduce errors and human touch all the way through a product’s lifecycle
Would zombies be more successful at world domination if they used an electronic quality management system?
Manhattan in the spring, a bustling show floor and thought-provoking educational sessions provide all the reason anyone should need to attend this years event
Pharmaceutical processing & engineering: In step with FDAs 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 ...
PhMs virtual panel weighs in on information technology trends in pharmaceutical manufacturing
Using the data deluge for better decision-making on the plant floor
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
The Pharmaceutical Industry's Transition to Electronic Processes
How Effective Document Management Helps Pharmaceutical Companies Accelerate Time to Market
Six Corporate Oversights of Quality and Compliance Issues in Pharmaceutical Environments
How can we leverage our existing ERP if we adopt an electronic QMS? What are the things we should lo