Displaying 1–25 of 66 results for IT Management
the results and analysis of a recent industry survey indicating the need for an integrated, systematic approach to corrective and preventative action.
When it comes to the biologics product development lifecycle, information management is an imperative that cannot be ignored.
It would be foolish to underestimate the risk associated with aseptic drug processing. Drug safety, secure uninterrupted supply, as well as regulatory imperatives dictate that drug makers create intensive and verifiable systems to assure sterility in aseptic processing environments.
This eBook reveals how well-designed, well implemented information technologies can fulfill the lab’s critical mission.
Explore MasterControls’s quality, compliance and risk management solutions addressing these challenges.
This white paper contains expert insights on how to much more effectively manage Environment Monitoring in manners that increase efficiency, increase compliance and decrease risk.
This white paper, first in a series of three, is to help executives and managers assigned to provide due-diligence of prospective contract manufacturing partners a framework in which to make a solid, objective evaluation of its overall operational excellence as it relates to quality.
Why Companies Need Best-of-Breed ERP and EQMS and how PLM fits into the mix
The FDA mandates the validation of environmental conditions that can affect the strength, identity, safety, quality, and purity of pharmaceuticals, medical devices, or biologics.
To meet important regulatory challenges, it is imperative that manufacturers have a quality management system to manage processes and provide timely access to relevant data, effectively and efficiently.
The Best of Pharmaceutical Manufacturing 2013 eBook provides a comprehensive overview of the key challenges faced by manufacturers within the complex pharmaceutical industry landscape.
Learn how companies can move on from solubility when it comes to cleaning validation.
This App Note explains how to ensure continued GxP compliance in your monitoring system for temperature-controlled environments.
How to Execute a System Integration Project
As drug manufacturers strive to retain highly skilled labor, increasing employee compensation is not always an option, or the answer. A more feasible strategy focuses on increasing employee engagement. This paper explains why and how an automated workforce management approach can make it possible.
This research report from the Aberdeen Group offers insight into the manufacturing sector. Automation is critical to achieve the level of visibility, productivity, and profitability that manufacturers require. Not only does automation support efficient and effective processes, but it also enables...
Since FDA introduced the term to the pharmaceutical industry in 2005, the concept of pharmaceutical quality by design (pharma QbD), a framework for building quality into pharmaceuticals during drug development has been slowly gaining ground. Discrete industries are no strangers to QbD. Now, ...
Experts often repeat the fact that no single analytical technology should dominate any pharmaceutical quality control toolkit.
Raman spectroscopy is establishing a major presence in pharma QC applications, especially as portable, miniaturized systems have entered the marketplace.
As drug manufacturers strive to retain highly skilled labor, increasing employee compensation is not always an option, nor the best answer. A more feasible strategy focuses on increasing employee engagement. This paper explains why and how an automated workforce management approach can make it ...
Why can't drug manufacturers manage their workforces as well as they do machines and materials? This special 11-page PDF, with clickable links to additional web resources, provides articles and insight into pharma's struggle to incorporate Lean into its operations, and about how applying Lean ...