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Learn how partial proof testing of level instruments can save millions of dollars and maintain required safety ratings.
This infographic, based on a study by Peerless Research, illustrates the benefits supply chain, manufacturing and operations executives are experiencing across industry segments.
The pharmaceutical manufacturing landscape has changed notably over the past decade and is continuing to evolve rapidly. Pharmaceutical manufacturers have begun to wield some new tools, nailing down new efficiencies and better drugs in the process.
The following report reveals how highly integrated lab information technologies can power innovation and ensure that operational excellence is the rule, rather than the exception, in your organization’s lab operations.
In a study conducted by Peerless Research Group (PRG), 140 supply chain executives having management and/or purchase decision responsibilities for supply chain solutions in manufacturing and warehousing operations offered input on their current supply chain infrastructures.
The Best of Pharmaceutical Manufacturing eBook is a collection of the most-read feature articles from 2014, chosen by the Pharmaceutical Manufacturing digital audience.
This eBook includes articles addressing some newer thinking and approaches for manufacturing solid dose pharmaceutical products.
This eBook reveals how well-designed, well implemented information technologies can fulfill the lab’s critical mission.
This eBook, the first in a series from WellSpring Pharma Services, will provide you with the knowledge to effectively choose a contract manufacturing facility, and to understand common regulatory matters that influence the manufacturing and packaging of your product.
Whether you have a presence in Italy, or work with partners who do, download the new Pharmaceutical Theft In Italy alert to gain insight into the vulnerabilities, where they occur, causes, costs, and potential impact beyond Italy's borders.
Although the state of the pharmaceutical manufacturing union is strong, the continuing growth in the global demand for affordable prescription and over-the-counter drugs is challenging the industry in new ways to be able to manufacture enough safe, high quality drugs cost effectively and ...
This white paper outlines some of the elements that should be considered by a sponsor pharmaceutical company when outsourcing secondary processing (i.e. dosage form transfer, scale-up and commercial manufacture) of a highly potent product.
Both glass and plastic have their strengths and challenges, and many advancements have recently occurred within each “camp.”
This paper reviews an alternate method for rapid determination of the moisture levels in a closed sample vial -- portable NIR technology.
This report explains how a wall pass-through system that incorporates single-use components can reduce contamination risks and the use of valuable resources.
This case study demonstrates how a commercial manufacturing partnership between a pharmaceutical contract manufacturer and a large pharmaceutical company resulted in the establishment of a high volume process for Highly Potent Active Pharmaceutical Ingredients.
This case study provides an overview of the implementation of a framework that addressed both the usual technical challenges and also the business challenges in a recent real-world tech transfer involving the commercial manufacture of a solid oral dose product.
This white paper discusses the roles of sponsors and their contract manufacturing organization (CMO) partners regarding metrics, what metrics to measure, how to manage data, effective communications and ownership, and ways to improve metrics.
The chemical, pharmaceutical and food industries awaken to the explosive potential of dust accumulations in the plant. This eBook offers an overview of the dangers of dust accumulation in the plant and approaches for reducing this hazard.
Explore MasterControls’s quality, compliance and risk management solutions addressing these challenges.
To help guide strategic thinking, this eBook offers a deeper dive into the benefits of content management applications in the regulated cloud and strategies for 21 CFR part 11 compliance.
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.