Displaying 1–25 of 36 results for Unit Operations

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Research Report: Filling Pharma’s Label Management Void

(Whitepaper)

Industry survey indicates pharma’s need to move towards a single, connected label management solution.

eBook: Facilities and Operational Investment

(Whitepaper)

Pharma’s operational excellence is being fueled by increased capital spending.

eBook: State of Pharmaceutical Manufacturing 2015

(Whitepaper)

If behavior often speaks volumes, then the pharmaceutical industry is saying a lot lately in the way that it is responding to the social and economic forces that affect its markets and the potential commercial success of the drugs they develop and deliver around the world.

eBook: Solid Dose Spotlight

(Whitepaper)

Seeking Agile, Excellent Oral Solid Dose Operations

eBook: Pharmaceutical Equipment & Manufacturing Trends

(Whitepaper)

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.

eBook: Advancing Solid Dose Manufacturing

(Whitepaper)

This eBook includes articles addressing some newer thinking and approaches for manufacturing solid dose pharmaceutical products.

eBook: State of Pharmaceutical Manufacturing 2014

(Whitepaper)

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 ...

Learn about Mitigating Risk, Maximizing Compliance in Outsourcing Relationships

(Whitepaper)

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.

The Pharmaceutical Industry's Transition to Electronic Processes

(Whitepaper)

The Pharmaceutical Industry's Transition to Electronic Processes

Calculating Total Uncertainty of Temperature Calibration with a Dry Block

(Whitepaper)

This article will discuss the various uncertainty components related to temperature calibration using a temperature dry-block. Also, it will discuss how to calculate the total uncertainty of a calibration performed with a dry block.

Biopharmaceutical Process Scale Up: Get It Right

(Whitepaper)

Scaling up any biopharmaceutical process requires a clear understanding of both "real world" and laboratory conditions. Success ultimately depends on close process monitoring, and sensitive and accurate sensors.

Examining the Role of TOC Analyzers in the Pharmaceutical Laboratory

(Whitepaper)

Total Organic Carbon (TOC) analyzers serve a vital role in the pharmaceutical lab, in both the drug development and manufacturing processes. Presented here is an overview, as well as application examples showcasing TOC for Cleaning Validation and to address such guidelines as USP <643>.

The Safest Way to Calibrate: An Introduction to Intrinsically Safe Calibration

(Whitepaper)

Intrinsically safe calibrators are not only the safest possible calibration equipment—used even for Zone 0 environments—but also provide the functionality and performance of regular industrial calibration devices. This paper provides a primer on the meaning and benefits of intrinsically safe ...

Turning Data Into Information: Making Sense of an Avalanche of Supply Chain ...

(Whitepaper)

Biomanufacturing and operations research experts describe how to deal with staggering volumes of production and supply chain data. Learn how to convert this data into actionable information, which will be of value to the whole organization. Read about consolidating data from disparate sources, ...

Zeta Plus Activated Carbon Cartridges Evaluation & Scale-Up for ...

(Whitepaper)

This Technical Brief describes how the Zeta Plus Activated Carbon Cartridge series is evaluated for use in pharmaceutical applications and how the optimal carbon type and media grade are chosen for a given application. In addition, the brief describes how a process is scaled-up in order to ...

Increasing Tablet Press Productivity Using Segmented Turret Technology

(Whitepaper)

Surveys of tablet press users reveal that machines with segmented turrets increase output and reduce set-up and cleaning time over conventional presses and previous turret technologies. This paper will discuss survey data from drug manufacturers using the technology and quantify some of the ...

Complying With U.S. FDA Title 21 CFR Part 11 for the Life Sciences Industry

(Whitepaper)

The purpose of this document is to describe the functions and features of SAP ERP that demonstrate technical compliance with U.S. FDA 21 CFR Part 11 Electronic Records; Electronic Signatures Final Rule and several international good manufacturing practice (GMP) guidelines having similar ...

Using a Coriolis Flowmeter's Multivariable Characteristics to Validate ...

(Whitepaper)

The most common maintenance operation for any flow metering technology is focused around validating the device's calibrations stability over time. This document describes a procedure that uses the multivariable capabilities of a Micro Motion Coriolis flowmeter to provide an in-situ validation of ...

Reduce Contamination Risk with Advanced Local User Notification Indicators ...

(Whitepaper)

During continuous particle monitoring of a cleanroom environment, a meaningful user notification system near the point of sampling is an important factor in successful intervention and root cause analysis of particle events. Though many remote optical air particle counter suppliers feature a ...

Single, Straight-Tube Coriolis Sensors: Installation Best Practices for ...

(Whitepaper)

Biopharmaceutical manufacturing is performed in a highly sterile environment. Bioreactions take place over an extended period of time. For example, it can take 6-8 weeks to complete a single bioreactor batch. Given the time that is committed to manufacturing biopharmaceuticals and their market ...

AstraZeneca Decided for Paperless Solution

(Whitepaper)

AstraZeneca opted for a paperless solution that would allow for data trending and a centralized, accessible calibration data base. It is cost effective.

Assessment of Risk Factors in Container-Closure Systems

(Whitepaper)

This paper looks at applying Process Analytical Technologies to the lyophilization process to mitigate risk factors that could lead to producing a poor product. Dr. Jennings argues that risk can be lowered by increasing the number of samples, thereby raising the confidence level and reducing the ...

Process Modeling and Control Challenges in the Pharmaceutical Industry

(Whitepaper)

In this 2003 presentation made at a conference held by the University of Texas, Phil Dell'Orco, GSK's Leader for Process Safety and Design, summarized the challenges facing engineers as they work to improve control of pharmaceutical processes in an industry still dominated by chemists.

NIR and Imaging: Basic Principles and Pharmaceutical Applications

(Whitepaper)

This article by Gabriele Reich at the University of Heidelberg's Institute for Pharmaceutical and Molecular Biology examines the basics of NIR spectroscopy.

Phase Transformation in Solid Pharmaceutical Materials

(Whitepaper)

This 72-page PDF, a dissertation by Denny Mahlin at Sweden's Uppsala Faculty of Pharmacy, discusses results of using atomic force microscopy and other techniques to study solid mixtures for solid dosage forms.

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