Displaying 1–25 of 34 results for Aseptic Processing

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eBook: Aseptic Processing Trends

(Whitepaper)

Special Report: The Time is Right for Virtualization

(Whitepaper)

In this special report, we explore how virtualization can provide significant advantages for deploying process control systems at pharmaceutical plants.

Special Report: Addressing Process Contamination Risks

(Whitepaper)

The high risk involved with biopharmaceuticals means there are high demands placed on the hygienic design of bioprocessing equipment. Instrument connections on equipment are a known challenge in preventing process contamination, especially when they aren’t properly installed or maintained.

Pharma Packaging Trends 2016 eBook

(Whitepaper)

Once viewed as a mundane part of the business, primary packaging of pharmaceuticals has morphed into a hotbed of creativity.

2016 Liquid Dose Trends

(Whitepaper)

Parenteral drugs are taking a strong position alongside the more established oral solid dose forms and are quickly coming into their own

Pharmaceutical Packaging Trends eBook

(Whitepaper)

Pharmaceutical packaging plays a critical role in ensuring the efficient distribution and safe consumption of the world’s drug supply.

eBook: Advances in Aseptic Processing: Keeping Risk and Contamination at Bay

(Whitepaper)

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.

eBook: Glass vs. Plastic Pharmaceutical Packaging Trends

(Whitepaper)

Both glass and plastic have their strengths and challenges, and many advancements have recently occurred within each “camp.”

Aseptic Manufacturing: A Roadmap to Excellence

(Whitepaper)

Aseptic Manufacturing: A Roadmap to Excellence

Rotary Tank Cleaning and Cost Savings

(Whitepaper)

Specific case studies on the benefits of rotary impingement and CIP optimization vs. the standard tank cleaning processes. Benefits include: increased revenue and production with drastic reductions of operating costs pertaining to tank cleaning.

Best Practices from Baxter BioPharma: Optimizing Lyophilization and the ...

(Whitepaper)

Using empirical, or science-based, freeze-drying approaches versus trial and error can help you navigate potential commercialization roadblocks.

Cartridge Filtration in the Production of Pharma Grade Water

(Whitepaper)

This detailed paper from 3M illustrates its effective use for some of the most critical applications: the removal of particulates that might contaminate water systems, eliminating Pseudomonades and other microorganisms, reducing endotoxins, and protection of storage tanks during draw-down.

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 ...

Six Key Predictors of Outsourcing Success In A Maturing RE & FM Outsourcing ...

(Whitepaper)

In this white paper, Nicole Ballard and Rakesh Kishan of UMS Advisory, Inc., provide an overview of the RE & FM Outsourcing Market and address main waves of market maturity. In particular, they examine significant outsourcing deals.

Environmental Monitoring and Certification in Controlled Environments

(Whitepaper)

Environmental testing and monitoring programs are essential elements in pharmaceutical and medical device manufacturing. Companies must understand industrial sterilization and contamination control procedures to bring products to market on time and on budget. Steven Wieczorek of Microtest ...

Where and What to Test: From Purified Bulk Drug Substance to Sterile Liquid ...

(Whitepaper)

This white paper focuses on what many consider the most critical part of a biological drug product’s manufacturing life cycle: going from the purified bulk drug substance (“PBDS”) to the sterile final drug product (“FDP”). Specifically, the white paper discusses establishing the testing “where ...

SAP Support of the Healthcare Supply Chain’s Ongoing Effort to Ensure Patient...

(Whitepaper)

This white paper provides a detailed look at SAP’s support for the Center for Healthcare Supply Chain Research Blueprint for Data Management & Data Sharing. It also offers a summary of the Blueprint concepts and a review short- and long-term business improvement opportunities that can be gained ...

Selecting sample points for particle monitoring

(Whitepaper)

Choosing sampling points for continuous or near-continuous monitoring of airborne particles in an aseptic processing environment requires a compromise between two opposing needs: the drive for comprehensive data and the desire to lower costs. This white paper from Hach Ultra provides tips on ...

Residual Solvents by HT3 Headspace in Reference to USP 467

(Whitepaper)

Residual solvents in pharmaceuticals are defined as volatile organic chemicals that are used or produced in the manufacture of drug substances, excipients or in the preparation of drug products. Because residual solvents do not provide therapeutic benefits, they should be removed, to the extent ...

Online Reaction Monitoring of Inprocess Manufacturing Samples by UPLC

(Whitepaper)

Process Analytical Technology (PAT) is a critical component in manufacturing, relied upon to ensure product quality and improve process yields. In this white paper, Waters Corp. discusses the use of novel Waters technology for online reaction monitoring of inprocess manufacturing samples, which ...

Nanoparticles in Pharmaceutical Manufacturing

(Whitepaper)

The paper explores the rapidly expanding role and significant performance advantages of nanoparticles in pharmaceutical applications. It provides an overview of nanoparticle uses in applications including diagnostic products, product packaging and biomarker discovery, as well as an extensive look...

Selecting An Aseptic Fill/Finish Contract Manufacturer: Avoiding the Most ...

(Whitepaper)

Selecting and establishing an effective working relationship with an Aseptic Fill/Finish contract manufacturer can be a challenging task. The ramifications of making a poor decision can result in schedule delays, regulatory approval issues, and lost revenue.This white paper provides guidance on ...

Aseptic PAT and Particle Monitoring — from Snapshots to Continuous Feedback

(Whitepaper)

Particle monitoring is critical for maintaining aseptic conditions, but portable counters won’t help develop trending data. In this white paper, Mark Hallworth, pharmaceutical manager for Particle Measuring Systems, discusses continuous monitoring methods, how they’re evolving, and why they’re ...

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