Sat.Sep 02, 2023

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In Equal Measures: The Importance of Excipient Quality

PharmaTech

Excipients should be treated equally when it comes to quality management, risk assessment, and testing.

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Formulating with Coprocessed Excipients: Current Trends

PharmaTech

Coprocessed excipients save time and cost while improving performance in a widening array of dosage forms.

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Clearing Up Confusion in Inspection Terminology

PharmaTech

Audits and inspections both assure that requirements have been fulfilled and whether documented proof is available, says Siegfried Schmitt, vice president, Technical at Parexel.

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Mixing Systems for Ultra-High Viscosity Materials

PharmaTech

The ROSS line of Double Planetary Mixers are fully customized and engineered for efficient processing of medical-grade silicone formulations in a portable workstation.

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European Clinical Supply Planning: Balancing Cost, Flexibility and Time

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Size Exclusion Chromatography Columns

PharmaTech

Waters Corporation’s XBridge Premier GTx BEH size exclusion chromatography (SEC) columns are designed to improve analysis while lowering the cost of gene therapies.

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Knowledge as the Currency of Managing Risk: A Smart Investment for Patients

PharmaTech

Recent research and perspectives shed light on an opportunity to better connect risk and knowledge through improved integration of systems.

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Accelerating Clinical Trials in the EU

PharmaTech

The ACT EU initiative aims to develop the European Union further as a competitive centre for innovative clinical research.

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Billions of Reasons to be Buoyant

PharmaTech

Pharma's ability to continually reinvent itself will be critical in growing future business operations.

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Clinical Trials and their Impact on the Pharma Industry

PharmaTech

There are many promising trials in the pipeline that may bring big news for major therapeutic areas.

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Preserving Process Integrity: The Importance of Equipment Cleaning

PharmaTech

A structured cleaning procedure is essential to ensure the effective cleaning of equipment.

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How Machine Learning Drives Clinical Trial Efficiency

Clinical trial data management is increasingly challenging as studies grow in complexity. Quickly accessing and analyzing study data is vital for assessing trial progress and patient safety. In this paper, we explore real-time data access and analysis for proactive study management. We investigate using adverse event (AE) data to monitor safety and discuss a clinical analytics platform that supports collaboration and data review workflows.

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The Future is the Present: Artificial Intelligence in Pharmaceutical Manufacturing

PharmaTech

FDA is anticipating how AI may advance manufacturing and improve supply chain security.

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Harnessing the Power of Oncolytic Viruses

PharmaTech

Tumour-infiltrating lymphocyte (TIL) therapies offer a new route to target cancer.

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Booster Shot for Pharma

PharmaTech

European vaccine manufacturing is being boosted with high level investments.

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Improving Manufacturing Flexibility with Modules

PharmaTech

Modular facilities allow for a certain amount of flexibility and reconfiguration options.

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Unlocking Excellence: How Catalent Is Transforming Japan’s Clinical Research

Planning on running clinical trials in Japan? How can you reliably supply these studies? Discover Catalent’s clinical supply packaging facility in Shiga, Japan. Strategically located between Tokyo and Osaka, and one of largest in Japan, this 6,000 square meter facility offers comprehensive services including primary and secondary clinical packaging and labelling, comparator sourcing, cold chain storage, local and global distribution, local language support and white glove service to support stud