Articles by Trevor Page - Pharmaceutical Technology

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Articles by Trevor Page

Trevor Page


Trevor Page is Group Technical Director at GEA Pharma Systems.

Articles
Continuous Manufacturing—the Future of Pharmaceutical Manufacturing
August 1, 2014

Continuous manufacturing is key to the future of pharmaceutical manufacturing.

Through-Vial Impedance Spectroscopy: A New In-Line Process Analytical Technology for Freeze Drying
April 2, 2014

A new process analytical technology based on impedance spectroscopy has potential applications for characterizing product attributes during the freeze-drying process.

Freeze Drying: The Experts' View
April 1, 2012

Lyophilisation is often necessary for pharmaceutical products to improve stability or shelf-life. However, the process can present difficulties, particularly when scaling up from the laboratory to commercial production. We bring experts together to discuss best practices for developing a lyophilisation process, including quality by design (QbD) and design space.

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Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
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Expedited reviews of drug submissions
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Reducing drug shortages
70%
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Protecting the supply chain
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Expedited reviews of drug submissions
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More stakeholder involvement
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View Results
Eric Langerr Outsourcing Outlook Eric LangerTargeting Different Off-Shore Destinations
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerAsymmetric Synthesis Continues to Advance
Jill Wechsler Regulatory Watch Jill Wechsler Data Integrity Key to GMP Compliance
Sean Milmo European Regulatory WatchSean MilmoExtending the Scope of Pharmacovigilance Comes at a Price
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