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Drug Development & Delivery Article: April 2018

Optimizing the Application of In Vitro Test Methods for the Demonstration of Bioequivalence in Orally Inhaled Products

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PMPS Article (Samedan): February 2018

Demonstrating Bioequivalence of Orally Inhaled Products Safe and cost-effective treatments for respiratory diseases are facing a g…

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White Paper: February 2018

Optimising the application of in vitro test methods for the demonstration of BE in OIPs

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PMPS Article (Samedan): February 2016

Go With the Flow – Testing Inhaled Generics Increasing global requirements for efficacious, inexpensive products to treat re…

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Inhalation Article: April 2015

Comparison between in vitro performance of the Child “Alberta” Idealized Throat and Ph.Eur./USP induction port for the deliver…

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ONdrugDelivery Article: 2015

Improving the Realism and Relevance of Mouth-Throat Models for Inhaled Product Testing In this piece, Mark Copley, Sales Director …

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ONdrugDelivery Article: December 2015

A New, Advanced High-Throughput System for Automated Inhaler Testing

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Innovations in Pharmaceutical Technology Article (Samedan): December 2015

Testing Inhaled Generics New product-specific FDA guidance and USP monographs support the development of popular inhaled products….

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Pharmaceutical Technology Q&A 2014

Exploring newly introduced methods for testing metered dose inhalers with add-on devices The role of add-on devices and how they a…

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OINDP News Q&A 2014

Implications of the introduction of a new US Pharmacopeia (USP) monograph for Fluticasone Propionate (FP) testing

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Pharm Bio World Article 2014

Nebulisers – Understanding the Regulatory Framework and Testing Requirements

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