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Bioavailability Enhancement Solutions

Bioavailability Enhancement Solutions

Bioavailability Enhancement Solutions

Bioavailability Enhancement Solutions

At Almac, we understand poor solubility remains one of the most persistent challenges in drug development. It is fundamental to understand the characteristics of an API to maximise a formulation’s solubility, stability and therapeutic impact.

Our bioavailability enhancement solutions are designed to overcome these challenges through proven technologies and extensive analytical data.

A Seamless Path to Clinical Success

At Almac, we bridge the gap between drug substance and drug product. From pre-formulation all the way to GMP manufacture, trust Almac to transform your drug product’s potential into a clinical-ready solution.

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Our Capabilities:

Single Partner Approach

Providing a fully integrated approach from a single source ensures that the formulation and processing knowledge gained throughout the development phase is effectively transferred for a seamless experience.

This end-to-end, integrated process means access to our proven technology, facilities and expert pharmaceutical development teams.

Meet our experts

James Hurst

James Hurst

VP of Operations & Charnwood Site Head, Almac Pharma Services

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Sander van den Ban

Sander van den Ban

Director of Operations, Manufacturing, Almac Pharma Services

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Manas Tilekar

Manas Tilekar

Associate Director of Formulation Development, Almac Pharma Services

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Conor Long

Conor Long

Associate Director of Manufacturing Science & Technology, Almac Pharma Services

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Jonathan Loughrey

Jonathan Loughrey

Director of Chemical Development, Almac Sciences

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Terry Ernest

Terry Ernest

Director of Manufacturing Science and Technology, Almac Pharma Services

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