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International Day of Women & Girls in Science

International Day of Women & Girls in Science

Honor women’s significant achievements in science and place a much-needed focus on girls entering Science, Technology, Engineering, and Mathematics (STEM) careers.

Utilising CROs for Effective Planning and Execution of Clinical Development

Utilising CROs for Effective Planning and Execution of Clinical Development

Ashley Hunter and Anna Yanaeva led an engaging discussion on the importance of “Utilising CROs for Effective Planning and Execution of Clinical Development”.

Writings with molecules and standards as main characters

Writings with molecules and standards as main characters

Clear communication is essential to drug development. At Aixial Group, our experienced medical writers know how to turn complex scientific data into clear, accurate documents.

Atomising cancer

Atomising cancer

Breakthrough — Radiopharmaceutical therapy represents a novel approach to treating cancer, utilising radioactive atoms to target and destroy malignant cells with precision, without affecting the patient’s healthy tissues.

Breast Cancer and Aixial Group’s Expertise

Breast Cancer and Aixial Group’s Expertise

In recognition of Breast Cancer Awareness Month, Ashley Hunter, Head of Strategic Development and Delivery…

Conflict of Interest in Clinical Trials 

Conflict of Interest in Clinical Trials 

One of the biggest challenges for researchers today is the threat of a conflict of interest in clinical trials (COI).

What Are The 4 Phases Of Clinical Trials?

What Are The 4 Phases Of Clinical Trials?

Clinical trials are designed to make sure that new treatments are better than existing ones. To do this, trials are structured by a framework that is made up of phases.

What Are Decentralised Clinical Trials? 

What Are Decentralised Clinical Trials? 

Decentralised clinical trials are a type of trial design used by studies to collect data from their participants. How data is collected can impact the trial’s efficiency, accuracy, and overall success and outcome.

How to prepare effective regulatory documents?

How to prepare effective regulatory documents?

Insights from Matilde Thye Kveiborg, Director of Medical Writing and Tanja Jensen, Senior Medical Writer

Demonstrating product value from multiple endpoints in rare disease trials

Demonstrating product value from multiple endpoints in rare disease trials

Rare diseases are often multifaceted, and a single endpoint is often not sufficient to fully describe treatment

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