Full Service Clinical Research

We offer expert support and management of clinical studies for pharmaceutical, biotechnology and medical device companies. Our fine-tuned clinical trial development processes enable us to manage your clinical programme from concept, through to marketing application if required. 

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Data Management

Our experience working with different platforms allows us to create the ideal eCRF for your requirements, which ultimately leads to you getting the data you need for your study. We offer a variety of different fully validated, user-friendly eCRF Platforms to suit both your needs and your budget.

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The CQA Company

Established in 2002, our Clinical Quality Assurance division facilitates optimal commercial efficiency in helping bring clients’ products to market. Our highly qualified team can deliver internal and external audits, support for inspections, QMS development and review, and QP services.

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Why outsource?

Accler8 Clinical Research brings together subject matter experts around the world, specialising in disciplines including clinical development, data management, project management, clinical quality assurance and regulatory affairs.

Outsourcing aspects of your clinical studies enables you alleviate budget pressures, by allowing you access to a range of subject matter experts, to utilise as and when you need them. Whether you need help with one aspect of a study, or end-to-end management, we can design an outsourcing model to suit you.

Speak to our team…

Discuss your requirements directly with our consultants for trustworthy, pragmatic advice.