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