We provide specialist services to the Pharmaceutical Industry

We are a flexible organisation with a team of experienced professionals in

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Regulatory Affairs

Our regulatory team has everything you need to achieve successful agency dialogue, plan your regulatory strategy, achieve timely submissions and approvals. Whatever your regulatory need, we’re here to help.

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Pharmacovigilance

Our senior safety scientists are experts in designing, implementing and leading full risk management and pharmacovigilance (PV) programmes

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SAS Professionals

As authorized trainers in CDISC SDTM and ADaM, we provide training, hands-on support, and expertise about requirements, processes, and systems to support CDISC requirements.  Our CDISC specialists are experienced in implementing standards for small, medium, and large pharmaceutical companies.

Our team

Our team of experts is dedicated to providing high-quality, practical, responsive, and cost-effective services to support biotechnology and pharmaceutical companies.

How can we help you today?

Clinical Trial Regulation

Development/
R&D Phase

Post Approval/
Post Licensing

Our vision is to give every client the best results with our team's knowledge, abilities, reliability, and expertise.

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