Services
1. Site Management and Medical monitoring
We provide highly qualified and experienced Study Coordinators (SCs) and Site Management Associates (SMAs) to help support both principal investigators and sponsors. Through our SMO service, we provide principal investigators with trained SCs to assist with daily clinical trial activity and patient recruitment; and sponsors with experienced SMAs to provide clinical trial site management and ethics committee support. The services include, however not limited to:
2. Data Management
Our team is committed to providing quality clinical data management to support your drug development needs to get drugs to market as quickly as possible, so patients have access to drugs. We provide bespoke solutions tailored to your requirements and provide real time, faster access to data meaning faster decisions can be made to keep patients as safe as possible.
3. Data Analysis: SAS and biostatistics
Our team's global reach offers great flexibility and can be modelled to the customers needs regardless of the size of your team. We have the ability to scale up or down in accordance with your pipeline. Our statistical programmers turn un-interpretable data into something meaningful to make informed decisions, improving patient safety, demonstrating drug efficacy and getting drugs to market faster.
4. Medical Writing Services
Medical Writing is an integral part of clinical research and our team of specialist medical writers deliver accurate, timely, and cost-effective clinical and regulatory documents to the highest quality and scientific standards.
Our medical writers become an extension of your team by being responsive and flexible to your needs, using our expertise to transform your complex and diverse data into an accurate and evidence-based account of the clinical profile of your drug in relation to treatment and patient safety.