Our Services
As your clinical research organization (CRO), we listen and collaborate to tailor a project plan that strategically adapts our services to support your specific project needs. Whether needed for a global, full-service offering, a standalone service like clinical data management services, pharmacovigilance services/ drug safety services, medical writing services, functional service provision of resources, or consulting, our team of experts is here to help.
With increasing drug development cost, sponsors and their selected clinical research organizations (CRO) need to work smarter than before. We know your goal is getting to successful regulatory submission & acceptance by regulatory authorities like US FDA, CDSCO, MHRA, EMA, TGA, etc. and we package our services to help you get there.
Our expert project team proactively delivers optimal solutions to accelerate project delivery. We not only focus on the ‘what’ but also the ‘how’, allowing our clients to concentrate on decisions and strategies.
Clinical Research
At ProRelix Research we focus on Quality, Ethics and Well-being of the clinical trial subject.
Data Management & Statistics
At ProRelix Research we are a team of experienced people who are well aware of 21 CFR, HIPAA, ICH GCP compliance to provide clinical data management services.
Medical Writing
ProRelix Research’s medical writing capabilities range from Clinical Research, Regulatory, Pharmacovigilance to Publication.
Regulatory Affairs
ProRelix Research’s Regulatory Affairs services provide expert support in drug development programs.
