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.
ProRelix Research’s medical writing capabilities range from Clinical Research, Regulatory, Pharmacovigilance to Publication.
ProRelix Research’s Regulatory Affairs services provide expert support in drug development programs.