Clinical Data Management

Managing the labeling process for clinical trials is extremely demanding. This can involve hundreds of thousands of patients in several countries with patient guidelines in multiple languages.Documenting the trials needs to be a smooth, precise, and fast process with traceable documentation to ensure patie...

Quotient Sciences has almost 30 years of experience developing a breadth of pharmaceutical formulations across a range of indications. Our innovative approach to formulation development integrates drug product development with clinical evaluation, combined with our experience with over 1,000 molecules at a...

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. Our statisticians have extensive experience in various phases of clinical trials and different therapeutic areas. Working on a project, our team see...

At ProRelix Reseach wiith the unique blend of medical writers comprising of doctors, pharmacists, scientists and grammar experts, ProRelix provides medical writing services from essential documents such as study synopsis and protocol, clinical study report (CSR), investigator’s brochure (IB) informed conse...

Our in-house cost-effective Digital solutions keep you connected at every stage, no matter where in the world your studies run.

Our Digital Solutions are integrated solutions, Regulatory compliant, and it can handle all type of clinical trials.

Our Digital Solution portfolio consist o...

Our expert teams help eliminate delays by leading the way from recruitment strategies, medical writing, and clinical logistics, all the way through the regulatory process. 

Our in-house eClinical technologies keep you connected at every stage, no matter where in the world your studies run. A...

• Supervision of IBs, protocols and related documents • Initiation and follow-up of clinical trials • Selection and contact of CROs