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 patient ...

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

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 all ...

You need data rapidly to make crucial decisions during a study. Faster data means we can provide our customers with earlier interim data and interim PK reports for on-study dosing and formulation decisions.
We understand on-study changes to early phase study designs and dosi...