From First-in-human studies to RWE data acquisition for post-marketing surveillance, our team of experts are with you at every stage. Leveraging our data driven insights, and our extensive domain knowledge in designing trials, we support your trial, assuring you the utmost data quality standards.

Our broad range of study expertise includes

Early Phase:

Phase 1 – First-in-human studies

Phase IIa – Proof-of-concept studies

Pharmacokinetic and Pharmacodynamic studies (PK/PD)

Bioequivalence and Biosimilar studies

Observational Studies:

Our experiences team supports a broad range of observational studies including

Case Control Study

Cohort Study (Prospective & retrospective)

Case Reports

Case Series

Cross-sectional studies

Investigator Initiated Trials:

We have 20+ years of experience offering end to end solutions for Investigator Initiated Trials conducted by individual investigators, Academic research institutes and Hospitals. From writing the protocols, to setting up the database and data analysis we support the Investigators successfully conduct the clinical trials.

Our range of services include:

Real World Evidence Studies:

RWE stands for Real-World Evidence studies. These are a type of observational study that gathers data on health outcomes from real-world settings rather than controlled clinical environments. RWE studies aim to complement traditional clinical trials by providing insights into how medical products (drugs, devices, treatments) perform in everyday clinical practice. They focus on assessing safety, effectiveness, and patterns of use in diverse patient populations that may not be fully represented in clinical trials.

Types of RWE Studies:

• Retrospective cohort studies: Analyze data from past medical records to assess outcomes associated with different treatments.

• Prospective cohort studies: Collect data over time from current patients to evaluate long-term outcomes.

• Pragmatic trials: Implement clinical interventions within routine clinical practice to assess real-world effectiveness.

• Comparative effectiveness research (CER): Compare different treatment options to determine which one works best for particular patient populations.

Patient Surveys:

These types of studies help us gaining more insights directly from the Patients. Celerius CR helps our clients choose from a set of pre-defined templates from our database, cutting down the time involved by 13%. Our range of services include

Patient reported outcome studies (Manual / electronic?

Patient Preference studies

Patient Satisfaction Studies

Patient Experience Studies

Remote Health Monitoring Surveys