C&R Research


C&R Research is a leading clinical trial company with 28 years of experience, conducting 1,800 clinical trials across 59 countries. They specialize in full-scale clinical services, including regulatory affairs, trial management, data management, biostatistics, pharmacovigilance, and quality management, aiming to pioneer new pathways in clinical trials and drive success in the industry.

Industries

Clinical Trials
Health Care
Medical
Pharmaceutical
Pharmaceutical Manufacturing

Nr. of Employees

medium (51-250)

C&R Research


Products

Full-Service Clinical Research Organization

Comprehensive one-stop clinical trial solutions spanning initial planning to final regulatory submission, backed by over 1,800 successful clinical trials and regulatory procedures.

C&R Research

End-to-end clinical research organization providing full-scope clinical trial services, pivotal trials, and non-registrational trials.

Phase 1 ~ Phase 3 Trial Management

Customized clinical trial management solutions from Phase 1 to Phase 3 covering planning, execution, data management, and final report writing.

Medical Advisor Service

Professional medical advisory and consulting service combining medical knowledge and clinical experience for clinical trials, ranging from scientific design to data interpretation.

Improved New Drugs Clinical Trials

Specialized clinical trials to enhance therapeutic value, formulation improvements, optimization of administration methods, and addition of new indications.

Central Nervous System Clinical Trial Solutions

Customized clinical trial solutions optimized for therapeutic development in central nervous system disorders such as Alzheimer's disease, Parkinson's disease, multiple sclerosis, and epilepsy.

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Services

Medical and scientific advisory services to inform study design and clinical strategies.

Operational and regulatory support for early clinical studies including protocol development and study execution.

End-to-end trial operations including site management, monitoring, and study coordination for regulatory and non-regulatory trials.

Support for regulatory strategy and submission activities related to clinical development and approvals.

Study data collection, validation and preparation of analysis-ready datasets.

Statistical planning, sample size determination and data analysis for clinical studies.

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Expertise Areas

  • Clinical trial management
  • Early-phase clinical development
  • Regulatory affairs for approvals
  • Clinical data management
  • Show More (6)

Key Technologies

  • Electronic data capture (EDC) and eClinical platforms
  • Clinical trial management systems (CTMS)
  • Statistical analysis methods and estimand frameworks
  • Clinical imaging workflows
  • Show More (4)

News & Updates

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