Clinical Research Services
Post-Marketing Research

Clinical Research Services

(Drugs & Medical Devices)

In order to effectively bring breakthrough therapies to market across a wide range of therapeutic areas, our clinical research teams of professionals bring the skills and experience you need to ensure the safety and efficacy of your consumer healthcare products.

 Clinical Research Services

(Drugs & Medical Services)

  • Protocol feasibility and design

  • CRF and eCRF Development

  • Clinical supplies

  • Patient recruitment

  • Clinical monitoring

  • Risk-based Monitoring

  • Research Coordination

  • Regulatory affairs

  • Data management

  • Biostatistics

  • Medical writing

  • Pharmacovigilance/Vigilance

  • Vendor Management

  • Project Management

Post-Marketing Research

We offer comprehensive development in the full range of Regulatory, Observational, and Real-World evidence research so that you can fully demonstrate the safety, effectiveness, and quality assurance of your product.

Post-Marketing Research

Registries & Observational Studies

Epidemiological Studies

Medical Writing

Research Coordination

Early planning for post-approval research



Our experts who have significant work experience in clinical research development, work closely with our clients to develop customized plans that increase efficiency and reduce the risk of their product’s value, provide regulatory intelligence, and continuous support of their product development through our full range of services.


  • Clinical Development Plan design

  • Regulatory strategy and submission

  • Pharmacovigilance & Vigilance

  • Data Management & Statistical Analysis

  • Publication Support

  • Medical devices

  • Medical & Scientific Affairs

Best Services for your needs

World Class Complex Clinical Drug Development