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5 Reasons to Work with Synteract For Your Pediatric Clinical Trial

5 Reasons to Work with Synteract For Your Pediatric Clinical Trial
20 November 2018

Whether you are looking for small scale support, assistance with a specific service, or complete study design and management, Synteract draws on extensive, end-to-end experience in helping clients efficiently navigate the complexities of pediatric trials and regulatory environments.

Following are five reasons to consider Synteract for your pediatric clinical trial.

  1. Challenges Still Remain for Pediatric Drug Development
    Although there has been significant progress in establishing the regulatory framework for pediatric drug development in the US and EU, many clinical, scientific, technical, and regulatory challenges still remain for pediatric product labeling. Pediatric clinical trials also pose challenges in recruitment, participation, and clinical trial design.
  1. Pediatric Center of Excellence
    Our recent acquisition of KinderPharm builds on our extensive experience in navigating complex pediatric regulatory environments, advanced pharmacometric modeling and clinical trial simulation technologies coupled with juvenile formulation and toxicology services. A dedicated, fully-integrated one-stop pediatric CRO for preclinical and clinical pediatric drug development, our mission at Synteract is to be your expert pediatric partner.
  1. Bringing Better Medicines to Life for Children
    With the goal to bring clinical trials to life to make better medicines available to children, we strive to apply the best available scientific, technical, clinical, and quality practices to serve the needs of patients and deliver value to our customers. We collaborate with international pediatric networks, opinion leaders, patient advocacy groups, and regulatory bodies key to pediatric development and pediatric success and capitalize on relationships with global partners invested in this patient population.
  1. “One Stop” Service Model
    Our integrated “one-stop” service model enables us to efficiently and cost-effectively advance pediatric products, across indications, through all the required stages of pre-clinical and clinical development. Synteract’s pediatric cross-functional team helps clients navigate complexities of pediatric research and provides tailored planning, and experienced technical and operational services to allow medicines to reach patients in need.
  1. Unique Expertise
    A comprehensive portfolio of pediatric development capabilities, combined with the talents and experience of our staff and leadership, delivers our clients a unique set of expertise and insight to tackle the most challenging of development issues. We draw on an extensive team of industry-leading pediatricians, PKPD scientists, and executives actively involved in the industry. We understand the level of compassionate and specialized clinical and regulatory expertise required in working with vulnerable pediatric populations and their families.

Want to learn more about how our pediatric clinical trial experts can help you? Contact Us


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