Aepodia – Your Preferred Partner in Early Phase Clinical Trials : PARTNER IN FARLY PHASE®

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    • Scientific Consultancy
      • From preclinical and clinical drug development plans up to proof of concept
      • Biomarker recommendations and implementation
      • Preclinical and clinical due diligence
      • Translational scientific consulting services
    • Clinical Operations
      • Phase I/II project management and clinical strategy
      • Study management and reporting
      • Study monitoring
      • Clinical data management
      • Medical writing
      • Site assessment and audits
      • Paediatric trials
    • Pharmacovigilance
      • Safety and pharmacovigilance
      • Strategic consulting support
    • Regulatory Scientific Support
      • Drug and medical device submission
      • Regulatory EMA and registration support
      • Regulatory submission package

Paediatric trials

Aepodia can help you to develop a paediatric development strategy in compliance with European Regulation (EC) No. 1902/2006 by:

  • designing your paediatric trials;
  • conducting your feasibility analysis;
  • writing your study protocol and informed consent document taking into account the specific characteristics of paediatric populations; and
  • setting up, coordinating and monitoring your trial.
PARTNER IN FARLY PHASE®
  • Rue Louis de Geer, 6 • B-1348 • Louvain-La-Neuve • Belgium
  • Tel: +32 (0) 10/39.20.11 • Fax: +32 (0) 10/39.20.99 • info@aepodia.com • Disclaimer • Cookie Policy
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  • Home
  • About us
    • Company Profile
    • Board Members
    • Vision and Mission
    • Our values
  • Services
  • Expertise
    • Our R&D projects
    • Therapeutic areas
    • An international footprint
    • Case studies
  • Partnership
    • Members
    • Partners
  • News
    • News
    • Publications
  • Contact