Medical devices


Clinical trials Phase III - Phase IV. Observational studies

Entry into force of the New Regulation Sanitary Products 745/2017

  •      Scientific and medical writing: Protocols and Bibliographic reviews.
  •      Design of Data Collection Notebooks (CRDe)
  •      Monitoring
  •      Selection of centers and researchers.
  •      Procedures with CEICs, CCAA and AEMPS.
  •      Biostatistics
  •      Publications


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