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BENEFITS

Preclinical development runs from the selection of a promising drug to regulatory submission of all generated data. Preclinical development involves numerous and quite diverse disciplines like bioanalysis, pharmacokinetics, metabolism, general toxicology and reproductive toxicology. The long preclinical development life cycle may be associated with numerous unexpected events and results, that have to be recognized at an early stage and adequately dealt with. Your organization needs all the experience, expertise and commitment it can get to make the "running of the gauntlet" as fast and as smoothly as possible.

By teaming up with ADMERITOX, YOU may expect:

  • focus and first priority to your specific needs;
  • input based on extensive experience and expertise in ADME and safety testing, obtained in several therapeutic areas and for several routes of administration;
  • all-round support in every aspect of preclinical development of your product, thus providing continuity all the way to the final dossier;
  • tangible products: quality documents at a competitive price within pre-agreed timelines.