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BENEFITS
Preclinical development runs from the selection of a promising drug to regulatory
submission of all generated data. Several, quite diverse disciplines are involved
such as general toxicology, reproductive toxicology, pharmacokinetics, and metabolism.
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.
By teaming up with ADMERITOX, YOU as the client may expect:
- focus on 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, thus providing continuity all the way to preparation
of the final dossier for a product
- tangible products: quality documents
at a competitive price within pre-agreed timelines
A COLLABORATION
WITH A FOCUS ON YOUR BENEFIT
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