Our service covers the clinical supply process from clinical manufacture to drug destruction in quantities ranging from Phase I and compassionate use requests to large-scale Phase III/IV studies. It includes packaging, labeling, and distribution services for patient administration at investigational sites.
All activities above are guaranteed by GMP and GLP certification and processed according to local law.
Axon CRO, s.r.o.
Ševce Matouše 26
140 00 Praha 4
Czech Republic
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e-mail: [email protected]
www.axon-cro.com
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