Prior to approving any clinical trial, the relevant global regulatory agency needs to be assured that the chemistry, manufacturing and controls elements have been appropriately considered and documented.
The dossier team at Arcinova has the knowledge and experience to advise and/or to prepare the CMC content of clinical trial applications directly from the relevant source data. This service can be accessed on a stand-alone basis or as part of an integrated CMC service. This service is also provided for clinical trials designed to study the absorption, metabolism and excretion of radiolabelled pharmaceuticals.
Bio SpainBioSpain 2018 will be attended by Nathalie Huther, Business Development Manager Europe.
Bio SpainDates: 25th - 27th SeptemberLocation: Seville, Spain
BioForwardThe BioForward event will be attended by Nathalie Huther, Business Development Manager Europe.
BioForwardDates: 4th OctoberLocation: Birmingham, UK
CPhI WorldwideCPhI Worldwide will be attended by Nathalie Huther, Business Development Manager Europe. Nathalie will be located at the DIT stand: 9J40
CPhI WorldwideDates: 9th - 11th OctoberLocation: Madrid, Spain