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.
BioNH's 2019 Annual Dinner Meeting & Innovation CelebrationThe annual dinner meeting and innovation celebration will be attended by Masha Kononov, Senior Director Emerging Pharma US.
BioNH's 2019 Annual Dinner Meeting & Innovation CelebrationDates: 7th FebruaryLocation: New Brunswick, NJ
CED Life ScienceThe CED Life Science Conference will be attended by Masha Kononov, Senior Director Emerging Pharma US and Gail Frey, Senior Director Key Accounts US.
CED Life ScienceDates: 16th - 17th FebruaryLocation: Raleigh, NC
Drug Delivery & Formulation SummitThe DDF Summit 2019 will be attended by Dr. Nathalie Huther, Business Development Manager Europe.
Drug Delivery & Formulation SummitDates: 11th - 13th MarchLocation: Berlin, Germany