- Vouliez-vous dire
- regulations
Résultats de la recherche - 4 results
Identification of Flavouring Substances of Genotoxic Concern Present in E-Cigarette Refills
alert for genotoxicity in at least one of the two (Q) SAR models. For these substances, genotoxicity data was collected from previous European safety evaluations in different regulatory domains (e.g. by ...
Advanced Methods for Dose and Regimen Finding During Drug Development: Summary of the EMA/EFPIA Workshop on Dose Finding (London 4-5 December 2014).
issues in drug development, as illustrated by high rates of late-stage attritions in clinical development and postmarketing commitments required by regulatory institutions. In an effort to shift the ...
Commentary on the MID3 Good Practices Paper.
the development and regulatory assessment of medicines. In the 2011 EMA — European Federation of Pharmaceutical Industries and Associations (EFPIA) Workshop on Modelling and Simulation, European ...
Regulatory panel discussion. An interactive panel discussion with key authoritative figures from various European regulatory agencies focusing on the regulation of the biologics industry.
Affect an challenge CHALLENGES Discussion European Industries Industry ON production regulation Regulatory use Service: Qualité des vaccins et produits sanguins Kwaliteit van vaccins en bloedproducten ...