
THE CLARA
TRAINING CYCLE
The 4th session in the "Development of a Biological Agent, from the Bench to the Bedside: regulatory aspects" training cycle (entitled "Clinical Evaluation of Nano-Objects") will take place in October 2009.
These free training sessions are aimed at providing practical guidance to professionals who are involved in the development and commercialization of biological agents generated by nanotechnology research programs.
The training takes a detailed look at the regulatory and logistical framework in the development of a biological, with a view to facilitating transfer to man:
- quality management systems and how to implement them
- safety management in toxicology and preclinical proof-of-concept work
- procedures in first-in-man trials.
The courses are open to anyone from academia or industry involved in the development of medicinal products for human use.
To register, please contact:
Leticia Lobo Luppi
Canceropôle Lyon Auvergne Rhône Alpes / HCL
Tel: +33.4.37.90.17.18
Fax: +33.4.37.90.27.03
lloboluppi@canceropole-clara.com
Venue:
International Agency for Research on Cancer
50 cours Albert Thomas, F-69008 Lyon, France.
For more information
