CCDRD AG is capable of taking over the responsibilities of the Responsible Person Pharmacovigilance on behalf of the sponsor to fulfil European and national pharmacovigilance reporting requirements for clinical trials as defined in the Regulation (EC) No 726/2004, Directive 2001/83/EC and as amended by the Directive 2001/20/EC.

Service offered:

• Responsible Person Pharmacovigilance on behalf of sponsor