CHAPTER 2

GOOD CLINICAL PRACTICE FOR THE DESIGN, CONDUCT, RECORDING AND REPORTING OF CLINICAL TRIALS
SECTION 3

THE SPONSORS
Article 7
1
A sponsor may delegate any or all of his trial-related functions to an individual, a company, an institution or an organisation.
However, in such cases, the sponsor shall remain responsible for ensuring that the conduct of the trials and the final data generated by those trials comply with Directive 2001/20/EC as well as this Directive.
2
The investigator and the sponsor may be the same person.