The information in the protocol, investigatora#39;s brochure and ICF, particularly that on possible adverse events, must be consistent. In Europe, personal data are subject to strict regulation (Directive 95/46/EC).1 The ICF must tell subjects who willanbsp;...
|Title||:||The Textbook of Pharmaceutical Medicine|
|Author||:||John P. Griffin|
|Publisher||:||John Wiley & Sons - 2009-10-15|