To the attention of interested persons
The NAMMD training organised in the second half of 2011 will be conducted as follows:
1. Setup of the leaflet in accordance with the new QRD Guideline and its readability testing – 16 September 2011
2. Assessment of the chemical-pharmaceutical and biological documentation for medicinal products for human use – 23 September 2011
3. Legislative regulations on performance of clinical trials in Romania – 21 October 2011
4. Good Manufacturing Practice – 4 November 2011
5. Activities of the Competent Authority and of the MAH for implementation of provisions of the new European pharmacovigilance legislation – 11 November 2011.
For further details please contact Mrs. Laura Bodor: email@example.com