Medicinal products
The obligation to establish a “Publicly accessible professional information service – VPOIS” results from Act No. 378/2007 Coll., Section 33(3)(g)(1).
Healthcare professionals are provided with information from the Summary of Product Information (SPC) (in accordance with Section 2a of Act No 40/1995 Coll. on Advertising Regulation). Other information, including information from the Package leaflet (PIL), is intended for the general public.
Information on registered medicinal products:
Pharmacovigilance and quality
To report suspected adverse reactions or product quality complaints in relation to registered medicinal product distributed by IEM Allergy s.r.o., please use this link: Email: iemallergy-ds@qmfocus.com