MEDILOG Consulting Sprl specializes in activities related to the distribution of drugs, medical devices and food supplements.
MEDILOG Consulting Sprl is at your disposal to ensure the compliance of your activites with Belgian and European legislation in the field of pharmaceutical distribution.
As mentioned above, MEDILOG Consulting proposes offers its services in the fields of:
Wishing to specialize in distribution, MEDILOG Consulting is not active in the field of registration and management of marketing authorization for medicines but collaborates regularly with companies specialized in this field.
For its new customers, MEDILOG Consulting assure them to respect the Belgian and European regulation regarding distribution in all aspects:
Analyse their situation from a GDP perspective (authorisation, contract, procedures)
Create/adapt their quality manual ;
Train their staff ;
Validate their Technical and Quality Agreement (TQA) ;
Be their person of reference with health authorities in order to obtain the required authorisation.
For its regular customers MEDILOG Consulting takes care of:
Regulatory Monitoring ;
The function of Responsible Person GDP (drugs) ;
The function of quality manager for MEDDEV (medical devices) ;
The function of contact point for “RAS” (Rapid Alert System) with the FAMHP (7 days week 24 hours a day) ;
The function of local contact point “vigilance” (7 days week 24 hours a day) ;
The maintenance of their quality system ;
A regular audit of their process through KPI and thematic audits ;
An annual Quality Management Review with the direction ;
The relationship with authorities (FAMHP and FASFC) ;
The management of “Change Control” and “Validation master Plans" ;