TopPharm Consulting

Company provides
regulatory affairs services in EU for medicinal product (CTD dossier audits and
medical writing, in and out-licensing, management of authorization, renewals
and variation procedures, pharmacovigilance services and PIL readability
testing services), medical devices (clinical evaluation reports, authorization
of products and consultancy), food supplements, FSMPs and cosmetics including
medical writing, eCTD publishing for EU and GCC region with consultancy on
local requirements. Former authority experts.