Regulatory Affairs

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Xania has a highly qualified and experienced inhouse team of dynamic scholars who devote quality time and intelligence in preparation of Technical Dossiers required for registration of products in various Countries of the world. The team is led by a well experienced Team Leader possessing over 30 years of experience in the required field. We are well equipped to prepare CTD and ACTD Format of dossiers as per the international guidelines of:-

WHO GMP

TGA Australia

PICs Countries

EU GMP Europe

SAHPRA South Africa

ANVISA Brazil

Singapore Food Agency

US FDA

Department of Health Abu Dhabi

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