Aya Sabry

Regulatory Affairs

studying scientific and legal documents gathering, evaluating, organising, managing and collating information in a variety of formats ensuring compliance with regulations set by the Medicines and Healthcare products Regulatory Agency . maintaining familiarity with company product ranges planning, undertaking and overseeing product trials and regulatory inspections keeping up to date with changes in regulatory legislation and guidelines analysing complicated information, including trial data offering advice about company policies, practices and systems obtaining marketing permission outlining requirements for labelling, storage and packaging using a variety of specialist computer applications liaising and negotiating with regulatory authorities providing advice about regulations to manufacturers/scientists writing comprehensible, user-friendly, clear product information leaflets and labels ensuring that quality standards are met and submissions meet strict deadlines preparing documentation