<ul><li>studying scientific and legal documents to check they meet legal requirements.</li><li>gathering, evaluating, organising, managing and collating information in a variety of formats.</li><li>submitting information and responding to queries from bodies such as the Medicines and Healthcare products Regulatory Agency (MHRA).</li><li>maintaining familiarity with company product ranges.</li><li>planning, undertaking and overseeing product trials and regulatory inspections.</li><li>keeping up to date with changes in regulatory legislation and guidelines.</li><li>offering advice about regulations, company policies, practices and systems.</li><li>obtaining marketing permission.</li><li>outlining requirements for labelling, storage and packaging, and approving information leaflets and labels.</li><li>liaising and negotiating with regulatory authorities.</li></ul>

Regulatory Affairs Executive