Ciara is a regulatory and compliance specialist advising clients on EU and Irish regulatory matters applicable to medical devices, medicinal products, food law and cosmetics throughout their entire life cycle. This includes assisting clients in classification of their products, establishment of a pathway to authorisation and marketing of their products in the European Union (including related regulatory obligations), pharmacovigilance obligations, promotion and marketing of products, sales agreements, clinical trial agreements, adverse event reporting, product withdrawals, data privacy obligations, conduct of compliance and anti-bribery investigations, and regulatory due diligence. She also challenges national authority and EU institution decisions concerning classification and marketing of medicinal products and medical devices.

Ciara assists life sciences clients in the preparation, drafting and review of numerous agreements, including clinical study agreements, pharmacovigilance agreements, CRO agreements, European authorised representative agreements, distribution agreements, and sales and promotion agreements.