Sarah Cowlishaw is an associate in the life sciences group in the London office of Covington & Burling LLP. Her practice focuses on life sciences regulatory and commercial law for pharmaceutical, medical device, food and consumer products. Her advice on general regulatory matters includes borderline determinations, food classifications, adverse event and other reporting obligations, manufacturing controls, and labelling and promotion. On the commercial side, she advises on the full range of agreements that span the product life cycle in the life sciences sector. Her expertise includes clinical trial agreements, manufacturing and supply agreements, distribution and other marketing agreements and regulatory services agreements. She also advises on regulatory aspects of corporate and commercial deals, particularly regulatory due diligence.