Definitions

This subtopic focuses on definitions in the context of drafting for contracts. For information on boilerplate clauses in commercial business-to-business agreements, see: Boilerplate clauses—overview. For information on boilerplate in business-to-consumer contracts, see Practice Notes: Boilerplate clauses in business-to-consumer contracts—general principles and Boilerplate clauses in business-to-consumer contracts—specific clauses. For information on commercial clauses for business-to-business contracts, see: Commercial clauses—overview.

The definitions and interpretation clause of an agreement should include all of the individual defined terms that are included in an agreement and all of the provisions that are to apply to the general interpretation of an agreement and, if necessary, of certain phrases used with it. The defined terms and the interpretation provisions will normally be set out in two

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Life Sciences weekly highlights—4 December 2025

This week's edition of Life Sciences weekly highlights includes analysis by Bird & Bird of new MDCG guidance on the interplay between the Medical Devices Regulation (MDR) and the EU AI Act for AI-enabled medical devices, providing both EU and UK perspectives, and analysis by Mishcon de Reya of recent ASA decisions on misleading claims in the beauty industry. Also included is news that the Commission announced that the first four European Database on Medical Devices (EUDAMED) modules will become mandatory from 28 May 2026, and has published results of its second survey on EU medical device market availability, as well as news that the government has announced a UK-US pharmaceuticals deal, establishing a preferential tariff framework for medicinal products, NICE announced that cost-effectiveness thresholds for new medicines will rise from April 2026, the EU Member State Coordination Group on Health Technology Assessment (HTACG) adopted its 2026 Health Technology Assessment Work Programme. Further news includes the Council of the EU’s agreed position on the Critical Medicines Act and EFPIA’s response and news that International Council for Harmonisation (ICH) has adopted three final pharmaceutical guidelines and endorsed three draft guidelines, the ABPI published its annual clinical trials report showing a 25% decline in UK commercial clinical trial recruitment, the Science, Innovation and Technology Committee launched an inquiry into the potential harms associated with hair and beauty products, and the EU has launched new health crisis preparedness and response plan, among other stories.

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