Booklet Labels Give Pharma and Medical Devices Room for Full Instructions Amid MHRA CE Mark Consultation
Regulatory expectations for pharmaceutical and medical device labelling are evolving, with the MHRA placing greater emphasis on traceability, transparency, and pre-market documentation. As part of ongoing consultations around CE marking and post-Brexit frameworks, many products now require significantly more on-pack information than in previous years. This includes detailed instructions for use, multilingual warnings, Unique Device […]