Only half of cancer medicines approved by the European Medicines Agency in 20202023 are available in EU countries (on average) Average time from EMA approval to patient access: 586 days, with major variation between Member States Access to biomarker testing, essential for personalised cancer treatment, is inconsistent across Europe Reducing disparities in access to medicines and diagnostics is essential to ensure innovation benefits all patients, wherever they live
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Perhaps theres something we can change on the pre-op form or something we could do that would make your life easier for preoperative assessment
Your healthcare team can review your complete medication list for potential interactions, assess whether dose escalation is appropriate, evaluate your injection technique, and determine if additional investigations such as thyroid function tests or metabolic panels are warranted
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