Medical Resources
Medical Resources
ASCVD and heart failure
Psoriasis and hidradenitis supparativa
CML, myelofibrosis and more
Breast Cancer, RLTs, GEP‑NETs
PsA, axSpA, nr-AxSpA
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Peer-led education designed to keep you up-to-date with the latest scientific developments in your specialty. Access clinical pearls and guidance from respected experts to translate the science into practical applications for your clinic.
Programs and resources
We see treatment and management as two parts of the whole picture in patient care. That’s why we offer a range of support programs and resources to help clinics and patients get the most from our medicines.
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Adverse Events Reporting
Suspected Adverse Drug Reactions (side effects) or medication errors may be reported using the Malta Medicines Authority ADR reporting form, which is available online at http://www.medicinesauthority.gov.mt/adrportaland sent by post or email to: P: Pharmacovigilance Section at Post-Licensing Directorate, Malta Medicines Authority, Sir Temi Żammit Buildings, Malta Life Sciences Park, San Ġwann SĠN 3000. E: [email protected] Healthcare Professionals may also report any adverse events associated with the use of Novartis products to Novartis Pharma Services AG, Representative Office Malta, by phone on +356 21222872, online on https://www.novartis.com/reportor by e-mail at [email protected]