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Das Krebsregister Mecklenburg-Vorpommern (KRMV) comprehensively collects and analyzes data on cancer in Mecklenburg-Vorpommern. The aim is to continuously improve the quality of oncological care in the federal state. This is done through the comprehensive collection of cancer cases, their course and therapy.
The KRMV is divided into three independent institutions: Registerstellen, Treuhandstelle and Zentralstelle. This division ensures both the fulfillment of legal tasks and the protection of patient data. The Registerstellen are responsible for the collection and processing of data. The Treuhandstelle ensures the anonymity of patient data. The Zentralstelle coordinates the activities of the KRMV and is responsible for the evaluation of the data.
The KRMV provides data for research purposes and regularly publishes annual reports and interactive reports. These reports contain important information about the frequency of cancers, their distribution and the effectiveness of various treatment approaches. The data serve as a basis for the development of strategies for cancer prevention and treatment.
The KRMV offers training courses and quality conferences for reporting physicians and clinics. These events serve to improve the quality of the data and to promote exchange between the various actors in the field of oncological care.
The KRMV works on the basis of the nationwide Krebsfrüherkennungs- und -registergesetzes (KFRG) and the Krebsregistrierungsgesetzes M-V. It strives to continuously develop cancer registration in Mecklenburg-Vorpommern and to increase the benefits for patients, doctors and research. The reports are made electronically via a Meldeportal, which offers doctors, clinics and oncological centers the opportunity to securely transmit the required data.
