clinomic
Rethinking Critical Care
clinomic
Rethinking Critical Care
“Without any doubt, Mona represents a breakthrough in the care of all critically ill patients.”
– Univ.-Prof. Dr. med. Gernot Marx, FRCA
That’s exactly what Mona is for intensive care medicine: an integrated solution, all information, numerous intuitive applications, relief in your daily tasks and support in your decisions – all combined in one platform. And all of this fits seamlessly into your clinical workflow.
Mona – means for you
550 h time saved per bed
Mona reduces the administrative effort for documentation, handover at shift changes and during ward rounds by up to 30 minutes per shift and intensive care bed compared to analog fever charts. As a result, up to 550 hours of unproductive time per year and intensive care bed will be avoided. [1]
143 % ICU care capacity
Clinical studies demonstrated that telemedical consultations reduce the length of stay in the ICU by between 17% and 38%. [2] [3]. Mona enables GDPR-compliant, interdisciplinary telemedical consultation with internal and external specialists for intensive care.
26 % fewer transfers
Mona supports patient management in the hospital network and brings the expertise of intensive care physicians from various specializations to all locations. Such collaborations have the potential to prevent unnecessary transfers. In a clinical study on teleconsultations at the Einstein Clinic, transfers were reduced by 26%. [4]
Revenue assurance
Mona functions such as worklists, workflows, AI and other support tools ensure not only guideline-compliant care but also complete documentation of billable services. A clinical study showed that Mona reduces documentation errors by a factor of eight. [5]
Future-proof and sustainable
Sana Kliniken AG chooses Clinomic
Stefanie Kemp
Member of the Management Board of Sana Kliniken AG, Chief Transformation Officer (CTO)
What we stand for
Clinomic
We create solutions that have a lasting impact on the lives of our patients, the working reality of our users and the well-being of our society.
Focus on people
Doctors and nursing staff are our top priority. We develop products that optimally support you in the treatment of critically ill patients and ensure guideline-compliant care.
Sustainability
We support an intelligent, efficient, and resource-oriented digital transformation for the automation of administrative tasks, the comprehensive recording of all services provided, and legally compliant documentation.
Future-proof
Modular software architecture, integrated cyber security, cloud technologies, open interfaces, structured data, user-oriented design, AppStore, AI platform and much more secure your digital future.
What makes Clinomic stand out?
Practical solutions based on our own long-standing experience in intensive care.
Clinomic Group
Clinomic was founded in 2019 by intensive care physicians from RWTH Aachen University Hospital. With its roots in European intensive care medicine, medical digitalization and telemedicine, the company has been revolutionizing acute and intensive care medicine ever since.
Managing directors
Dr. med. Arne Peine (CTO), Georg Griesemann (CEO) and PD Dr. med. Lukas Martin (CMO)
Certifications
As a modern, digital MedTech company, we are committed to the highest quality and safety standards. Our certifications and our focus on data protection and regulatory compliance are the basis for the quality and safety of our products. Through our high standards and the continuous development of our products and services, we offer innovative and reliable solutions that meet all your needs.
ISO 27001: Information Security Management System
Information security is of crucial importance to you and to us. We are ISO 27001 certified, the international standard for the highest requirements for the protection of sensitive information. Through structured and constantly developing security processes, we minimize risks and ensure the protection of data – an essential basis for your trust in our solutions and services.
ISO 13485: Quality management
Our quality management system (QMS) is certified according to the international standard ISO 13485 and meets all the requirements of the European Medical Device Regulation (MDR). This ensures that our solutions, services and processes meet the highest quality requirements of a medical device manufacturer.
MDR (EU) certification
Our medical devices are Class IIa (software solutions) or Class I (Mona Terminal) MDR-compliant and meet the comprehensive requirements regarding safety, performance and regulatory compliance of the current Medical Devices Regulation (EU 2017/745). Accordingly our products can be used without any restrictions in the care of your patients.
C5 certificate
Clinomic HealthCloud – our cloud services – meet the high requirements of the C5 criteria catalog (Cloud Computing Compliance Criteria Catalog) of the Federal Office for Information Security (BSI). This demanding certification creates transparency and trust and guarantees you that your and your patients’ data is comprehensively protected in our cloud.
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