Introducing a communication platform for accountable and transparent data processing in medical research (Preprint)

BACKGROUND Medical research for processing medical data is required to incorporate a governance system. Health data governance includes various elements. Among the values of governance, this study focuses on accountability and transparency. OBJECTIVE This paper proposes the system requirements for a communication platform to help medical researchers be accountable and transparent about medical data processing in medical research. METHODS We first examined accountability and transparency to find their shared bases and confirmed their importance by visiting medical research practices. Subsequently, we explored legal syllogism as the representative of rule compliance analysis to determine the system requirements to achieve the bases. RESULTS By examining accountability and transparency, we confirmed that these values were inherently vague but had two shared features– "organizing information" and "effective communication." Next, by analyzing the actual research process, we found that researchers needed to communicate effectively with legal and ethical experts to obtain appropriate support at the research planning phase. From these findings, the concept of a communication platform was derived. Through the analysis of the syllogism, we found three system requirements for the platform: (1) covering the entire chain of data processing activities; (2) being capable of recording relevant information for rule compliance analysis; and (3) being able to record compliance analysis results. CONCLUSIONS We introduced an example of a user interface in line with the discovered system requirements and discussed how our design can facilitate patients' and society's interests by empowering researchers to be accountable and transparent for their research. To support medical researchers to be accountable and transparent for their research, we proposed system requirements for a communication platform. CLINICALTRIAL N/A

Medical data security in digital transformation of healthcare: Assessment of e-Health solutions standarisation in the European Union

The paper assesses the security of medical data processing in the standardization of e-Health solutions in the European Union. First, the main cyber risks are identified, and then the effectiveness of health data protection and its interoperability between ICT systems is analysed in terms of strategy and regulatory support provided by the EU. The study indicates that the provisions of the GDPR seem to enhance processing of technological standardisation of e-Health solutions to follow the principle of technological neutrality when defining the required security measures.

Rancang Bangun Website Rekam Medis Elektronik di Fasilitas Pelayanan Kesehatan Praktik Dokter

Electronic medical records record electronic medical records which contain personal data, demographic data, social data, clinical / medical data. Processing of medical record documents at doctor's practice health facilities is still done manually, starting from patient registration, writing examination history, and storing medical record documents. One of the efforts to overcome these obstacles is by building an Electronic Medical Record website. The website development method uses the development life cycle system. Medical records are processed from input patient data, diagnostic data, action data, drug data, officer data, registration data, examination data. Then the data is processed to produce reports, including patient data, and examination data. The electronic medical record website used can simplify the processing of medical record data.