Practice Areas

Digital Healthcare

2025.12.11

Digital healthcare is a field that demands both technological innovation and careful management of legal risk as advanced technology and a fast moving regulatory environment continue to develop.

1. Digital Healthcare | Concept

Daeryun practice area, concept of digital healthcare

Digital healthcare is a next-generation industry that builds on advances in IT technologies such as artificial intelligence, big data, and cloud computing to drive the digital transformation of medical services as a whole.

By analyzing patient-generated health data (PGHD) gathered through sensors, wearable devices, and various platforms, it delivers personalized health management and disease prevention services that extend the reach of conventional medical care.

As low birth rates, an aging population, and the rise in chronic disease make health management more important, public interest in and demand for digital healthcare are also growing quickly.

In response to that demand, a range of industries, including pharmaceutical companies, IT companies, and the financial sector, are entering the market in earnest.

A National Strategic Industry

Digital healthcare is a field the government has designated as a future national strategic industry, and it is building out an institutional and policy foundation for the field in a systematic way.

As the national goals of improving the quality of medical services, lowering costs, and responding to demographic change converge with technological innovation, the field's industrial significance is widening, while interest in personal health management and demand for data-driven personalized care raise the market's growth potential further.

Against this backdrop, domestic and foreign companies are competing to enter the market, establishing digital healthcare as a core next-generation industry.

2. Digital Healthcare | Types

types of digital healthcare, practice area

Digital healthcare is an industry where technology and medicine come together to enable personalized health management and prevention, and it generally falls into four broad areas.

Mobile Healthcare

Mobile healthcare uses smartphone applications and wearable devices to support health management in everyday life.

Well-known wearable devices such as the Apple Watch and the Galaxy Watch measure a range of biometric data, including heart rate, activity levels, and sleep duration, and they suggest exercise and sleep routines tailored to an individual's lifestyle.

Moving beyond their early activity-tracking functions, newer devices can measure varied physiological data such as electrocardiogram readings, body temperature, blood glucose, and oxygen saturation, which makes more personalized health management possible.

A variety of mobile healthcare services are also available, including chronic disease management, medication reminders, and apps that offer support by stage of pregnancy, so that data-driven personalized management combining wearables and apps is becoming part of daily life.

Telemedicine

Telemedicine is a remote medical service in which clinicians and patients consult and provide treatment through voice or video systems rather than meeting in person.

As a broad concept, telemedicine covers both remote treatment and remote patient monitoring. Remote monitoring gives patients a way to have their health status checked and to receive further intervention when needed, without traveling to a hospital.

Telemedicine can allow information to be exchanged quickly without an in-person visit, and it can ease the burden of traveling to a hospital.

Smooth operation, however, generally requires accurate sensors, reliable data transmission systems, integration with electronic health records (EHR), and supporting telemedicine infrastructure.

Health and Medical Analytics

Health and medical analytics collects and analyzes an individual's precision medical data to identify the causes of severe and intractable diseases and to offer tailored treatment options.

With recent advances in artificial intelligence and big data technology, analysis that draws on genetic information has also become possible, which can support medical care optimized for each individual.

For accurate analysis and the safe use of data, the systems for collecting, managing, and securing medical data must be maintained rigorously.

Digital Health and Medical System

A digital health and medical system digitizes personal health records so that medical institutions and patients can share information and communicate in a systematic way.

As a core foundation for digital healthcare services, it enables data-driven personalized management and the efficient delivery of medical care.

For such efficient operation, the systems for data transmission, record management, and personal information protection must be fully in place.

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3. Digital Healthcare | Digital Medical Devices

Within digital healthcare, digital medical devices are software and hardware products designed on the basis of clinical evidence to prevent, manage, and treat disease.

Unlike conventional wellness devices or simple health-management devices, these products generally presuppose a physician's prescription and ongoing monitoring of the patient's condition, and their safety and efficacy must be verified.

Digital therapeutics, in particular, work to improve the quality of life of patients affected by disease or treatment on the basis of clinical evidence, and security and the protection of personal information are also considered when patient data is stored and shared.

Domestic Regulatory Trends

For digital medical devices, the regulatory framework is being built out gradually in step with the government's strategy of fostering the industry, and its main features are as follows.

▶ Legal Basis and Support Policies

Through the Act on the Promotion of and Support for the Medical Device Industry and Innovative Medical Devices, the Korean government has introduced mechanisms for rapid market entry, such as the designation of innovative medical devices and special exceptions for SaMD certification.

Companies whose products are designated as innovative medical devices may receive benefits such as exemption from submitting certain technical materials and a simplified integrated review.

▶ Use of Data and Application of AI

With the enforcement of the Three Data Acts (the Personal Information Protection Act, the Network Act, and the Credit Information Use and Protection Act), the use of personal information and pseudonymized information has become possible, broadening data access for the development of AI-based diagnosis and treatment solutions.

The Ministry of Food and Drug Safety has also issued guidelines for the approval and review of digital therapeutics, clarifying the makeup of technical documents, clinical evidence requirements, change-approval standards, and related matters.

▶ Clinical Trials and Development Efficiency

Under the clinical trial management standards revised in 2023, clinical trials can be conducted remotely even when clinicians and patients do not come into direct contact.

This allows developers to verify the safety and efficacy of digital medical devices more efficiently and quickly.

A regulatory environment of this kind strengthens the foundation for growth in the digital healthcare industry and plays an important part in building global competitiveness on the basis of ICT capabilities and digital infrastructure.

Within this framework of policy support and regulation, digital medical devices can deliver patient-tailored medical services while also driving industrial innovation.

Regulatory Sandbox and Legislation

To bring digital healthcare into commercial use quickly, related legislation and a regulatory sandbox system are being pursued.

The National Assembly has introduced the Act on Support for Digital Healthcare and the Use of Health and Medical Information, which sets out the scope for using digital healthcare and health and medical information and defines the State's policy responsibilities and support framework.

Under this bill, new digital healthcare products and services have their safety and effectiveness verified through pilot projects, and for fields tied directly to people's lives and health, a separate, specialized sandbox system applies, which allows regulatory compliance to be handled more flexibly.

By standardizing electronic health record (EHR) systems and certification procedures, designating specialized institutions to manage personal health and medical information, and establishing a system for the right to request data transmission, the bill can reinforce the foundation of the digital healthcare ecosystem and, at the same time, set up frameworks for research and development, industry, and export support.

A legal and institutional foundation of this kind can support both the safety and the rapid commercialization of digital medical devices while playing a central role in expanding access to data-driven personalized medical services.

4. Digital Healthcare | Issues in Personal Information Protection

digital healthcare, issues in personal information protection, practice area

For personalized health management and disease prevention, digital healthcare necessarily depends on the use of personal health data.

Health information, however, is classified as sensitive information under the Personal Information Protection Act, and its use can give rise to various legal and ethical controversies.

▶ Sensitive Health Data and the Limits of Consent

Data can be used on the basis of individual consent, but where it affects an entire family, as with genetic disease information, individual consent alone may not offer adequate protection.

▶ Legal Definitions and Institutional Ambiguity

The current Personal Information Protection Act does not clearly define de-identification, anonymization, or the scope of personal information, which creates confusion about how data may be used in digital healthcare.

Some information is hard to attribute to an individual on its own, yet it may become identifiable when combined with other data.

▶ The Need for Secure Data Management

For data to be used safely in digital healthcare, accurate sensors, sound data transmission and record management, and a security framework are required.

In research or industrial use, approval by an institutional review board (IRB) under the Bioethics and Safety Act can help prevent misuse.

▶ Balancing Use and Protection

Health data is central to the development of digital healthcare and the delivery of personalized medical services.

For that reason, rather than aiming for 100 percent anonymization, the better approach generally strikes a reasonable balance between usable information and the protection of personal information.

5. Digital Healthcare | Points of Caution

The digital healthcare industry holds significant potential for innovation, yet it also carries regulation, constraints, and legal risk.

1) Constraints on Data Collection and Integration

Delivering personalized services calls for collecting various lifestyle and medical data, but the Personal Information Protection Act makes it difficult to integrate or share data among private companies.

Because securing enough data is hard, analysis and the advancement of services may face constraints.

2) Low Revisit Rate

Digital healthcare services tend to be used only when needed, so the regular usage rate is low.

Because sustained participation and data accumulation are difficult, verifying and improving the effectiveness of a service can be constrained.

3) Constraints on Approval and Insurance Reimbursement

Market entry requires approval by the health and medical research institute and an evaluation of the health insurance reimbursement rate.

Steps such as health technology assessment, on-site demonstration testing, and cost-effectiveness verification can make the product launch process lengthy.

4) Various Regulations

Some services, such as telemedicine and medication delivery, are restricted domestically, and commercialization is difficult without regulatory compliance.

Because of the regulatory environment, building a track record of service use is hard, which may also hinder overseas expansion.

Digital healthcare services call for more than technical capability; they also require a sound understanding of law and regulation and the ability to manage data.

Securing enough data, the approval process, and regulatory compliance should be managed strategically so that services can run safely and sustainably.

If You Need Legal Advice

The firm's Medical, Bio, and Healthcare Group provides focused legal services that help companies manage the complex regulatory environment and legal risks they may face in a strategic way.

▷ Licensing and approval for digital medical devices, drug price listing, and new health technology assessment

▷ Filing on behalf of clients for FDA Class I, II, III and European CE/MDR approvals

▷ Legal advisory for healthcare services based on artificial intelligence (AI) and the Internet of Things (IoT) (regulatory compliance, licensing, personal information protection, and security)

▷ Telemedicine, mobile health services, and data utilization (health and medical data, big data)

▷ Review of and response to legal issues related to platform development

▷ Support for regulatory sandbox applications and approvals for the introduction of innovative technologies

Building on these services, the firm offers tailored advisory that addresses not only personal information protection and AI-related regulation but also the various rules that arise from new technologies such as digital healthcare, advanced biopharmaceuticals, and remote care.

In doing so, attorneys who focus on medical matters help healthcare companies reduce the legal risks they may face and steadily pursue the adoption of new technologies and the shift to innovative business models.

If you need legal advice on digital healthcare, you may request guidance at any time from 🔗an attorney who focuses on medical matters.