Bachelor in Healthcare Law and Compliance Management
Programme at a glance
Bachelor · 3 years · Paris College of Law and Justice
Start your applicationCompare tuition feesProgramme overview
Study legal responsibilities, data governance and compliance processes in healthcare. Medical-device and healthcare-organisation cases develop regulatory research, document review and risk analysis. Advanced study integrates regulatory strategy, technical evidence, post-market oversight, organisational governance and cross-functional compliance projects.
EDJ Paris — Paris College of Law and Justice. Duration: 3 years.
Bachelor study progresses from foundations and guided exercises to integrated applied projects.
Study pathways
Medical-device regulation; health-data governance; healthcare organisational compliance. All pathways share a common core. Indicate your preferred pathway when applying; actual availability is confirmed before admission.
Learning outcomes
- Develop healthcare law skills in institutions, products and responsibilities, explaining methods, evidence and limitations.
- Develop medical-device regulation skills in classification, obligations and documentation, explaining methods, evidence and limitations.
- Develop data protection skills in health data and access permissions, explaining methods, evidence and limitations.
- Develop quality processes skills in records, review and improvement, explaining methods, evidence and limitations.
- Develop risk management skills in complaints, incidents and communication, explaining methods, evidence and limitations.
- Develop regulatory research skills in sources, currency and reasoning, explaining methods, evidence and limitations.
Learning content and competency modules
| Module | Learning content | Assessment evidence |
|---|---|---|
| Healthcare law | Institutions, products and responsibilities | Problem definition and reasoned analysis |
| Medical-device regulation | Classification, obligations and documentation | Reproducible case or model documentation |
| Data protection | Health data and access permissions | Quality and traceability records |
| Quality processes | Records, review and improvement | Comparison of options and testing evidence |
| Risk management | Complaints, incidents and communication | Project plan and collaboration records |
| Regulatory research | Sources, currency and reasoning | Integrated report and oral defence |
Study progression
- Year 1: develop foundations, reading, analytical communication and guided cases.
- Year 2: deepen specialist methods through pathway projects and evaluation of results.
- Year 3: integrate methods in a final applied project, portfolio and oral defence.
Projects and practice
Analyse applicable requirements and documentation gaps for a medical device or healthcare organisation.
Document the problem, working process, personal contribution, validation evidence and limitations. Individual contributions are assessed within team projects. Placements and external projects depend on actual arrangements.
Teaching and assessment
Legal reading, case seminars, document exercises and professional simulations develop reasoned analysis and practical judgement. Work remains within the applicable legal system and authorised professional responsibilities.
Assignments, case or laboratory work, staged projects and the final defence assess accuracy, methods, evidence quality, practical reliability and communication. Assessment weightings, reassessment and extension rules are published before teaching begins. Moodle may support resources, assignments, quizzes and feedback; specialist practical activities are assessed separately.
Entry requirements
Provide evidence of secondary education or equivalent study. Applicants should demonstrate strong reading, writing and analytical reasoning. Mastère applicants should explain relevant legal or professional foundations. Teaching-language and legal-system requirements are stated for each programme.
Submit education evidence, transcripts, a CV, a motivation statement and any requested project materials. Teaching language, language evidence and document-translation requirements are published for the intake. Website language does not determine teaching language.
Diploma
Complete the required modules, assessments and final project to receive an institution-issued diploma.
Career development
Healthcare compliance assistant; regulatory documentation assistant; data-governance assistant. Employment depends on individual skills, experience and employer requirements. Regulated work requires the applicable qualifications and authorisations. Further study is assessed by the receiving institution.
French foundations and European perspectives
Healthcare and medical-device cases connect French responsibilities with relevant European Union regulatory frameworks, data protection and compliance evidence. Students distinguish product requirements from organisational responsibilities.
Tuition fees
| Study format | Per academic year | Full programme reference |
|---|---|---|
| Online | €3,900 | €11,700 |
| On campus | €6,900 | €20,700 |
Fees are charged per academic year. The full-programme reference assumes the same annual rate throughout the programme.
Apply to this programme
Start your applicationEntry requirements and admissionsCompare all law programmesExplore legal education with French foundations and a European perspective at
EDJ Paris, a law school in Paris