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Gesundheitsrecht

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Overview

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Learning outcomes

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Course content

1

Einführung In Das Gesundheitsrecht

2

Patientenrechte Und Aufklärungspflicht

3

Arzneimittelgesetz Und Zulassung

4

Krankenhausfinanzierung Und -Organisation

5

Datenschutz Im Gesundheitswesen

Career Path

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Key facts

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Why this course

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People also ask

Everything you need to know before you start

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We offer immediate access to our course materials through our open enrollment system. This means:

  • The course starts as soon as you pay the course fee, instantly
  • No waiting periods or fixed start dates
  • Instant access to all course materials upon payment
  • Flexibility to begin at your convenience

This self-paced approach allows you to begin your professional development journey immediately, fitting your learning around your existing commitments.

We offer two flexible learning paths to suit your schedule:

  • Fast Track: Complete in 1 month with 3-4 hours of study per week
  • Standard Mode: Complete in 2 months with 2-3 hours of study per week

You can progress at your own pace and access the materials 24/7.

There are no formal entry requirements for this course. You just need:

  • A good command of English language
  • Access to a computer/laptop with internet
  • Basic computer skills
  • Dedication to complete the course
Ready when you are
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Assessment is done through:

  • Multiple-choice questions at the end of each unit
  • You need to score at least 60% to pass each unit
  • You can retake quizzes if needed
  • All assessments are online

Upon successful completion, you will receive:

  • A digital certificate from London School of Business and Administration
  • Option to request a physical certificate
  • Transcript of completed units
  • Certification is included in the course fee
Open enrolment · Start today

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Why people choose us for their career

Trusted by professionals worldwide

Verified outcomes from learners who finished the course and put it to work.

4.5
Based on 4 learner reviews · 4 countries
98%
Would recommend
100%
Verified learners
2026
Cohort active
Completed from United States
MC
Michael Carter
US · Course completed

The Gesundheitsrecht course at Stanmore School of Business was exactly what I needed to meet my learning objectives in health‑care compliance. The modules on patient consent and liability gave me concrete frameworks that I applied directly to a compliance audit for my employer. The case studies were current and the reading pack included the latest federal statutes, which made the material feel highly relevant. Overall, the instructional quality was top‑notch and I feel fully prepared to advise on legal matters in a clinical setting.

SL
Sophie Laurent
CA · Course completed

I took the Gesundheitsrecht class because I wanted a solid grasp of health‑law basics before starting my job at a hospital. The course was surprisingly laid‑back yet packed with useful info – I learned how to draft proper consent forms and got a clear rundown of privacy rules that I could actually use the next day. The video lectures were clear and the downloadable PDFs were easy to reference. It wasn’t perfect, but it definitely helped me hit my learning goals and feel more confident on the job.

FW
Felix Wagner
DE · Course completed

Wow – the Gesundheitsrecht program blew me away! The enthusiastic teaching style kept me engaged, and the role‑play simulations on GDPR‑compliant patient data handling were priceless. I walked away with practical skills like conducting a legal risk assessment for tele‑medicine services, which I’ve already applied during my internship at a biotech startup. The course materials were up‑to‑date, with real‑world examples from both the EU and the US, making the content incredibly relevant. I’m thrilled with the experience and would recommend it to anyone looking to specialize in health law.

HT
Haruki Tanaka
JP · Course completed

The Gesundheitsrecht course offered by Stanmore School of Business provided a highly detailed overview of international health‑law regulations. I appreciated the thorough analysis of cross‑border medical device approvals and the step‑by‑step guide to performing regulatory impact assessments. The slide decks were rich with charts and the supplementary readings included recent case law from both Europe and Asia, which helped me understand the practical implications for my work at a pharmaceutical company. Overall, the learning experience was rigorous and met my expectations for depth and applicability.

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Skills gained

Legal Analysis
Regulatory Compliance
Risk Management
Patient Advocacy
These skills will be developed throughout the course


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Taught in English

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Recently updated!

May 2026