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Products
taube-med gets you audit-ready fast.
Built for software innovators who want to launch without the regulatory headache.
Regulatory Consultancy
Regulatory expertise for MDR.<br />Strategic guidance and hands-on support to resolve compliance challenges efficiently.
QMS Smart Start
A modular QMS system. <br> Includes pre-validated templates and AI-supported workflows to streamline implementation and ensure audit readiness.
TD Made Easy
Automated technical documentation aligned with MDR. <br>Structured input prompts and real-time logic checks ensure completeness, consistency, and traceability.
Features
Our Featuress
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Project
Our Projects
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Team
Our Team
We give you the tools, guidance, and confidence to manage regulatory tasks yourself — with our support whenever you need it.
Astrid Schulze is a regulatory expert with 30+ years of experience in MedTech certification. At taube_med, she simplifies compliance for startups and SMEs.
Ella Kadas is a computer scientist and entrepreneur focused on AI in medical imaging. At taube_med, she shapes the product strategy to empower innovation.
OUR SERVICES
What We Provide
On-Demand Consultancy
Book expert sessions with Astrid to solve specific regulatory challenges fast.
01
Setup & Onboarding Support
We help you get started with your documentation tools and make sure everything fits your setup.
02
Review & Feedback
We’re with you all the way — reviewing each step so your documents are solid and audit-ready.
03
A Community of Innovators
A space to exchange ideas and help shape the future of compliance tools — together.
04
Flexible Packages
Use only what you need — no one-size-fits-all, just practical, tailored support.
05
PRICING PACKAGES
Choose Your Best Plan
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Testimonial
Our Client’s Reviews
Dr. Andreas Sprock
We worked with Astrid Schulze on setting up our QMS and placing our first medical device on the market. Her strategic expertise and structured approach to complex regulatory issues in the field of medical software were of great value to us. Astrid has always succeeded very well in showing the big picture and thus communicating even complicated topics in an understandable way. I am pleased to be able to recommend Astrid to others.
We worked with Astrid Schulze on setting up our QMS and placing our first medical device on the market. Her strategic expertise and structured approach to complex regulatory issues in the field of medical software were of great value to us. Astrid has always succeeded very well in showing the big picture and thus communicating even complicated topics in an understandable way. I am pleased to be able to recommend Astrid to others.
Sunil Yadav
“Working with Astrid Schulze has always been a real support. She makes complex regulations clear and always adapts them to the realities of small companies. It’s rare to find someone who combines deep expertise with such practical thinking.”
Sven Büttner, Vivira
Astrid is a competent partner for all things Quality Management and Regulatory Affairs. I have come to appreciate working with her in the field of medical software and digital health applications (DiGA). Her calm and focussed manner plays a key role in ensuring that even critical projects (e.g. inspections by the competent authority) are completed on time and without any complaints. Her holistic perspective ensures that people are not lost sight of, even under pressure to perform. Whether technical documentation, clinical evaluation or QM system: Astrid is the right person for the job.
Astrid is a competent partner for all things Quality Management and Regulatory Affairs. I have come to appreciate working with her in the field of medical software and digital health applications (DiGA). Her calm and focussed manner plays a key role in ensuring that even critical projects (e.g. inspections by the competent authority) are completed on time and without any complaints. Her holistic perspective ensures that people are not lost sight of, even under pressure to perform. Whether technical documentation, clinical evaluation or QM system: Astrid is the right person for the job.
Karl-Heinz Sicklinger
Astrid Schulze was very helpful in developing a regulatory strategy for our medical devices. By registering our products in a medical system, we were able to save a lot of time and money. Thanks to her project management, we were able to successfully complete the approval process within our time and budget.
Astrid Schulze was very helpful in developing a regulatory strategy for our medical devices. By registering our products in a medical system, we were able to save a lot of time and money. Thanks to her project management, we were able to successfully complete the approval process within our time and budget.
Our Blog
Our Blog
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WHY CHOOSE US
Creating A Community Of Life Long Learners.
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185+
Learners & counting300+
Courses & Video500+
Certified Students49+
Registered Enrolls
Work Process
A wide range of processs
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01
Waste pickup
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Waste collection
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Proccessing
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Recycling
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Timeline
We have experienced many landmark Moments.
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2013
February
This year has seen the biggest upgrade in UK.
2014
March
This year has seen the biggest upgrade in UK.
2015
April
This year has seen the biggest upgrade in UK.
2016
May
This year has seen the biggest upgrade in UK.
2017
June
This year has seen the biggest upgrade in UK.
2018
July
This year has seen the biggest upgrade in UK.
2019
Agust
This year has seen the biggest upgrade in UK.
About Our Conpany
Choose Reviews IT Service Company
An IT firm or MSP who keeps your IT running smoothly at all times is like a plumber who fixes your pipes; that’s what they are supposed to do. Many IT firms struggle.
Countdown
Please Wait We Provide
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OUR GALLERY
What We Provide
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Product
Our Products
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