Get medical developments ready for series production efficiently, in compliance with the law and quickly

With MDR to more efficient processes in production and supply chain.

Get medical developments ready for series production efficiently, in compliance with the law and quickly

With MDR to more efficient processes in production and supply chain.

What challenges do you face when developing product innovations?


Are you spending more and more money on normative requirements?


Are you lacking a strategy to name and prioritize challenges?


You want employees who know and can implement the MDR requirements?


Does MDR also increasingly prevent you from listening to your customers? You only hear what you are obligated to do because of MDR?


You and your suppliers no longer know how to implement the additional requirements?


Your employees seem to be working on the wrong issues or your employees are not aware of the “new” requirements?

At 3R LifeScience, we ensure that you can implement your product ideas efficiently and in compliance with the law, despite increasing complexity in product development.

Lieferantenmanagement mit Erfolg


You don’t like to have new surprises after the development is finished – plan your design transfer at least as much as your development.


You have a roadmap of how and where to develop your suppliers for an efficient and cost-reducing supplier-customer relationship.


The requirements are documented in writing, known and comprehensible with regard to the products, suppliers and processes.


Risk management, that also works very well in production and supplier management. With the right strategy, you focus on the most important tasks, not the most urgent ones.


They create a basis for building long-term, trusting cooperation with mutual support in difficult situations.


Abweichungen fallen schnell auf, weil Sie im Prozess arbeiten und Sie sich regelmäßig selbst prüfen.

Use the knowledge advantage of experienced medical devices project managers for progress and growth.

From possibility to reality

From requirements management to the development of feasibility studies, functional samples and prototypes to verification, validation, approval and market launch – our specialized project managers are at your disposal for any project phase.

Research & Product Development

Supply Chain & Production


Quality Management & Regulatory

Business Development

These companies ensured their successful future in the MedTech world through our cooperation:

Pulsion Logo
Berlin Heart Logo
Life Systems Logo
Getinge Logo

Case Studies

Project management development of a class IIb/ III product

The company: Internationally active medical technology company in the field of orthopedic implants and instruments.

The task: Review and set-up of processes for CE marking and product registration of medical devices.

Our work: We evaluated the status quo of processes for CE marking and product registration of class I, IIa, and IIb medical devices and implemented additional processes to ensure that regulatory requirements for conformity assessment of both national and international registrations are met. This involved optimizing Regulatory Affairs’ interfaces with other departments and taking steps to integrate the new processes and structures into the company’s quality management system.

Customer benefits: Targeted measures created structures and processes that enabled our customer to optimize its internal processes for CE marking and improve communication with Notified Bodies and national registration authorities. The sustainability of our measures was confirmed in audits.

Product portfolio recertification and MDR gap analysis

The company: Internationally active medical technology company with resorbable bone substitute materials.

The task: Planning and execution of the recertification of the product portfolio according to the European Directive as well as gap analysis regarding MDR requirements.

Our work: We reviewed the technical documentation for the Class III product portfolio and created a new design dossier as part of the recertification. The new MDR requirements and requirements from technical standards were defined and implemented in consultation with the Notified Body.

The customer benefit: Our client’s product portfolio was recertified on time and within budget. New regulated requirements were reviewed and comprehensive remediation measures were initiated to further improve the documentation of the established product portfolio.

“When words were followed by actions and actions by results, I was more than convinced! Thanks to 3R LifeScience, we were able to successfully complete more than a singular product development and bring a product to market that has a great impact for our patients.

In addition, we were able to do a great deal of groundwork of an organizational nature within the company, from which we will benefit in the long term.”

Sven-René Friedel
General Manager,
Berlin Heart GmbH

“We understand that the MDR changes a lot of things for you and raises a lot of questions.”

Together with one of our experts, you clarify your requirements and questions. If cooperation is possible, we will arrange a workshop with you.

If you already have clarity about your project requirements and now need support as soon as possible, do not hesitate to call us.

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