Services

Every simulation brings you closer to patient protection

Partnering in the Preclinical evaluation of Medical Devices

In our testing laboratory, ideas evolve into safe medical products. Applications are simulated within a controlled environment and refined through confidential collaboration between users and developers. 
This approach ensures that potential issues are identified and addressed early, preventing malfunctions or misuse that could compromise patient safety.
Here, you will collaborate with renowned physicians who are dedicated to advancing safe medical devices by sharing their expertise and insights.

Preclinical evaluation of medical devices - Your partner for success

Initial Contact & Needs Assessment

Everything begins with a personal discussion about your planned medical device. Together, we define the project scope, clarify requirements and expectations, and decide whether an animal model or human tissue sample is best suited for your preclinical tests.

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Step

Customized Proposal Development

Based on your specific needs, we develop tailored solutions:

  • Study Planning Consultation: Strategic support for a solid foundation.
  • Application Support: Expert assistance in handling regulatory approvals for animal testing.
  • Preclinical Evaluation Execution: A comprehensive solution for your testing needs.

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Step

Contract Signing

Once all the details have been clarified and the final agreement on the offer has been reached, the contract is signed. This forms the basis for the subsequent project steps and formally secures the collaboration.

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Project Start & Excecution

Application Submission (if animal testing is required)
Kick-off Meeting: Planning the next steps.
Joint Application Submission: Efficient cooperation with regulatory authorities.
Approval: The green light to begin after receiving regulatory approval.
Preclinical Testing Execution
While you conduct the tests, we provide full support:

  • Modern Infrastructure: Provision of facilities and medical technology.
  • Expert Assistance: OR support and medical consultants as needed.
  • Comprehensive Care: Ensuring animal welfare when using animal models.
  • Quality Control: Regular reviews to ensure smooth operations.
    Results Delivery and Completion
  • Detailed Documentation: Full documentation for your next steps.
  • Feedback Session: Joint evaluation to optimize our collaboration. 

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Follow-up Support

MiG remains the customer’s point of contact even after the project has been completed. Our team will respond quickly and competently to any follow-up questions or support requirements.

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Contact us today to learn more and take the next step in your medical device journey

User Training

Medical User Trainings for patient safety and legal conformity

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Enhancing Patient Safety Through Comprehensive Medical Device User Training

Understanding the functionality, limitations, and potential hazards of the equipment ensures that users can make informed decisions during critical moments.

MIG significantly contributes to this by offering specialized, hands-on training programs in a serene environment, away from the pressures of clinical settings.

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This approach allows participants to fully immerse themselves in learning, gaining practical experience with medical devices in a controlled and supportive atmosphere.

By combining expert instruction with real-world scenarios, MiG ensures that healthcare professionals are well-prepared to use these devices safely and effectively, ultimately enhancing patient safety.

The full value of medical learning comes from practical experience. It is only through experience that knowledge becomes expertise.

Initial Contact & Needs Assessment

The first step is to clarify your objectives and requirements for the planned training. Whether it is individual training or comprehensive training for entire teams, we will help you find the right training approach. We also look at regulatory requirements, such as animal testing approvals

01

Step

Customized Proposal Development

On the basis of your specifications, we will develop a tailor-made offer that covers both the scope and the practical feasibility of your project.

02

Step

Contract Signing

Once all the details have been clarified and the final agreement on the offer has been reached, the contract is signed. This forms the basis for the subsequent project steps and formally secures the collaboration.

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Step

Project initiation and implementation

Planning and Organization
Our project managers provide optional organizational support, such as hotel and transfer bookings, and prepare all the details for the event.

Delivering the training
On the day of the training, everything starts with a short introduction, followed by the practical implementation:

  • Facilities and medical equipment: we provide you with state-of-the-art equipment.
  • Specialist support: Assistance in the operating theatre and supervision of patient replacement models
  • Experienced trainers: Experienced trainers available on request.
  • Quality assurance: Regular checks to ensure everything is running smoothly.

 

Conclusion
Upon completion, the project is evaluated both internally and externally

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Follow-up Support

MiG remains your contact and continues to provide support after the project ends. Images created on behalf of the client are delivered..

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Take the next step on your way to safe medical devices!