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.
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:
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Step
Contract Signing
03
Step
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:
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Step
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
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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.
Initial Contact & Needs Assessment
01
Step
Customized Proposal Development
02
Step
Contract Signing
03
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:
Conclusion
Upon completion, the project is evaluated both internally and externally
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Step
Follow-up Support
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Step
Take the next step on your way to safe medical devices!
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