Shelf Life and Transport­ation Validation of Medical Devices

Two colleagues sit in an office with plants in the background, talking to each other.

Quickly and without unnecessary effort to a compliant durability proof of your medical device

Regulatory Safety

Our experts come from testing laboratories and manufacturers. They are familiar with the re­quire­ments of the notified bodies and know exactly what is needed for a successful approval.

Efficiency through Expertise

We use existing data and combine different tests where possible. That saves time and money without compromising on quality.

Single Source

Our more than 100 experts can also help you with other aspects, such as biocompatibility or electrical safety, and ensure that your docu­mentation is consistent and coordinated.

Fast Market Launch

With short response times and efficient proce­sses, we help you bring your devices to market faster, giving you a competitive advantage.

Global Competence

Our testing and documentation fulfill the requirements of all relevant markets, saving
​​​​​​​you the need for costly multiple tests.

Pragmatic Approach

We focus on the essentials and avoid unneces­sary effort – without any compromises regar­ding conformity.

Standard-compliant shelf-life testing and transportation validation: We ensure a smooth approval of your medical device

Lack of clarity regarding regulatory require­ments, uncertainty about the scope of testing, and fear of making mistakes when conducting shelf-life tests and validating transpor­tation can lead to costly delays or even product recalls.
Without professional support, you risk not only the market launch of your medical device but also your reputation.

Our experts support you every step of the way – from planning to documentation

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Strategic Consulting

Our team of experts develops customized testing strategies, defines optimal test para­meters, and evaluates both material and packaging to plan your shelf-life tests perfectly.

Project Management

If desired, we can take over the complete project planning and mana­gement for valida­ting the shelf life of your medical devices in close cooperation with external laboratories and your team.

Gap Analyses

Our experts review your documentation to validate the shelf life and identify gaps to ensure compliance with all regulatory requirements.

Quality Assurance

To ensure consistent and complete docu­men­tation, we integrate all relevant aspects, such as biocompatibility, electrical safety, and risk management.

Mann und Frau prüfen ein Dokument

Contact us​​​​​​​ now to develop the optimal strategy for proving the durability of your medical devices.

Get in touch, we're happy to help!
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+1 (240) 638 27 09

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Further support for the safety of your medical devices

Biocompatibility

Our expert team helps you create a comp­lete and legally compliant bio­com­pa­tibility file.

 

Electrical Safety

With our support, you receive compliant documentation to prove electrical safety
​​​​​​​or electromagnetic compatibility.

Risk Management

We help you quickly pass approvals, audits, and reviews with legally compliant risk management files and safe devices.

 

E-Learning, Seminars, Workshops

Want to gain more knowledge? Our custo­mized e-learning courses, seminars, and workshops put you on equal footing with experts.

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