Your Trusted Partner in Every Step of the Development and Production of Medical Devices
Did you know that Teampac can be a legal manufacturer and take full responsibility for the conformity of your products?
We recognize that taking a medical device from concept to shelf is a process that requires meticulous work and expertise, but you can rest easy, as we will guide you through the entire journey and support you with all the product documentation requirements.
When selling medical devices in the EU, obtaining the CE marking is essential. The CE marking indicates that the medical device:
- meets safety and performance requirements (GSPR)
- complies with relevant product standards
- has been evaluated against the requirements.
Teampac can be a legal manufacturer and take full responsibility for the medical device’s design, development, production, packaging, and labeling. Our professionals will be there to help and support you at every stage. A legal manufacturer confirms that medical devices are produced and brought to market in compliance with applicable laws, standards, and regulations. The goal is to ensure that medical devices are safe, effective, and meet quality standards. As a legal manufacturer, Teampac is also responsible for that your product achieves CE marking.
With us, you can rest assured that the medical devices have been thoroughly tested and their documentation is in order.
Teampac – Proud Part of Your Brand
