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Quality & Regulatory

Morphoplant is a dedicated business focused on serving all the requirements of the biotechnology and related industries. Morphoplant is devoted to offer worldwide academic and industrial collaborators in the fields of biomaterials research first class products and services. Our regulatory and quality assurance team is therefore committed to continuous quality control of all products and services. In order to continuously improve and refine our products and services we strongly encourage customer feedback. Addressing academic and industry challenges will finally improve the quality of life for patients.


Morphoplant's development process is certified in accordance with DIN EN ISO 13485 (Medical devices - Quality management systems  - Requirements for regulatory purposes). ISO 13485 as an internationally recognized quality standard requires an organization to demonstrate that it has the comprehensive quality management systems in place to consistently meet the specific customer and regulatory requirements applicable to medical equipment.

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