We are a Contract Development and Manufacturing Organisation (CDMO) focused on regenerative medicine. Our company addresses product/process development and current Good Manufacturing Practice (cGMP) production and clinical translation of impactful medicinal products. Stemmatters´ core expertise addresses multiple investigational medicinal products (IMPs), including advanced therapy medicinal products (ATMPs), biologicals, and diverse raw materials supporting the product life cycle of innovative therapeutic products.

Stemmatters

This department focuses on scientific research and the development of new products and technologies.

Research and Development

This department oversees and manages the processes involved in the production and assembly of goods.

Manufacturing Operations

This department ensures that products meet quality standards and specifications through rigorous testing and assessment.

Quality Control

This department provides strategic guidance and expertise to support organizational goals and initiatives.

Advisory Board

This department focuses on identifying growth opportunities and building relationships to drive the company's expansion.

Business Development

This department manages financial reporting, regulatory compliance, and quality assurance in processes.

Stemmatters

Org chart

Teams

Research and Development

Manufacturing Operations

Quality Control

Advisory Board

Business Development

Finance and Compliance

Offices

Stemmatters

Org chart

Teams

Research and Development

Manufacturing Operations

Quality Control

Advisory Board

Business Development

Finance and Compliance

Offices

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