Bioglan AB is a contract development and manufacturing organization with more than thirty years of experience in research, development, manufacturing and marketing of pharmaceuticals. 

We develop, produce and market pharmaceuticals and medical devices. We also provide support for pharmaceutical, healthcare and life science companies in all aspects of development and manufacturing of semi-solid and liquid products. We collaborate with companies of all sizes, from the smallest start-up to the leading pharmaceutical companies. 

Our manufacturing authorization from the Swedish Medical Products Agency allows us to produce non-sterile semi-solid and liquid products, both at pilot scale for clinical trials or at full-scale to supply a large commercial market. We can even be your QP release site for other types of products. Our quality system fulfils the EU and FDA GMP (Good Manufacturing Practice) requirements as well as the ISO 13485 standard for Medical Devices. 

Bioglan is a reliable, efficient and flexible organization that delivers projects with the best quality at the right time in a cost-effective way. We are proud that we meet the quality requirements of the global markets.

Manufacturing

Pharmaceutical

Bioglan AB

Bioglan AB's headquarters in Malmö, Sweden

This department ensures that products meet established quality standards through systematic testing and analysis.

Quality Control

This department ensures compliance with regulatory standards and oversees quality control processes within the organization.

Quality Assurance

This department focuses on managing and developing products to meet market needs and support sales initiatives.

Product Development

This department manages and oversees production processes and machine operations to ensure efficient manufacturing.

Production Operations

This department manages and facilitates quality control processes to ensure the integrity and success of projects and laboratory operations.

Quality Control Support

This department manages compliance with regulations and oversees the submission of necessary documentation to ensure product safety and efficacy.

People (9)

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Other teams

Quality Assurance

Product Development

Production Operations

Quality Control Support

Regulatory Affairs