Elomatic Life Science provides a full range of engineering and technical consulting services for the Biotech and Pharmaceutical industries from feasibility studies to design, commissioning, start-up and validation.

Elomatic follows the cGMP in the facility design and has extensive knowledge in GAMP and 21CFR Part 11.

Elomatic has adopted Good Engineering Practices that ensure time and cost saving design, commissioning, qualification and validation of new and existing process facilities. With our in-house document management system, EloDoc, we are able to establish and maintain project documentation that is valid throughout the project. This project documentation forms the backbone of the successful life cycle management of the plant or its separate parts.

The proof of our know-how and experience in Bio and Pharma are the several facilities that have been approved by EMEA and FDA.