Our vision for the Life Sciences Industry

Our approach begins with regulatory compliance, followed by process improvement, using quality by design principles.

A different approach, incorporating QbD with a focus on regulatory compliance and efficiency optimization

We care as much as you do about improving patient safety and process sustainability, which motivates us to help record contextualized data and control processes, in accordance with regulations.

With over 50 years of experience in life sciences, we understand the challenges of working within a regulatory framework and the importance of a modular, science-based approach.

Focused on key applications and following the principles of Quality by Design (QbD), we continue to invest in the development of digital engineering solutions (DES) to help reduce project delivery costs, risks and time to market, as well as offer services that help reduce operating costs.

Sustainability is part of our culture, so our solutions are designed with this in mind, to help eliminate process waste and meet your emissions reduction goals.

Discover key updates to EudraLex GMP, Annex 1 >

Discover key updates to ISPE GAMP 5 Second Edition >

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Laboratories and R&D plants

We know that developing compatible processes to make pioneering medicines and combat new diseases is expensive and time-consuming.

That’s why we incorporate quality by design in pharmaceutical development in our process development phases. Through modular Plug-and-Produce solutions, we help bring together contextualized data to generate exception (non-compliance) reports and provide “prior knowledge” to feed lab, plant and enterprise dashboards.

API Greenfield Facilities (Large and Small Molecules)

For those responsible for the quality and efficiency of GMP-compliant plants, staying up-to-date and applying regulations is often overwhelming.

Our digital engineering solutions follow the quality life cycle suggested by ICH Q8: Identify Critical Process Parameters, Risk Management, Good Engineering Practices (GEP) and Qualification. Documentation can be provided in a paperless format through a SaaS platform.

Brownfield API Facilities (Large and Small Molecules)

Existing manufacturing plants need to implement continuous improvements to remain competitive, but we recognize that this can be difficult in validated environments.

Our expertise in how to address validation constraints and manage changes with minimal impact is helping companies achieve their desired process efficiencies and eliminate segregated (siloed) data collection.

Complete and finish (secondary pharmaceuticals)

The trend of putting the patient at the center involves the production of personalized medicines, but following this path requires a complete transformation of manufacturing principles.

We closely follow life science trends to enable customers to quickly adapt to innovative concepts, for example: modular processing, single-use systems, continuous versus batch processes, cold chain management, etc. Our technology offers easy connectivity at the edge, helping to create decentralized and interoperable systems.

Services

Consumers raise questions about the use of resources and energy, and the generation of waste and emissions, how can you improve sustainability and your carbon footprint?

Eurotherm is committed to empowering everyone to make the most of our energy and resources. We apply GEP and help comply with GMP, but our digital engineering solutions prioritize reducing environmental impact over the profitability of project execution.