Elmea
Elmea Consulting is a Brussels-based life sciences consulting firm founded in 2018. The firm provides consulting services across pharmaceuticals, biotechnology, and medical devices, with a team of consultants and freelance specialists. Core activities include quality and regulatory support, project and program management, process and manufacturing performance, IT/CSV and automation engineering, and medical/technical writing. The firm reports over 15 consultants and freelance employees in 2025.
Industries
Nr. of Employees
small (1-50)
Services
Consulting services supporting operational QA, project quality, quality control, QMS performance, audits/inspection readiness, data integrity, and HSE/ISO certification support.
Services covering technical project management, global project/program management, PMO and project cost control, agility management, and IT structuration support.
Support for process improvement, process ownership, reliability in process management, maintenance optimization, and upstream/downstream process development for biologics and gene therapies.
Software engineering and automation engineering services including CSV support, automation testing, supervision system migration and technical support for instrumentation and metrology.
Medical writing for clinical development documents and technical writing for device documentation, installation and service procedures.
Consulting services supporting operational QA, project quality, quality control, QMS performance, audits/inspection readiness, data integrity, and HSE/ISO certification support.
Services covering technical project management, global project/program management, PMO and project cost control, agility management, and IT structuration support.
Support for process improvement, process ownership, reliability in process management, maintenance optimization, and upstream/downstream process development for biologics and gene therapies.
Software engineering and automation engineering services including CSV support, automation testing, supervision system migration and technical support for instrumentation and metrology.
Medical writing for clinical development documents and technical writing for device documentation, installation and service procedures.
Expertise Areas
- Quality assurance and GMP readiness
- Project and program management (PMO)
- Process engineering and bioprocessing
- IT systems and CSV automation
Key Technologies
- Computer System Validation (CSV)
- Automation and supervisory systems migration
- Quality Management Systems (QMS)
- Upstream and downstream bioprocessing