Your trusted partner in Pharmaceutical Engineering
About Us
Streamlining Complex Pharma Validation Processes
We offer a comprehensive suite of integrated pharmaceutical engineering services that go significantly beyond basic oversight, providing proactive, end-to-end support throughout the entire validation and project lifecycle, from concept to operational readiness. Our mission is to empower your pharmaceutical innovations by ensuring unwavering reliability, full regulatory compliance, and sustained operational excellence.
Our Services
Factory Acceptance Test (FAT) Support
Our experienced team provides comprehensive support throughout the entire Factory Acceptance Test (FAT) lifecycle. We offer meticulous assistance with pre-FAT preparations, diligent on-site execution, and thorough post-FAT activities to ensure your equipment meets all specifications prior to shipment.
Learn More
Comprehensive Validation Services
Intelion’s multidisciplinary team delivers expert validation services across the full project lifecycle. From URS creation and Design Qualification (DQ) through to FAT, Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), we ensure rigorous compliance and efficient project delivery. Our capabilities are founded on deep expertise in CQV, electrical engineering, automation, and quality assurance.
Learn More
Pharmaceutical Project Management
Our dedicated Project Managers, with specialized experience in pharmaceutical engineering, are committed to delivering your projects on schedule and within budget. They employ proven methodologies and remain current with leading industry tools and practices to optimize efficiency, manage resources effectively, and ensure transparent communication.
Learn More
AI/ML Validation Platform (Coming Soon)
Intelion is at the forefront of innovation, developing a proprietary AI/ML-powered SaaS platform designed to revolutionize pharmaceutical validation. While full details are forthcoming, this cutting-edge solution will leverage computer vision and machine learning to significantly enhance automation, data integrity, and traceability within validation processes, all while adhering to the highest industry standards.
Learn More
Why choose Intelion?

Integrated Multidisciplinary Expertise

Our team comprises seasoned engineers and specialists across CQV (Commissioning, Qualification, and Validation), Electrical Engineering, Automation, and Quality Assurance. This integrated expertise ensures a holistic and technically sound approach to your pharmaceutical engineering and validation challenges, delivering robust and compliant solutions.


Proven Success in Complex Pharmaceutical Projects: 


Intelion has a demonstrated history of successfully navigating and delivering a wide range of demanding pharmaceutical engineering and validation projects. We partner with clients to overcome complex regulatory landscapes and technical hurdles, consistently achieving project goals efficiently and effectively.


Client-Centric, Tailored Solutions

We recognize that every pharmaceutical project has unique requirements and objectives. Intelion is committed to deeply understanding your specific needs, customizing our comprehensive suite of services to deliver optimal outcomes, clear communication, and maximum value for your investment.


Unwavering Commitment to Quality and Compliance

Our dedication to excellence is fundamental to everything we do. We are committed to delivering the highest quality in every aspect of our service, ensuring full adherence to stringent regulatory requirements (GxP, FDA, EMA) and striving to exceed your expectations for project success and operational readiness.


End-to-End Lifecycle Support & Strategic Problem Solving

Intelion provides comprehensive support throughout the entire project lifecycle – from initial concept, user requirements, and design, through to commissioning, qualification, and ongoing operational support. We excel at identifying critical bottle necks and implementing effective solutions to ensure smoother, more efficient validation processes and project execution.