Team Consulting

Team Consulting is a medical device development consultancy with over 40 years of experience creating healthcare products across drug delivery, MedTech, surgical devices, diagnostics, digital health, and cell and gene therapies. The company employs more than 130 in-house specialists including human factors engineers, mechanical engineers, regulatory experts, and industrial designers.

The firm provides end-to-end product development services from front-end innovation and strategy through industrialization and launch. Team Consulting holds ISO 13485 certification and works with clients ranging from major pharmaceutical companies like AstraZeneca and Chiesi to emerging healthcare startups. Their approach emphasizes user-centered design combined with engineering excellence and regulatory compliance.

The company has contributed to multiple award-winning medical devices and maintains active involvement in industry standards through participation on international committees. They have achieved Bronze EcoVadis certification for sustainability practices and offer sustainable engineering services to help clients meet environmental goals.

Choose Team Consulting when your medical device development requires deep regulatory expertise combined with user-centered design. Their 40-year track record and ISO 13485 certification make them particularly suited for clients navigating complex regulatory pathways while maintaining focus on end-user adoption.

Expect a collaborative engagement model where Team acts as an extension of your internal team, bringing multidisciplinary expertise to solve technical challenges. Their involvement in industry standards bodies and work with both major pharma and startups indicates flexibility in accommodating different organizational needs and project scales.

Team Consulting operates exclusively in healthcare, focusing on medical device and combination product development. Their expertise spans critical healthcare verticals including drug delivery systems, surgical devices, diagnostics, digital health technologies, and emerging cell and gene therapy devices. The company's ISO 13485 certification and 40-year healthcare focus demonstrate deep understanding of medical device regulatory requirements, quality management systems, and clinical workflows across the continuum of care from prevention through treatment.

The ideal client is a pharmaceutical company, medical device manufacturer, or well-funded healthcare startup developing complex medical devices or combination products that require regulatory compliance expertise. Organizations seeking partners who can handle both the technical engineering challenges and human factors considerations while maintaining quality management systems will find strong alignment with Team's capabilities.