We are a GMP-certified Contract Development and Manufacturing Organisation (CDMO) specialising in advanced therapies, including cell and gene therapies.

Our team provide professional consulting services to support with product development, launch and supply across the advanced therapy, pharmaceutical, biotechnology, and medical device sectors.

Our highly experienced, cross-functional team provides end-to-end support from preclinical development through to commercial product launch. We bring deep expertise across a broad range of advanced therapies, including both autologous and allogeneic cell therapies. In addition, our in-house team of Qualified Persons (QPs) are available to perform batch certification and ensure regulatory compliance for global supply.

Industry Expertise

Looking for an experienced team that can help with all aspects of product development?

HiTech health has the in-house experts that can help from pre-clinical through a successful product registration and launch. We provide both CDMO solutions as well as consulting services for product development strategy creation right through to day-to-day project management.

Our team have led the development, manufacture and supply of multiple products including cell and gene therapies for clinical trials and also the supply of approved medicines to patients.

Partner of Choice

HiTech Health can provide a team to enable all the activities including product importation, EU and UK QP approval and management of supply chain through to patients. We have a proven track record of delivering exceptional results for global clients as they develop, scale-up, manufacture and supply their therapies internationally. 

We can provide Subject Matter Experts (SMEs) who know what needs to be done and can help you to meet project goals and timelines. Our team have deep knowledge and understanding of Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) requirements.