Cell and Gene Therapy
We are a Contract Development and Manufacturing Organisation (CDMO) for advanced medicines including cell and gene therapies. With our in-depth knowledge and experience of Cell and Gene Therapy products, HiTech Health offer a range of services to help develop and supply life-changing treatments.
Process and Analytical Assay Development
Our experts can provide comprehensive solutions and strategies for process development, supply pre-clinical products and quality control assay development.
Qualified Persons Specialising in CGT
Ensuring you have the right person to release your product to the clinic is essential for success and HiTech Health can support you with this critical role.
Audits of CDMOs and Contract Testing Laboratories
Let us help you to perform an independent audit of your key manufacturer or testing laboratory to ensure you are receiving a quality service.
CGT Training
One of the biggest bottlenecks in the CGT space is finding the right people. HiTech Health offer a unique range of personalised training in the CGT space.
Supply Chain Assessment for CGT
Cell and gene therapies are distinctly different from traditional biopharma product and their supply chains require uniquely designed logistics solutions.
GMP Manufacturing
We can provide a full GMP manufacturing service for ATMPs and offer quality and compliance services including QP release of products.
Clients & Collaborators
Temperature Controlled Transportation of Medicinal Products
Temperature is a critical parameter in the transportation and storage of medicinal products. The temperature must be controlled and monitored from the manufacturing site through to the distributor and site of medicine use. When temperatures go outside the specified...
Five Key Considerations When Selecting a Cell and Gene Therapy CDMO
Many Cell and Gene Therapy (CGT) companies outsource product development and manufacturing activities to a Contract Development and Manufacturing Organisation (CDMO). It is critical to ensure that an informed decision is made when selecting a CDMO to prevent future...
HiTech Health Authorised by the MHRA to Perform Batch Importation and Certification of Investigational Medicinal Products (IMPs)
HiTech Health today announced that the company has been granted a Manufacturer’s/Importation Authorisation (MIA) for Investigational Medicinal Products (IMP) by the Medicines and Healthcare Products Regulatory Agency (MHRA). The company is now authorised to perform...
Telephone
IE: +353-1-9631489
UK: +44-20-30267419
US: +1-857-3265835
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