About Us & Our Team
Want an experienced team to help with product development, manufacture, launch and supply?
HiTech Health has the knowledge and expertise to help with product development and ensure all CMC related operational activities are completed on time. We can save you time and money when compared to building this expertise internally.
Our cell and gene therapy expertise extends beyond services to include process and analytical development at our state-of-the-art laboratory.
Industry Expertise
Looking for an experienced team that can help with all aspects of CMC product development?
HiTech health has the in-house experts that can help from pre-clinical through a successful product registration and launch. We can help with 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, QP approval and management of supply chain through to your distributor.
We can provide experts who know what needs to be done and can help you to meet project goals and timelines. This approach can save you time and money.
Team
Brian Harrison
DirectorAoife Duffy
Cell and Gene Therapy Operations ManagerCatherine Hanley
EHS ConsultantColin Henehan
Operations ConsultantDamian Greene
Operations & Strategy ConsultantJulie-Anne O'Neill
Quality and Compliance LeadLeonora Bishop
Business Development ManagerMichelle Allen
External Manufacturing ConsultantAmina Al-Mossawi
Qualified Person (QP)Hitech Health Appoint Clare O’Sullivan as Global Head of Commercial
Hitech Health is delighted to announce the appointment of Clare O’Sullivan as Global Head of Commercial. Brian Harrison, Managing Director of HiTech Health, commented on Clare’s appointment: “I am pleased to announce the appointment of Clare O’Sullivan as Global Head...
New FDA ‘Super Office’ created for Cell and Gene Therapy Products
The continued growth in the development of cell and gene therapies (CGTs) has led to an exponential increase in the workload of the organisations involved. As ClinicalTrials.gov. indicates, there will be more than 1,000 ongoing clinical trials for CGTs registered in...
Importation of Medicinal Products: Understanding the EU requirements
The manufacturing of medicinal products for the EU market frequently occurs outside the EU zone and this presents logistics and regulatory considerations for the product owner. All stages of manufacturing medicinal products in third countries should be carried out in...
Telephone
IE: +353-1-9631489
UK: +44-20-30267419
US: +1-857-3265835
Contact us
Get in touch anytime – we are always available to discuss your upcoming projects.