CGT Training
One of the biggest bottlenecks in the CGT space is finding the right people. HiTech Health offers a unique range of personalised hands-on training in CGT at our GMP-ready Process Development laboratory.
CGT Training under GMP conditions
We can train your personnel on all aspects of CGT, from tissue procurement and isolation techniques, cell culturing and scale up, cell counting, cryopreservation techniques, as well as other quality control assays and cleanroom behaviour. We have access to many different types of starting tissues for CGT and have these procured for your specific needs and training. As well as having experts in the CGT space, we also have a team of trainers focused on the GMP aspects and this can help your team get trained on your manufacturing process within a cleanroom environment.
On-Site Training
Training can be personalised to your manufacturing needs and if preferred, our experts can travel to your manufacturing site and perform training there. We can offer hands-on cleanroom behaviour training as well as aseptic practices and can do a gap analysis for the client to see where improvement or modifications are needed. A core training module also delivered by our experts is GMP training and the GMP requirements needed by operators. Whatever your training needs are, HiTech Health are here to help and train your staff.
Good Distribution Practice (GDP): 3 Considerations for Ensuring Compliance
Ensuring product quality and integrity is maintained throughout the end-to-end supply chain of medicinal products is imperative. The system for managing quality should encompass the organisational structure, procedures, processes and resources, as well as activities...
HiTech Health presented at the 3rd Global Bioprocessing, Bioanalytical, and ATMP Manufacturing Congress in Dublin, Ireland
HiTech Health are delighted to have attended the 3rd Global Bioprocessing, Bioanalytics and ATMP Manufacturing Congress on 16th and 17th May. HiTech Health’s Quality and Compliance Lead Julie-Anne O'Neill and Manager of Cell and Gene Therapy Operations Aoife Duffy...
Understanding the New EU Clinical Trial Regulation (CTR)
On the 31st January 2022, The Clinical Trials Regulation ((Regulation (EU) No 536/2014)) became effective and replaced the previous Directive (EC) 2001/20/EC and corresponding national legislation. The Clinical Trials Regulation (CTR) coordinates the review and...
Telephone
IE: +353-1-9631489
UK: +44-20-30267419
US: +1-857-3265835
Stay Up To Date
Connect with us to receive the latest HiTech Health and industry updates.