Clinical Packaging, Labelling and Distribution

HiTech Health offers clinical packaging, labelling and distribution solutons for your medicinal product. Our EU GMP-certified facility can support your clinical packaging needs and integrates seamlessly with our QP batch release services. 

Clinical Packaging and Labelling under GMP conditions

HiTech Health supports companies undertaking a wide range of clinical studies, from small open-label Phase 1 through to larger Phase 3 studies. Our experienced team based at our EU GMP-certified facility are committed to ensuring that your clinical materials are packaged to the highest standards of quality and compliance. If you’d like to find out more about how we can support your clinical packaging requirements then get in touch with us today.

QP release and Distribution to Sites

 

Following clinical packaging and labelling activities, our team of QPs can perform batch certification to enable your therapy to be used in clinical trials in the EU, UK and Rest of World (RoW) markets. HiTech Health are uniquely positioned to offer end-to-end integrated solutions to allow for the seamless delivery of therapies to patients. Our in-house supply chain team can support you with managing distribution and logistics activities in accordance with Good Distribution Practice (GDP).

Cell and Gene Therapy Manufacturing

HiTech Health are delighted to have an article entitled 'Cell and Gene Therapy Manufacturing Considerations for Early Stage Companies' published in distinguished publications, cellandgene.com and outsourcedpharma.com. The article should be of benefit to companies who...

2024 ATMP Review

Over the past decade, the regenerative medicine landscape has undergone an extraordinary evolution with the continuous growth of Advanced Therapeutic Medicinal Products (ATMPs). ATMPs are medicines for human use that are based on genes, tissues or cells. They treat...

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