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Queen’s House Consulting has extensive experience in the pre-clinical development of new biological and biotechnology products.
We can help your product on its journey from laboratory bench through pilot manufacture to clinical trial and licence. At each development transition, Queen’s House Consulting can advise on the requirements for effective technology transfer between the sponsor and the supplier.
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How to optimise your laboratory discovery for viable clinical evaluation and commercial industrialisation;
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What is required at each stage and scale in the development;
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How to avoid problems later by planning solutions sooner;
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Bioprocess design, development and optimisation;
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Technical agreements between the programme sponsor and their suppliers;
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Engagement with regulatory authorities to satisfy their expectations.
Please contact Queen’s House Consulting to discuss your specific requirements.
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