Your Partner all along the Development Cycle of your Innovative Pharmaceutical Product
From early stage proof of concept to pre-clinical or clinical development
Bio Elpida,
expert CDMO in innovative cell therapy and cell culture and approaches, can be, according to your needs,
your partner all along the development cycle of your innovative pharmaceutical product with services that include:
The expertise of Bio Elpida enables us to accompany you all along the process
Thanks to the expertise of its team, Bio Elpida can be your partner from early stages to clinical transfer:
New concept
Technical Evaluation
Regulatory Study
Elaboration of Development plan
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Pharmaceutical R&D
Process
Quality Control
Optimisation
Support Documentation
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Pharmaceutical Feasibility
Process Consolidation
QC Tests Consolidation
Processes Writting
GMP Pre-validation
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GMP to Clinical Transfer
Process Validation
Analytical Validation
IMPD Writting
Clinical Batches Manufacturing
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Working with Bio Elpida means more than services
Reaching your goals, timelines and budget is the minimum to expect from a service company. At Bio Elpida, the project managers and the expert teams ensure that you benefit from our extensive knowledge and experience. We operate as an extension of your company and take your problems as ours.
Hence, from a simple piece of contract service to the most complex issue in cell culture, Bio Elpida endeavours to provide you with the highest quality work possible within the following range of cell culture and cell therapy services.