Your Partner all along the Development Cycle of your Innovative Pharmaceutical Product

Bio Elpida, your CMO expert for R&D and pre-clinical and clinical development

Bio Elpida, expert CMO in innovative cell therapy, cell culture and immunology approaches, can be, according to your needs, your partner all along the development cycle of your innovative pharmaceutical product:

• R&D and feasibility
 

• Pharmaceutical development
 

• Manufacturing and control of clinical and small scale marketing batches
 

• Immuno-testing and analytical tests
 

• Additional support such as bulk purification, fill and finish, formulation, analytical development and regulatory services

New concept • Technical Evaluation • Regulatory Study • Elaboration of Development plan

Pharmaceutical R&D • Process • Quality Control • Optimisation • Support Documentation

Pharmaceutical Feasibility • Process Consolidation • QC Tests Consolidation • Processes Writting • GMP Pre-validation

GMP to Clinical Transfer • Process Validation • Analytical Validation • IMPD Writting • Clinical Batches Manufacturing

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.