Periodic Reporting for period 1 - Refeed (Customised lipid supplementation of culture media for efficient in vitro cell culture applications)
Berichtszeitraum: 2017-01-01 bis 2017-04-30
Refeed is a customizable ethanol-based lipid supplement for in-vitro cultures, capable of addressing major culturing issues and/or boost specific bioprocesses. Tailored Refeed formulations can be adapted to any cell culture conditions and can be animal-free, fully synthetic and, upon completing the Phase 2 project, GMP-grade.
Remembrane reviewed the overall objectives outlined to scale-up its business, and adjusted them on the basis of the interaction with prospect stakeholders. The goal of the product development plan is to generalise and validate the process for the deployment of customized Refeed supplements in order to serve small, medium and large players on a global dimension in extremely reduced time (3 working days for production and worldwide shipment).
Between 1st January 2017 and 30th April 2017, Remembrane undertook a full feasibility study of its Refeed business project, planned the strategy for its scale up and commercialization, and contacted many stakeholders in the biotechnology industry to assess the technical and economic viability of its product.
The first result was the identification of the Cell Therapy industry as the most appealing market sector for Refeed, given the market condition and the possibility of fine-tuning the Refeed supplement for each therapy under development: in the Cell Therapy industry Refeed can be highly competitive, the market itself is boosting, and the players in the field are easier to be reached, since they are often medium-size enterprises, instead of big pharma companies as it is in the vaccine market, for instance. Another important result was the recognition that, as a supplier of cell therapy companies, each with their own specific needs, Remembrane will need flexible scale-up capabilities for the Refeed production, and a GMP (Good Manufacturing Practice) compliant production process. This led to the redefinition of a few objectives of the feasibility assessment. During Phase 1 project a great effort was made by Remembrane to identify preliminary features and potential stakeholders to fully engineer the automated production line for Refeed, and the steps required for the GMP compliance were mapped.