We are maintaining a database of people who have expressed interest in NTCELL for Parkinson’s disease so that we may provide them with relevant information if we are successful in obtaining provisional consent to treat paying patients.
Great news , So a pseudo Patient Register? Potential Customers who have expressed interest. The Business Unit will have Database to start with, so avoids a standing start for commercialisation. Would be nice to Know how many people have expressed/registered their interest but happy to hear a database has begun.
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