RE: RE RE: Update due soon25 Apr 2021 16:47
The company has been working with PYC for about 15 years. Very capable bunch. However, the data always needs to go through committee including the company, as a sponsor, with a leading, nominated person, well qualified medical third party monitor person, resgulator, hospital etichs committee, principal investigator etc. When you have done all that then you have a chance of being on the top of the data, which is generated during several years. On the whole, the committee has a conf call about once a week a so, and they tend to question (person) involved in clinical trials very hard.