Replies to post #61386 on Therapeutic Solutions International Inc (TSOI)

[centsability4me]

getting into the trends on bio.

every Bio startup has a past.

a lot of posters can't put the log on the table and mill it.

each product has it's own DD Chain / timeline.

most diggers know the timeline on each of the TSOI products.


the comments from those that want more daily action are welcome.
and why it doesn't move @ 20M share trades in total trades per trading day.

[BigBadWolf]

Ukeep asking 4then runaway from CommonCents as2 why?

https://investorshub.advfn.com/boards/read_person.aspx?membernum=157766

50 Shades of Avoidance pick 1 & try not to be scared

[BigBadWolf]

CommonCents 2wonder what his like(s) mightB
https://investorshub.advfn.com/boards/read_msg.aspx?message_id=172434313&txt2find=Weiss

munchies

sidekick(s)

Right Doc


SPRs initialed on the Do:-Dg tags

[BigBadWolf]

Clinical trials registers such as ClinicalTrials.gov and portals to trials registers such as the World Health Organization (WHO) International Clinical Trials Registry Platform (ICTRP) are increasingly used to identify ongoing or completed clinical trials.

https://www.who.int/clinical-trials-registry-platform

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4076126/#:~:text=Clinical%20trials%20registers%20such%20as,ongoing%20or%20completed%20clinical%20trials.

ClinicalTrials.gov is a website and online database of clinical research studies and information about their results. The National Library of Medicine (NLM) maintains the website

https://clinicaltrials.gov/

https://investorshub.advfn.com/boards/read_msg.aspx?message_id=172658064&txt2find=Clinical%20trial

https://www.businesswire.com/news/home/20230515005454/en/

Clinical Stage Biotech Company Partners with Premier Compounding Pharmacy to Provide Doses for IRB Cleared Phase I/II Clinical Trial

Institutional Review Board
Under FDA regulations, an Institutional Review Board is group that has been formally designated to review and monitor biomedical research involving human subjects. In accordance with FDA regulations, an IRB has the authority to approve, require modifications in (to secure approval), or disapprove research.Sep 11, 2019

Institutional Review Boards (IRBs) and Protection of Human ...

Food and Drug Administration (.gov)
https://www.fda.gov › about-fda › institutional-review-b...

There are three types of IRB review: Expedited, Exempt and Full Board. Expedited review is only allowed for research projects that are no more than minimal risk and will be reviewed by an IRB Chair or Chair Designee (IRB Member).

What does IRB mean in medical research?
The Institutional Review Board (IRB) is an administrative body established to protect the rights and welfare of human research subjects recruited to participate in research activities conducted under the auspices of the institution with which it is affiliated.