The document has to contain details of:
All the pre-clinical experiments, their purposes and their results, all the clinical trials, the trial process, each patient how dosed and how tested and results. Process for assessing the results of the trials
Manufacturing process, process audits for all parties involved in manufacture, etc etc.
AGM, page-30
-
- There are more pages in this discussion • 5 more messages in this thread...
You’re viewing a single post only. To view the entire thread just sign in or Join Now (FREE)
Add SPL (ASX) to my watchlist
 (20min delay)
|
|||||
|
Last
9.5¢ |
Change
0.000(0.00%) |
Mkt cap ! $39.17M | |||
| Open | High | Low | Value | Volume |
| 0.0¢ | 0.0¢ | 0.0¢ | $0 | 0 |
Buyers (Bids)
| No. | Vol. | Price($) |
|---|---|---|
| 1 | 5684 | 10.0¢ |
Sellers (Offers)
| Price($) | Vol. | No. |
|---|---|---|
| 9.7¢ | 56840 | 1 |
View Market Depth
| Last trade - 09.50am 24/07/2024 (20 minute delay) ? |
| SPL (ASX) Chart |
Day chart unavailable