@warrenbluffet Yes, correct. FDA does not have to approve marketing material. As is here in AU, the TGA will hold you responsible if your marketing does not meet its criteria. However, requiring approval on marketing/advertising material would simply not be feasible. I am the sponsor of a medtech device from Europe and have been through the AU process.
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The re-rate journey, page-51
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Last
2.7¢ |
Change
0.000(0.00%) |
Mkt cap ! $20.21M |
Open | High | Low | Value | Volume |
2.7¢ | 2.7¢ | 2.6¢ | $24.66K | 945.4K |
Buyers (Bids)
No. | Vol. | Price($) |
---|---|---|
3 | 315442 | 2.6¢ |
Sellers (Offers)
Price($) | Vol. | No. |
---|---|---|
2.7¢ | 1463859 | 3 |
View Market Depth
No. | Vol. | Price($) |
---|---|---|
1 | 1885 | 0.027 |
3 | 315442 | 0.026 |
9 | 1016132 | 0.025 |
1 | 1238229 | 0.024 |
2 | 40943 | 0.023 |
Price($) | Vol. | No. |
---|---|---|
0.026 | 1886 | 1 |
0.027 | 1426859 | 2 |
0.028 | 190000 | 1 |
0.029 | 77542 | 2 |
0.030 | 221800 | 1 |
Last trade - 15.59pm 24/06/2025 (20 minute delay) ? |
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