| 1. | 通報(bào)成員：菲律賓 |
| 2. | 負(fù)責(zé)機(jī)構(gòu)：ENGR. ANA TRINIDAD F. RIVERA；Director IV；Center for Cosmetics Regulation and Research (CCRR)；Food and Drug Administration；DEPARTMENT OF HEALTH |
| 3. |
通報(bào)依據(jù)的條款：Article 2.9.2 [X], 2.10.1 [??], 5.6.2 [??], 5.7.1 [??]
通報(bào)依據(jù)的條款其他：
|
| 4. | 覆蓋的產(chǎn)品：Vapor products; Tobacco, tobacco products and related equipment (ICS 65.160)
ICS：[] HS：[] |
| 5. |
通報(bào)標(biāo)題：Guidelines for the Issuance of Pre-application Documentary Evaluation (PADE) for Vapor Products Seeking Registration under FERN 1 with the Center for Cosmetics Regulation and Research頁數(shù)：5 使用語言：英語 鏈接網(wǎng)址： |
| 6. |
內(nèi)容簡述： This Circular is being issued to provide supplemental procedures and guidelines for the issuance of a Pre-application Documentary Evaluation (PADE) certificate as part of the requirements for vapor product refills and cartridges under FDA Electronic Registration Number Category (FERN1) authorization and shall apply to all manufacturers, traders and importers seeking to apply for a FERN 1 authorization of their vapor product refills and cartridges. |
| 7. | 目的和理由：Protection of human health or safety; Reducing trade barriers and facilitating trade; Other |
| 8. | 相關(guān)文件： Republic Act No. 9711 - FDA Act of 2009 Section II of Executive Order No. 106? |
| 9. |
擬批準(zhǔn)日期：
This Circular shall take effect 15 days after publication in a newspaper of general circulation and the Office of National Administrative Register of the UP Law Center. 擬生效日期： This Circular shall take effect 15 days after publication in a newspaper of general circulation and the Office of National Administrative Register of the UP Law Center. |
| 10. | 意見反饋截至日期：60 days from notification |
| 11. |
文本可從以下機(jī)構(gòu)得到：
MR. NEIL P. CATAJAY https://members.wto.org/crnattachments/2020/TBT/PHL/20_5073_00_e.pdf |
This Circular is being issued to provide supplemental procedures and guidelines for the issuance of a Pre-application Documentary Evaluation (PADE) certificate as part of the requirements for vapor product refills and cartridges under FDA Electronic Registration Number Category (FERN1) authorization and shall apply to all manufacturers, traders and importers seeking to apply for a FERN 1 authorization of their vapor product refills and cartridges.
粵公網(wǎng)安備 44010602010620號