Zera Verification

Kuti ushandise webhusaiti yeANDUVAPE unofanirwa kunge uine makore makumi maviri nerimwe kana kupfuura.Ndokumbira utarise zera rako usati wapinda pawebhusaiti.

Zvigadzirwa zviri pawebhusaiti ino zvakagadzirirwa vanhu vakuru chete.

Tine urombo, zera rako haribvumidzwe

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FDA Muchidimbu: FDA Inoyambira Mafemu Nekuramba Achishambadzira E-fodya Zvigadzirwa Mushure mekunge Agency Yaramba Mvumo.

“FDA ndiyo ine basa rekuona kuti fodya itsva yaiswa muhurongwa hwakakodzera hwekuongorora kana ichizadzisa zvinodiwa nemutemo wezveutano isati yatengeswa.Kana chigadzirwa chikasasangana neiyo mwero saka agency inopa rairo yekuramba kushambadzira application.Hazvisi pamutemo kutengesa fodya itsva muUnited States iyo isina mvumo yekushambadzira kubva kuFDA.

Chimwe chatinonyanyokoshesa kuona kuti vanogadzira fodya vane mhosva yekutengesa fodya isingatenderwe.Chiitiko chanhasi chinoratidza kuti tiri kukoshesa kuomeserwa kune vagadziri vefodya vakagamuchira chiito chisina kunaka pachikumbiro chavo, senge Marketing Denial Order kana Refuse to File notification uye kuramba tichitengesa zvisiri pamutemo zvigadzirwa izvo zvisina mvumo, pamwe nezvigadzirwa zvakakundikana vagadziri. kuendesa chikumbiro chekushambadzira.

Ibasa redu kuona kuti vagadziri vefodya vatevedzera mutemo wekuchengetedza hutano hweveruzhinji uye ticharamba tichipa makambani mhosva yekutyora mutemo.”

Mamwe Mashoko

● Nhasi, US Food and Drug Administration yakapa tsamba dzenyevero kumakambani makumi maviri kuti arambe achitengesa zvisiri pamutemo zvemagetsi nicotine delivery system (ENDS) zvigadzirwa zviri nyaya yeMarketing Denial Orders (MDOs).Aya ndiwo mabhii ekutanga yambiro akapihwa kune zvigadzirwa zviri pasi peMDO zvakatemerwa pane yavo premarket fodya chigadzirwa application (PMTAs).

● FDA yapawo tsamba dzechenjedzo nhasi nezvekutengeswa kwefodya zvisiri pamutemo kune imwe kambani yakawana zvisungo zve Refuse to File (RTF) paPMTA yavo, kambani imwe yakagamuchira RTF neMDO zvisungo paPMTA yavo, uye makambani matanhatu asina kutumira. chero premarket application.

● Pamwe chete, aya makambani makumi maviri nemasere akaronga hwerengedzo yakabatanidzwa yezvigadzirwa zvinopfuura 600 000 neFDA.

● Kubva munaSept. 23, FDA yakabudisa huwandu hwe323 MDOs, inotora zvinopfuura 1,167,000 flavoured ENDS zvigadzirwa.

● Iyo FDA icharamba ichikoshesa kumanikidza kumakambani anotengesa zvigadzirwa zveENDS pasina mvumo inodiwa-kunyanya izvo zvigadzirwa zvine mukana wekushandiswa kwevechidiki kana kutanga.


Nguva yekutumira: Jan-10-2022