दफा ५
Department Of Drug Administration
(1) Government of Nepal shall establish a Department of Drug Administration for the implementation of the objectives of this Act.
(2) The Department established pursuant to Sub-section (1) shall carry out all the functions related with the control of drugs under this Act and the Rules framed there under.
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♣ Amended by the First Amendment.
(2) The Department established pursuant to Sub-section (1) shall carry out all the functions related with the control of drugs under this Act and the Rules framed there under.
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♣ Amended by the First Amendment.
Drugs Act, 2035, (1978
परिच्छेद - ४
दफा ७: Recommendation Letter To Be Obtained To Establish Drug Industryदफा ८: Product License To Be Obtainedदफा ८क: registration Of Drugदफा ९: Recommendation Letter To Be Obtained For Exportation Or Importationof Drugदफा १०: Registration Of Name For Sale And Distribution Of Drugदफा १०क: Sale And Distribution Of Registered Drugs Onlyदफा ११: validity Period And Renewal Of Product License, Recommendation Letterand Certificate
परिच्छेद - ५
दफा १२: Drugs To Be Safe For Public Consumption, Efficacious And Of Quality Standardदफा १३: Prohibition On Manufacture, Sale, Distribution, Export, Import, Storage Or Consumption Of Drug Not Conforming To Prescribed Standardदफा १४: Return Of Drug Which Is Not Safe For Public Consumption, Efficacious And Of Quality Standardदफा १५: Provision Of Compensationदफा १६: submission Of Letter Of Guarantee To Departmentदफा १७: Categorization Of Drugsदफा १८: Prohibition On Misuse Or Abuse Of Drugsदफा १९: Prohibition On False Or Misleading Advertisement Of Drugs
परिच्छेद - ७
दफा २५: powers Of Government Of Nepal To Prohibit Manufacture, Sale,distribution, Storage, Transportation, Export, Import Or Consumption Ofdrugsदफा २६: Powers To Fix Price Of Drugदफा २७: Provisions Relating To Prescriptionदफा २८: Prohibition On Manufacture, Sale, Distribution, Dispensing Or Storagewithout Making Arrangement Of Required Human Resource♦ ♦ Orresource Sदफा २९: Prohibition On Adulteration In Drugs And Sale Of Adulterated Drugsदफा ३०: Prohibition On Sale Or Distribution Of Date Expired Drugsदफा ३१: License To Be Obtained From Department For Clinical Trial Of New Drugदफा ३२: Disclosure Of System Of Drug And Other Particulars While Manufacturing Drugदफा ३३: Narcotic And Poisonous Drug To Be Kept Safelyदफा ३४: Penaltiesदफा ३५: Ceiling Of Fine And Imprisonment In Lieu Of Fineदफा ३६: Right To Register Patent Of Drugदफा ३७: Delegation Of Authorityदफा ३८: Government To Be The Plaintiffदफा ३९: Investigation And Filing Of Caseदफा ४०: Power To Frame Rules