Section 9
Recommendation Letter To Be Obtained For Exportation Or Importation of Drug
Any person who intends to export or import a drug shall, prior to obtaining the export or import license pursuant to the prevailing law, obtain a recommendation letter from the Department, as prescribed, on payment of the prescribed fees.
Drugs Act, 2035, (1978
Chapter - 4
Section 7: Recommendation Letter To Be Obtained To Establish Drug IndustrySection 8: Product License To Be ObtainedSection 8A: registration Of DrugSection 9: Recommendation Letter To Be Obtained For Exportation Or Importationof DrugSection 10: Registration Of Name For Sale And Distribution Of DrugSection 10A: Sale And Distribution Of Registered Drugs OnlySection 11: validity Period And Renewal Of Product License, Recommendation Letterand Certificate
Chapter - 5
Section 12: Drugs To Be Safe For Public Consumption, Efficacious And Of Quality StandardSection 13: Prohibition On Manufacture, Sale, Distribution, Export, Import, Storage Or Consumption Of Drug Not Conforming To Prescribed StandardSection 14: Return Of Drug Which Is Not Safe For Public Consumption, Efficacious And Of Quality StandardSection 15: Provision Of CompensationSection 16: submission Of Letter Of Guarantee To DepartmentSection 17: Categorization Of DrugsSection 18: Prohibition On Misuse Or Abuse Of DrugsSection 19: Prohibition On False Or Misleading Advertisement Of Drugs
Chapter - 7
Section 25: powers Of Government Of Nepal To Prohibit Manufacture, Sale,distribution, Storage, Transportation, Export, Import Or Consumption OfdrugsSection 26: Powers To Fix Price Of DrugSection 27: Provisions Relating To PrescriptionSection 28: Prohibition On Manufacture, Sale, Distribution, Dispensing Or Storagewithout Making Arrangement Of Required Human Resource♦ ♦ Orresource SSection 29: Prohibition On Adulteration In Drugs And Sale Of Adulterated DrugsSection 30: Prohibition On Sale Or Distribution Of Date Expired DrugsSection 31: License To Be Obtained From Department For Clinical Trial Of New DrugSection 32: Disclosure Of System Of Drug And Other Particulars While Manufacturing DrugSection 33: Narcotic And Poisonous Drug To Be Kept SafelySection 34: PenaltiesSection 35: Ceiling Of Fine And Imprisonment In Lieu Of FineSection 36: Right To Register Patent Of DrugSection 37: Delegation Of AuthoritySection 38: Government To Be The PlaintiffSection 39: Investigation And Filing Of CaseSection 40: Power To Frame Rules