You are viewing the translated version of औषधिको पेटेण्ट दर्ता गर्ने अधिकार.
Section 36
The right to register a drug patent
The right to register a drug patent will be in accordance with the prevailing law.
Drugs Act, 2035, (1978
Preamble - 0
Chapter - 4
Section 7: Need to get a letter of recommendation to establish a pharmaceutical industrySection 8: required to obtain production licenseSection 8A: Medicines to be registeredSection 9: A prescription should be obtained to import the drugSection 9A: Emergency Use of Medicines and VaccinesSection 10: Name to be registered to sell-distribute medicineSection 10A: Only registered medicines should be sold and distributedSection 11: Duration and Renewal of Product Licenses, Recommendations and Certificates
Chapter - 5
Section 12: Medicines should be public safe, effective and efficientSection 13: Prohibition of production, sale-distribution, export-importation, or consumption of drugs that do not have the prescribed levelSection 14: Returning medicines that are not safe, effective or efficient for the publicSection 15: Compensation to be paidSection 16: Document of assurance to be submitted to the departmentSection 17: Medicines can be divided into groupsSection 18: No improper use or abuse of medicineSection 19: No false or misleading advertising of medicines
Chapter - 6
Section 20: which the inspector may examine and inspectSection 20A: can be investigated and inspected by inspectors appointed by the state governmentSection 21: who can appeal on the order of the administratorSection 22: Procedures to be adopted during inspection or investigationSection 23: Qualifications for inspectors and analystsSection 24: Sending drug samples for testing
Chapter - 7
Section 25: The Government of Nepal may prohibit the production, sale, distribution, storage, transportation, export, import or consumption of drugsSection 26: TheSection 27: Arrangements related to giving prescriptionsSection 28: Production, sale-distribution, dispensing or storage of medicine should not be done without gathering the necessary manpower and equipmentSection 29: Adulteration of drugs and adulterated drugs not to be soldSection 30: Expired medicines should not be soldSection 31: License required for clinical trials:Section 32: Drug system and other things to be disclosedSection 33: to preserve applicable and poisonous drugsSection 34: Penalty PunishmentSection 35: Upper limit of fine and imprisonment for fineSection 36: The right to register a drug patentSection 37: Delegation of authoritySection 38: GovernmentalistSection 39: Case study and scopeSection 40: Power to make rules