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Cannabis Use Disorder Among First-Year Undergraduate Students in Gaborone, Botswana
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Declaration of Habit-Forming Drugs Order. Drugs and Related Substances Regulations. Export of habit-forming drugs. Form of permit. Any duly registered medical practitioner, dentist or chemist and druggist, and any duly qualified veterinary surgeon who is desirous of exporting from Botswana any habit-forming drug as defined in the Act other than prepared opium as defined in the Act , shall-. The form of permit to import or acquire habit-forming drugs as provided for in section 5 1 of the Act shall be as contained in the Second Schedule hereto. Permission is hereby granted to This Permit will expire on the Dated this It is a condition of this permit that drugs imported or acquired hereunder shall not be used by the person to whom the permit is issued otherwise than for medicinal or scientific purposes or for the purpose of being sold or supplied to some other person in accordance with the provisions of the Habit-forming Drugs Act. Exempted drugs. Eyedrops for inclusion in first-aid outfits consisting of a solution of 1 in 3, Perchloride of Mercury in Castor Oil with 0,5 per centum of Cocaine. Declaration of habit-forming drugs. Ecgonine, its esters and derivatives which are convertible to ecgonine and cocaine. Morphine-Methobromide and other pentavalent nitrogen morphine derivatives including in particular the morphine-N-oxide derivatives, one of which is Codeine-N-Oxide. The isomers, unless specifically excepted, of the drugs in this Schedule whenever the existence of such isomers is possible within the specific chemical designation. The esters and ethers of the drugs in this Schedule whenever the existence of such esters or ethers is possible. The salts of the drugs listed in this Schedule, including the salts of esters, ethers and isomers as provided above whenever the existence of such salts is possible. Drugs Advisory Board. Registration of drugs. Exemption from registration. Approval for the manufacture, etc. Records to be kept by manufacturer of drugs. Import, export and distribution of drugs. Labelling of drugs. Recall of drugs. Prescription of drugs. Dispensing of Schedule 1A and 1B drugs. Dispensing of Schedule 1C drugs. Dispensing of Schedule 2 drugs. Dispensing of drugs by nurses. Dispensing, general. Emergency supply of drugs. Registers and records. Clinical trials. Classification of drugs. Prescribed habit-forming drugs. Provided that intervals between meetings of the Board shall never be greater than three months. Approval for manufacture etc. Whenever the Director finds that any portion of any batch of drugs does not conform to the standards of identity, strength, quality and purity, or any other requirement specified in the documentation for registration, he may instruct the licensee to discontinue the sale of the remainder of the batch and, so far as is practicable, to recall any portion of the batch already sold. Schedule 1C drugs may only be dispensed or sold by a pharmacist upon a written prescription of a medical practitioner or dentist presented for dispensing within thirty days from the date of issue thereof, and for the supply of a quantity of the drug not in excess of that indicated on the prescription, and in any case not exceeding thirty days supply, and any such prescription shall be retained in the pharmacy for a period of not less than three years from the date of the last sale or dispensing:. Provided that where the prescribing medical practitioner or dentist is personally known to the dispensing pharmacist and is confirmed as being a medical practitioner or dentist, and the pharmacist is satisfied that it is impossible or impracticable to obtain a written prescription within a time that is reasonable in all the circumstances, he may dispense a prescription made by telephone or fascimile, in quantities not exceeding those stated above, on condition that a written prescription will be provided within 48 hours. Notwithstanding regulations 11, 12 and 13, registered and enrolled nurses in referral, district, primary, mine, mission and private hospitals, clinics, health posts and mobile clinics, may, in the exercise of their duties, dispense Schedule 1A, 1B, 1C, 2 and 3 drugs to patients, upon written prescription by a medical practitioner or a dentist. Dispensing general. Any appeal lodged in accordance with the provisions of section 14 of the Act or regulation 18 6 shall be lodged within thirty days after the date when the decision appealed against is communicated to the applicant. For the purposes of the Act and these Regulations drugs shall be classified in accordance with the lists set out in the First Schedule. For the purposes of the definition of 'habit-forming drug', section 3 1 b and Part III of the Act the drugs listed in the Second Schedule are declared to be banned habit-forming drugs. The forms to be used for the purposes of the Act shall be in accordance with the forms set out in the Third Schedule. This section of the article is only available for our subscribers. Please click here to subscribe to a subscription plan to view this part of the article. Citation 2. Export of habit-forming drugs 3. Export of habit-forming drugs Any duly registered medical practitioner, dentist or chemist and druggist, and any duly qualified veterinary surgeon who is desirous of exporting from Botswana any habit-forming drug as defined in the Act other than prepared opium as defined in the Act , shall- a furnish to the Minister a certificate from the government or administration of the importing country to the effect that such government or administration is satisfied that the consignment of such habit-forming drug is required solely for medicinal or scientific purposes, and that it approves of its importation; b obtain from the Minister a permit under section 4 4 of the Act in the form in the First Schedule hereto. Form of permit The form of permit to import or acquire habit-forming drugs as provided for in section 5 1 of the Act shall be as contained in the Second Schedule hereto. Minister This Permit is not transferable. Exempted drugs Schedule HCN , Exempted drugs The preparations listed in the Schedule shall be exempted from the provisions of the Act. Emplastrum Opii B. Linimentum Opii B. Liniment of Opium. Linimentum Opii Ammoniatum B. Pasta Arsenicalis B. Arsenical Paste. Pilulae Hydrargyri cum Opio B. Pilulae Ipecacuanhae cum Scilla B. Pills of Ipecacuanha with Squills. Pilulae Plumbi cum Opio B. Lead and Opium Pills. Pilulae Digitalis et Opii Compositae B. Pilulae Hydrargyri cum Creta et Opii B. Pills of Mercury with Chalk and Opium. Pulvis Cretae Aromaticus cum Opio B. Aromatic Powder of Chalk and Opium. Pulvis Ipecacuanhae et Opii B. Dovers Powder. Pulvis Ipecacuanhae Compositus B. Pulvis Kino Compositus B. Compound Kino Powder. Suppositoriae Plumbi cum Opio B. Compound Lead Suppositories. Tablettae Plumbi cum Opio B. Unguentum Gallae cum Opio B. Gali and Opium Ointment. Unguentum Gallae Compositum B. Codeine and its salts are excluded from this list. Declaration of habit-forming drugs 1 The substances specified in the First Schedule hereto are hereby declared to be habit-forming drugs. Drugs Advisory Board 3. Registration of drugs 4. Exemption from registration 5. Records to be kept by manufacturer of drugs 7. Import, export and distribution of drugs 8. Labelling of drugs 9. Recall of drugs Prescription of drugs Dispensing of Schedule 1A and 1B drugs Dispensing of Schedule 1C drugs Dispensing of Schedule 2 drugs Dispensing of drugs by nurses Dispensing, general Emergency supply of drugs Registers and records Clinical trials Appeals Classification of drugs Prescribed habit-forming drugs Drugs Advisory Board 1 In accordance with the provisions of section 5 of the Drugs and Related Substances Act, , there is hereby established a Drugs Advisory Board, hereinafter referred to as 'the Board', for the purposes specified in that section. Registration of drugs 1 An application to register a drug, or for the renewal of such registration, shall be made to the Director in Form 1 in the Schedule hereto and shall be accompanied by a fee of P for a drug which is imported, P for a drug which is partially locally manufactured and P for a drug which is totally locally manufactured. Exemption from registration 1 The following drugs shall be exempted from registration- a any drug manufactured or imported by the Central Medical Stores for specific therapeutic use; b any drug imported through the Central Medical Stores as a donation to the Government or to a Government hospital or to a hospital run by a Mission for use in that hospital; c any drug imported under the authority of the Director, or any person authorised by him, for experimental use in hospitals or for specific therapeutic use or scientific research or tests; d any drug prepared extemporaneously by a pharmacist for use as prescribed by a medical practitioner; e any non-scheduled herb used for traditional medicine and exempted by the Director; f any preparation not containing active ingredients in excess of one millionth part of the preparation's own weight. Records to be kept by manufacturer of drugs 1 A manufacturer of drugs shall keep and maintain and hold readily available for inspection, comprehensive records containing details of- a all steps taken in the storage and testing of raw materials; b all steps taken in the manufacture of each batch of drugs; c all tests carried out on representative samples; and d the sale and distribution of each batch of drugs. Import, export and distribution of drugs 1 Importers, exporters and distributors of drugs and for the purpose of this regulation 'distributor' includes wholesaler and retailer, and 'distribution' shall be construed accordingly shall keep and maintain records containing all details of the importation, wholesale and distribution of drugs by them, and such records shall be retained and kept available for inspection by a police officer, or by any person so authorised therefor by the Director for a period of at least five years from the date of each relevant entry. Labelling of drugs 1 The container of every drug imported, manufactured, processed or packed in Botswana shall bear a label written in English, with the following information clearly indicated thereon- a either the approved name of the drug as used in official pharmacopoeias or formularies, or the international non-proprietary name; b the brand name, if any; c the contents of the container; d the quantity of active ingredients per dosage unit; e the name of the manufacturer; f the batch identification; g the expiry date; h any special storage conditions that may be necessary or desirable; i any warnings or precautions that may be necessary or desirable; j any directions for use if sold without prescription; and k any appropriate statutory or restrictive direction or label in the Schedule that may be necessary. Asthmatics should consult their doctor before using this product. May cause drowsiness. If affected do not drive or operate machinery. Avoid alcoholic drink. Do not exceed the stated dose. Recall of drugs Whenever the Director finds that any portion of any batch of drugs does not conform to the standards of identity, strength, quality and purity, or any other requirement specified in the documentation for registration, he may instruct the licensee to discontinue the sale of the remainder of the batch and, so far as is practicable, to recall any portion of the batch already sold. Prescription of drugs 1 Prescriptions of drugs shall be written in generic or approved international non-proprietary names INN except when a particular brand of drug is preferred and clinically acceptable reasons for such preference are communicated to the dispenser. Dispensing of Schedule 1A and 1B drugs 1 Schedule 1A and 1B drugs may only be dispensed or sold by a pharmacist upon a written prescription, by a medical practitioner or dentist, presented for dispensing within thirty days of the date of its issue, and for the supply of a quantity not greater than is indicated on the prescription, which shall not in any case exceed thirty days supply, and any such prescription shall be retained in the pharmacy for a period of three years after the date of dispensing. Dispensing of Schedule 2 drugs Schedule 2 drugs may be dispensed- a in referral hospitals, district hospitals, mission hospitals, mine hospitals or private hospitals by a pharmacist or an intern pharmacist, or by a pharmacy technician under the supervision of a pharmacist, and upon a written prescription issued by a medical practitioner or a dentist; b in a retail pharmacy by a pharmacist, or by a pharmacy technician under the supervision of a pharmacist, and upon a written prescription issued by a medical practitioner or a dentist; or c in a private medical practice or surgery or a Government primary hospital, by a pharmacy technician upon a written prescription issued by a medical practitioner or a medical officer. Dispensing of drugs by nurses Notwithstanding regulations 11, 12 and 13, registered and enrolled nurses in referral, district, primary, mine, mission and private hospitals, clinics, health posts and mobile clinics, may, in the exercise of their duties, dispense Schedule 1A, 1B, 1C, 2 and 3 drugs to patients, upon written prescription by a medical practitioner or a dentist. Dispensing general 1 The dispenser of any drug shall not dispense a quantity thereof greater than the amount stated in the prescription. Emergency supply of drugs 1 In an emergency a Schedule 2 drug can be supplied or dispensed as provided in regulation 13, but without a prescription if- a there is an immediate need for the drug requested to be supplied and it is impracticable in the circumstances to obtain a prescription; or b the treatment with the drug has on a previous occasion been prescribed for the person requesting it. Clinical trials 1 Clinical trials of drugs means studies in humans or animals in order to systematically generate new or verify existing information about their efficacy and their side effects, and also studies relating to their absorption in, metabolism and excretion from the human or animal body. Appeals Any appeal lodged in accordance with the provisions of section 14 of the Act or regulation 18 6 shall be lodged within thirty days after the date when the decision appealed against is communicated to the applicant. Classification of drugs For the purposes of the Act and these Regulations drugs shall be classified in accordance with the lists set out in the First Schedule. Prescribed habit-forming drugs For the purposes of the definition of 'habit-forming drug', section 3 1 b and Part III of the Act the drugs listed in the Second Schedule are declared to be banned habit-forming drugs. Forms The forms to be used for the purposes of the Act shall be in accordance with the forms set out in the Third Schedule. Cereoli Iodoformi et Morphinae B.
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Cannabis Use Disorder Among First-Year Undergraduate Students in Gaborone, Botswana
Gaborone where can I buy cocaine
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Cannabis Use Disorder Among First-Year Undergraduate Students in Gaborone, Botswana
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