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Poisons Act

Poisons Act

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Published by: jigy-jig on Oct 28, 2009
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 NORTHERN TERRITORY OF AUSTRALIAPOISONS AND DANGEROUS DRUGS
 
ACTAs in force at 16 May 2005TABLE OF PROVISIONSSectionPART I – PRELIMINARY1. Short title2. Commencement3. Repeal4. Savings5. Crown to be bound6. Interpretation6A. Application of SUSDP7. Delegation8. Inspectors9. Powers of inspectors9A.
 
Chief Poisons InspectorPART II – MANUFACTURE OF POISONS10. Definition11. Manufacturer to be registered12. Registration of manufacturer's premises13. Transfer of registration14. Display of certificate of registration15. Cancellation of registration16. Powers of nominated personPART III – CONTROL OF WHOLESALERS17. Wholesaler to be registered18. Application for registration19. Transfer of registration20. Display of certificate21. Cancellation of registration22. Powers of nominated personPART IV – CONTROL OF RETAILERS23. Retailers to be licensed24. Application for licence25. Display of licence
 
 ii 26. Terms and conditions of licence27. Limitation on right of supplyPART V – SUPPLY OF POISONS BY PHARMACISTS, DENTISTS ANDVETERINARIANS28. Supply by pharmacists29. Supply of substances for therapeutic use29A. [Repealed]30. Pharmacist not to hold certain substances31. Prohibition of possession, supply etc. of Schedule 8 substancesPART VA – SUPPLY OF POISONS BY MEDICAL PRACTITIONERS
 Division 1 – Preliminary
31A. Definitions31B. Declaration of restricted Schedule 8 substances
 Division 2 – Supply of poisons generally by medical practitioners
31C. Supply of certain poisons for therapeutic use31D. Supply of restricted Schedule 4 substances31E. Restriction on supply of amphetamines
 Division 3 – Supply of Schedule 8 substances by medical practitioners
31F. Supply of non-restricted Schedule 8 substances31G. Supply of restricted Schedule 8 substances31H. Applications for and granting of authorisations31J. Variation, suspension and revocation of authorisations31K. Supply to be in accordance with authorisation31L. Notification of supply of Schedule 8 substances31M. Medical practitioner's immunity against liability31N. Prohibition of possession, supply etc. of Schedule 8 substances31P.
 
Exemptions from requirement to hold authorisation
 
PART VAA – COMMITTEE AND GUIDELINES
 
31Q. Committee31R. Functions and powers of Committee31S. Meetings of Committee31T. Delegation by Committee31U. Non-disclosure of information by Committee member31V. Protection of members from liability31W. Guidelines31X. Offence to contravene Guidelines
 
 iii PART VI – PRESCRIPTIONS32. Application33. Contents of prescriptions34. Period of effect of prescription and permissible supply35. Endorsement on prescriptions36. Record of prescriptions37. Supply in an emergency38. Possession, &c., of Schedule 8 substancePART VII – HOSPITALS, HEALTH CENTRES ETC.38A. Definitions for Part VII39. Storage, supply and administration in hospitals40. Register of Schedule 8 substances in wards and health centres41. When administration etc. of Schedule 8 substance to bewitnessedPART VIII – MEDICAL KITS42. Authorisation of poisons in medical kits43. Administration from medical kitsPART IX – RECORDS44. Manufacturers to keep records45. Wholesalers to keep records46. Retailers to keep records47. Pharmacists to keep records48. Medical practitioners etc. to keep records49. Authorised persons to keep records50. Retention of recordsPART X – STORAGE OF POISONS51. Storage to prevent public access52. Storage of Schedule 8 substancesPART XI – SCHEDULE 7 SUBSTANCES AND PESTICIDES52A. [Repealed]53. Possession and use of Schedule 7 substances54. Supply of Schedule 7 substances55. Application for licence56. Grant of licence57. Renewal of licence58. Authority of licence

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