tailieunhanh - Health Products Bill - Health Products Act 2007

Where relevant, account should be taken of possible socio-economic impacts of research, including its intended and unintended consequences and the inherent risks and opportunities. A sound understanding of this issue should be demonstrated both at the level of research design and research management. In this context, where appropriate, the projects should ensure engagement of relevant stakeholders (., user groups, civil society organisations, policy-makers) as well as cultivate a multi-disciplinary approach (including, where relevant researchers from social sciences and humanities). Projects raising ethical or security concerns are also encouraged to pay attention to wider public outreach. . | Health Products Bill Bill No. 3 2007. Read the first time on 22nd January 2007. HEALTH PRODUCTS ACT 2007 No. of 2007 ARRANGEMENT OF SECTIONS PART I PRELIMINARY Section 1. Short title and commencement 2. Interpretation 3. Purposes of Act 4. Act to apply only to health products specified in First Schedule 5. Act not to apply to supply or use of health products and active ingredients for veterinary purposes PART II ADMINISTRATION 6. Administration of Act 7. Appointment of enforcement officers 8. Designation of analysts 9. Enforcement officers and analysts deemed to be public officers 10. Advisory Committees 11. Appeal Advisory Committees PART III MANUFACTURE AND IMPORT OF HEALTH PRODUCTS 12. Manufacture of health products 13. Import of health products 11 PART IV SUPPLY OF HEALTH PRODUCTS Section 14. Wholesaling of health products 15. Prohibition against supply of unregistered health products 16. Prohibition against supply of health products that are adulterated counterfeits etc. 17. Supply of health products to be carried out in accordance with prescribed requirements 18. Presentation of health products PART V ADVERTISEMENT OF HEALTH PRODUCTS 19. Advertisement of health products 20. False or misleading advertisement 21. Further requirements for advertisement of health products 22. Defences 23. Corrective measures in relation to contravening advertisements PART VI LICENCES 24. Issue and renewal of licences 25. Variation of licence conditions on application by licensee 26. Register of licensees 27. Suspension and revocation of licence and cancellation of approval 28. Appeal PART VII REGISTRATION OF HEALTH PRODUCTS 29. Health products to be registered according to categories in First Schedule 30. Registration of health products 31. Duration of registration 32. Conditions of registration 33. Evaluation of health products 34. Register of Health Products 35. Re-categorisation or reclassification of health products on application of registrant 36. Power to re-categorise or .