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IV          โครงการสังเคราะห์ข้อเสนอ
                           เพื่อเสริมสร้างการอภิบาลระบบยา




                            medicines, (5) The constraints from budget for operation in Thai-FDA and

                            remuneration for personnel, (6) The discontinuity of medicinal license reviews
                            and (7) The lack of technology promotion and medicinal laboratory for

                            medicinal verification
                         2. The risk of Drug Selections consists of (1)  The appointment and operation

                            of the National Drug System Development Committee, (2) The role and conflict
                            between working group on special experts and working group on Health

                            Economics, (3) The conflict of Interests of the members of committee,
                            sub-committees and working groups, (4) The relation between pharmaceutical

                            industries and the National Drug System Development Committee, (5) The lack
                            of accountable identification to committee and (6) The principles and
                            regulation for Drug Efficiency and Cost-effectiveness of drug

                         3. The risk of Public Procurement for medicines consists of (1) The lack of

                            drug promotion controls (2) The lack of ethical controls to the members of
                            Pharmacy and Therapeutic Committee (PTC) and health personnel, (3) the

                            standards and regulations of hospitals, (4) the public procurement regulation,
                            and (5) the drug cost estimate determinations



                         The study discovers a various risk in Pharmaceutical Governance in Thailand

                   therefore the study suggests the policy recommendation for the purpose of
                   strengthening and improvement for Pharmaceutical Governance in six principles, consists

                   of (1) the direction of National Drug Policy determination must defines apparently;
                   (2) the all Acts, Regulations and Policies concerned with Pharmaceutical Governance
                   must be improved well-timed and consults by participatory with all stakeholders; (3) the

                   organizations and committees in Pharmaceutical Governance must make clear their roles
                   and improves a professionalisms in accordance with National Drug Policy; (4) The

                   information and communications technology (ICT) in Pharmaceutical Governance have to
                   connects the insignificant and up-to-date information; (5) The professional ethics of all
                   stakeholders have to promote continuously; and (6) Internal and External Audits must

                   be developed and strengthened.
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