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World Health Organization. Kingdom Of Morocco Ministry Of Health. ICIUM Third International Conference for Improving use of Medicines. Measuring Transparency in the Moroccan Public Pharmaceutical Sector . 14 -18 NOVEMBER 2011 – ANTALYA TURKEY. Dr. Mohamed Laghdaf RHAOUTI
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World Health Organization Kingdom Of Morocco Ministry Of Health ICIUM Third International Conference for Improving use of Medicines Measuring Transparencyin the Moroccan Public Pharmaceutical Sector 14 -18 NOVEMBER 2011 – ANTALYA TURKEY Dr. Mohamed Laghdaf RHAOUTI National assessor – Morocco
General data Private sector : • The 2nd industry of drugs in the African continent; • 32 manufacturing units in conformity with the international standards; • 70% of the requirements provided by the local production; • More than 5000 specialties; • 10% of the production intended for export; • Good provisioning is ensured by a network of about 50 wholesalers and more than 9000 pharmacies. Public sector : • 10% of the consumption of drugs in value, is not producer of drugs; • Approximately 160 pharmacists; • A national laboratory of control : • Accredited by the European Directorate of Quality of Medicines(EDQM) according to the Standard ISO 17025. • Associate member of the European Pharmacopeia. • Member of the European Network of official laboratories of medicines’ control;
General findings The vulnerability assessment to corruption for the 8 functions of our study is summarized as follows : • - The vulnerability to corruption is marginal for 4 functions : registration, licensing, procurement and distribution, they constitute half of the functions studied. • - The vulnerability is moderate for 2 functions: inspection and clinical trials, they constitute a quarter of the 8 functions. • - On the other hand, this vulnerability is high for 2 functions: promotion and selection, they constitute a quarter of the 8 functions.
KIs • 55 KIs • Most of them answered several questionnaires at the same time; • Almost 300 questionnaires were answered, i.e. :30 KIsper function on average, higher than necessary;
Registration : Strengths (Marginal Vulnerability) Existence of : • A specific legislative and regulatory frame; • A National Laboratory of Control operational and accredited by EDQM; • A Committee of ratification which meets regularly and keeps minutes of its meetings; • A list of all the pharmaceutical products and an information system for the registration process; • Written procedures accessible to the public on the way of presenting and evaluating the requests of registration of medicines.
Registraration : Weaknesses (Marginal Vulnerability) Absence of : • A written document • requiring a statement of (COI); • clarifying the mandate duration of the committee members; • describing clearly the required professional qualifications, the technical competencies and the practical experience of the members of this committee.
Licensing : Strengths(Marginal Vulnerability) Existence of : • A specific legislative and regulatory frame; • An authorization to start a pharmaceutical establishment is legally necessary; • A sworn inspectors' body of pharmacy, qualified and operational; • A procedure of approval of pharmaceutical establishments in strict conformity with policies and procedures; • An official committee entirely operational and meeting regularly; • Written procedures and guidelines for the evaluation of applications for licenses; • Guidelines on assessment of applications; • An inspection report obligatory prior to the obtention of license; • An up-to-date list of all licensed pharmaceutical establishments.
Licensing : Weaknesses(Marginal Vulnerability) Absence of : • A written document : • requiring a declaration of conflict of interest; • specifying the mandate duration of the committee members, and their role and responsibilities, • A single counter to submit applications for licenses in order to reduce the number of parties involved in the licensing process. • A frame of reference to govern these authorizations especially good manufacturing and distribution practices.
Inspection : Strengths(Moderate Vulnerability) • Existence of : • A provision on the inspection of the pharmaceutical establishments in • the drug regulations; • A sworn, qualified and operational body of inspectors of pharmacy; • Standardized operating procedures (SOPs) written for the inspectors • on how to conduct inspections; • The integrity of the inspectors is not influenced by personal • profits such as gifts, material profits or other favors;
Inspection : Weaknesses(Moderate Vulnerability) Absence of : • A department specific to the inspection of pharmacy within the Directorate of Medicines and Pharmacy (DMP); • A specific set of laws that enable the inspectors to enjoy autonomy of work; • A frame of reference related to the good practices, in particular good manufacturing, distribution and officinal practices; • written guidelines on COI;
Promotion Control : Strengths(High Vulnerability) • Existence of a shy legislation on the promotion of drugs; • Pre-approval of promotion is officially required;
Promotion Control : Weaknesses (High Vulnerability) • Absence of an ethical charter for promotion; • The materials of promotion are not always approved before being • exposed to the public; • The civil society/NGOs do not have an influence on the improvement of • the control of drugs promotion; • Absence of a formal procedure of complaint to denounce unethical • promotional practices; • There exists a service responsible for the monitoring and application of • the provisions concerning drugs promotion but : • the members of this service are not designated on the basis of clear criteria; • there is absence of a written document indicating the composition and the • terms of reference of this service;
Clinical Trials : Strengths (Moderate Vulnerability) • KIs approve that the regulation authority of medicines tries • to ensure that the clinical trials are in accordance with : • The regulations; • The principles of the GCP;
Clinical Trials : Weaknesses (Moderate Vulnerability) • Absence of : • A legislative provision imposing the regulation of clinical trials; • Regulations allowing to set up officially : • A National Ethics Committee with attributions and a multidisciplinary • composition involving(academics, lawyers, scholars, sociologists, civil society,…) • An independent Ethics Committee that operates under the supervision • of the National Committee. • The members of the IEC and of the Review Committee belonging to the • MRA, are not always designated in accordance with the written selection • criteria; • Provisions allowing to specify relations between all parties involved in CT • (IEC members, MRA review committee members, investigators, sponsors, • trial subjects, etc …..)
Selection : Strengths (High Vulnerability) • Existence of : • A List of the Essential Medicines; • A committee responsible to select the medicines that should • be registered in the EML;
Selection : Weaknesses (High Vulnerability) • EML was not established in consultation with all concerned parties and • using an evidence-based approach; • KIs disapprove that the committee responsible for the selection of • national EML is operating under no external influence; • Absence of Clear written guidelines, accessible to the public on the • process of selection of the medicines to be included into, deleted or • rejected from the national EML; • The nomination of the selection committee members is not subject to • clear criteria; • Absence of Guidelines on COI with regard to the selection of essential • medicines; • The role and responsibilities of the selection committee are not • stipulated in their global mission.
Procurement : Strengths (Marginal Vulnerability) Existence of : • Transparent and explicit procurement procedures of pharmaceutical products ; • Written guidance for procurement staff to use according to types of products; • Procurement is made according to an objective method of quantification; • A procurement office and a tender committee with clearly separated functions; • An efficient post-tender system to monitor and report to the tender committee on suppliers’ performance.
Procurement : Weaknesses (Marginal Vulnerability) • The procurement department does not function like an autonomous • structure specialized only in the procurement of medicines and medical • goods; • The requirements in medicines in the public structures are not established • on rigorous scientific foundations and the budgets to meet these needs are • not consequently sufficient; • The process of grouped procurement does not integrate the medicines of • the national medical programs; • Absence of written guidelines on the conflicts of interests.
Distribution : Strengths (Marginal Vulnerability) • Existence of : • A system of customs clearance at the borders; • A system of security management to supervise storage and distribution; • An appropriate form to request medicines; • Appropriate procedures to dispose of expired or spoiled medicines;
Distribution : Weaknesses (Marginal Vulnerability) • The majority of informants do not think that pharmaceutical products are • easily cleared through customs and that it is not necessary to give presents • to speed up the process; • Absence of an assessment and monitoring project of the quality of the • medicines distribution system; • Only ½ of the informants think that leakages in the medicine distribution • system are very rare; • Elaboration of a national project for essential medicines allowing to • level up hospital pharmacies; • Combat the lack of regional pharmacies to bring medicines closer to the • consumer; • Generalize outsourcing of deliveries by private conveyors;
Key Recommendations • On the organizational level: • Organize a national workshop; • Set up a National Piloting Committee; • On the legislative and regulatory level : • Set and publish specific regulations in different domains by taking into account specific • recommendations listed in the report; • On the ethical level : • Require statements of conflict of interest for the members of all committees of different functions • and specify the duration of the mission of these members; • On the level of human resources: • The MRA should recruit, train and motivate a sufficient number of multidisciplinary, qualified • and experimented personnel; • The MOH should sensitize other Ministries and Departments to recruit pharmacists; • On the level of information, education and communication: • Launch a campaign of sensitization; • Make explicit, in written documents accessible to the public, notably via Internet, all • procedures; guidelines, and documents relating to all functions as well as members of committees • and their statements of conflict of interest.