Bilgehan Karadayı Turkish MoH
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1 Bilgehan Karadayı Turkish MoH
2 Ministry of Health of Turkey General Directorate of Pharmaceuticals and Pharmacy Social Security Agency Turkish Practice on Medical Device UDI Bilgehan Karadayı, MD Head of Medical Device Department
3 Ministry of Health of Turkey General Directorate of Pharmaceuticals and Pharmacy Turkish Practice on Medical Device UDI Introduction Social Security Agency Turkish Medical Device legislation is translation and adoption of related EU legislation (93/42, 98/79, 90/385). Turkey has a customs union with EU. Turkey can designate Notified Bodies. Turkish manufacturers do not need to have authorized representatives in EU; Turkey can be chosen as the local site for ARs for EU market. 3
4 Ministry of Health of Turkey General Directorate of Pharmaceuticals and Pharmacy Turkish Practice on Medical Device UDI Social Security Agency Total Land : 783,562 km 2 (37th) 2010 census : 73,722,988 (18th) GDP (PPP) : $ billion (16th) : $13,464 per capita Total Expenditure on Health Per Capita $~600 USD(2010) 4
5 Ministry of Health of Turkey General Directorate of Pharmaceuticals and Pharmacy Turkish Practice on Medical Device UDI Introduction Social Security Agency Turkish medical device market is ~2.5-3 billion /per year purchase. The majority of the market (%80) is occupied by imported products. Majority of the health expenditure (%80) is funded by public resources (public insurance). %16 of the registered products by number in the Turkish Medical Device Databank is in the positive (reimbursement) list of SGK. 5
6 Ministry of Health of Turkey General Directorate of Pharmaceuticals and Pharmacy Turkish Practice on Medical Device UDI Social Security Agency Turkish Drug and Medical Device National Databank TITUBB (Türkiye İlaç ve Tıbbi Cihaz Ulusal Bilgi Bankası) Online registration system for medical devices, manufacturers, importers and distributors Operation date 2006 Used also by Social Security Agency (fifty/fifty) for reimbursement procedures. Will be used as the e-catalog for electronic public procurement/tenders (EKAP ; Electronic Public Purchase Platform) 6
7 VENDOR TITUBB E-CATALOGUE REGISTRY PROCESS PRODUCT LEGAL COMMERCE TRANSACTIONS Trade Name Company Profile Location Category User Authetication Commercial Registers Legal Commercial Certificates
8 VENDOR TITUBB E-CATALOGUE REGISTRY PROCESS PRODUCT LEGAL COMMERCE TRANSACTIONS Unique Identification Universal Product No. UNSPSC ontology based classification UNSPSC Class Nomenclature Medical Branch Codes GMDN Categorization Smart syndication of best match equivalents Ontological harmonization One at a life time registration Public Accredation
9 VENDOR TITUBB E-CATALOGUE REGISTRY PROCESS PRODUCT LEGAL COMMERCE TRANSACTIONS Package Tracking Source and Destination Tracking GTIP No. Tracebility Age Sensitivity Control Packaging Data Packaging Quantity
10 VENDOR TITUBB E-CATALOGUE REGISTRY PROCESS PRODUCT LEGAL COMMERCE TRANSACTIONS Online Approval Status Check Reimbursement Rules Mapping Online Current Retail, Wholesale Price Entry Price Effectivity Dates
11 VENDOR TITUBB E-CATALOGUE REGISTRY PROCESS PRODUCT LEGAL COMMERCE TRANSACTIONS Electronically Signed Legal Document Uploads EC Certificates FDA Certificates ISO Certificates Compliance Legislation Declaration of Conformity Calibration Status User Manuals Technical Specification Validity Check Effectivity Check Warning Notices to Vendors
12 VENDOR TITUBB E-CATALOGUE REGISTRY PROCESS PRODUCT LEGAL COMMERCE TRANSACTIONS
13 VENDOR TITUBB E-CATALOGUE REGISTRY PROCESS PRODUCT LEGAL COMMERCE TRANSACTIONS Dealer Registration Mapping Manufacturer and Dealers Monitoring Authorized Dealers Online declaration of territorial exclusivities Monitoring Fake or Banned Dealers Monitoring geographical distribution of actors Monitoring of dealer performance
14 TITUBB E-CATALOGUE REGISTRY PROCESS VENDOR PRODUCT LEGAL COMMERCE TRANSACTIONS Collabration Portal between public authorities OLAP over market formation and activity Vendor Statistics Product Statistics Buyer Statistics UPN based search engine Web services to other e-government suites like customs, tax authority
15 Ministry of Health of Turkey General Directorate of Pharmaceuticals and Pharmacy Turkish Practice on Medical Device UDI Social Security Agency Turkish Drug and Medical Device National Databank TITUBB (Türkiye İlaç ve Tıbbi Cihaz Ulusal Bilgi Bankası) Public health services are obliged to ask for registration to purchase a medical device and, Social Security Agency do not reimburse products unless registered and have a GTIN(EAN ) or HIBC. So every single/unique product must have an identification number GMDN codes declared by the user, is also compulsory to finish the registration 15
16 Ministry of Health of Turkey General Directorate of Pharmaceuticals and Pharmacy Turkish Practice on Medical Device UDI Social Security Agency Turkish Drug and Medical Device National Databank TITUBB (Türkiye İlaç ve Tıbbi Cihaz Ulusal Bilgi Bankası) Registration necessity of every single medical device in TITUBB, is the basis of UDI practice of Turkey And Reimbursement requirements is the main initiative for UDI use in Turkey Social Security Agency uses an electronic system for practical reasons during paying for the medical devices and also wants to fight against counterfeit products. 16
17 Ministry of Health of Turkey General Directorate of Pharmaceuticals and Pharmacy Turkish Practice on Medical Device UDI Social Security Agency Turkish Drug and Medical Device National Databank TITUBB (Türkiye İlaç ve Tıbbi Cihaz Ulusal Bilgi Bankası) MKYS (Malzeme Kaynak Yönetim Sistemi -Product Management System) is the online stock management system used by the public hospitals; it is integrated with TITUBB MEDULA (Medikal Ulak -Medical IT System-) is the online insurance and health service provision system and it is also integrated with TITUBB 17
18 TITUBB STAKEHOLDERS
19 Ministry of Health of Turkey General Directorate of Pharmaceuticals and Pharmacy Turkish Practice on Medical Device UDI Social Security Agency Turkish Perspectives on UDI UDI obligation initiated for the reimbursed products but we felt it is something needed in the medical device management system overall; Market surveillance Vigilance Efficient health service We do not discuss if it is needed or not How and when? 19
20 Ministry of Health of Turkey General Directorate of Pharmaceuticals and Pharmacy Turkish Practice on Medical Device UDI Social Security Agency Conclusion 1.8 million MDs has been registered untill now in TITUBB At the beginning %20 of MDs had original UDI number but nowadays %90 of MDs have original UDI number We do not want conflicts with EU in terms of requirements for putting into market and conformity assessment of MDs but; reimbursement power will continue to speak We can manage the life cycle of a medical device in many steps The End 20
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