Radioisotope and Radiopharmaceutical Production and Irradiation Services
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The Presidency of NÜKEN is responsible for fulfilling service requests listed in the “TENMAK Service and Transaction Fees” within its own capabilities. External suppliers are not used to fulfil services requested by customers. Customers request a service by approving the service-specific Contract during the application process via e-Government (https://ehizmet.tenmak.gov.tr). For e-Government applications, payment is made against the automatic assessment generated after the request; for certain services where this is not possible, payment is made against the assessment issued by the Presidency of NÜKEN after the request is received. The Presidency of NÜKEN is not responsible for collecting the sample/device/product.
Information on how the sample/device/product is to be sent and on the service duration is displayed as a “Service Information Document” for each service during the e-Government application process. Any sample/device/product delivered to the Presidency of NÜKEN is deemed to have been submitted under appropriate conditions and in the manner specified in the “Service Information Document”.
Unless otherwise stated, the Presidency of NÜKEN provides the requested services in accordance with standards accepted by national and international organisations, guidance documents having the status of standards, or, where these are unavailable, the technical documentation and operating manuals supplied by the device/system manufacturers. If the method requested by the customer is considered unsuitable or out of date, the customer is informed.
To help us improve the quality of the service you have received, we kindly ask you to complete our Survey (Customer Satisfaction, Suggestions and Complaints Form). Thank you for your attention and cooperation.
Interested Party Complaint, Suggestion and Survey Procedure
For invoices: Presidency of TENMAK: 0312-2958728-29, gelirlersubesi@tenmak.gov.tr
No. | Service Code | Service Name |
|---|---|---|
1 | 08.01.01.00.00 | Transfer of a Radioactive Source |
2 | 08.01.01.00.00 | Transfer of a Radioactive Source |
3 | 08.01.02.00.00 | Radioactive Standard Point Source (137Cs, 60Co, 152Eu; activity range 1-10 kBq) |
4 | 08.01.02.00.00 | Radioactive Standard Point Source (137Cs, 60Co, 152Eu; activity range 1-10 kBq) (CANCELLED because no quotation was received) |
5 | 08.01.03.00.00 | TAEK-RM-1 Tea Radioactive Standard Reference Material (100 g) |
6 | 08.02.01.01.00 | Irradiation with a Dose up to 10 kGy |
7 | 08.02.01.02.00 | Irradiation with a Dose above 10 kGy |
8 | 08.02.01.03.01 | Product-specific Dose Mapping Study |
9 | 08.02.01.03.02 | Irradiations at Special Dose Rates |
10 | 08.02.02.00.00 | For Irradiations Performed in the Gamma Cell (for irradiations below 1 kGy, a fee equivalent to 1 kGy is charged per sample) |
11 | 08.02.03.00.00 | Irradiation with a Neutron Beam |
12 | 08.02.04.00.00 | Determination of Gamma Linear Attenuation Coefficients of Materials |
13 | 08.02.05.00.00 | Proton-beam Irradiation for R&D Purposes |
14 | 08.02.06.01.01 | Sterility Testing of Medical Devices (Direct Inoculation) - For Medical Purposes (10 samples) |
15 | 08.02.06.01.02 | Sterility Testing of Medical Devices (Direct Inoculation) - For Validation Purposes (100 samples) |
16 | 08.02.06.02.00 | Determination of the Microbial Population (Bioburden) of Medical Devices |
17 | 08.02.06.03.01 | Determination of the Radiation Sterilisation Dose for Medical Devices: Dose Selection Test - Method 1 (Single Lot) |
18 | 08.02.06.03.02 | Determination of the Radiation Sterilisation Dose for Medical Devices: Dose Selection Test - Method 1 (Three Lots) |
19 | 08.02.06.03.03 | Determination of the Radiation Sterilisation Dose for Medical Devices: Dose Selection Test - Method 2 (Three Lots) |
20 | 08.02.06.03.04 | Determination of the Radiation Sterilisation Dose for Medical Devices: Dose Validation Test - Vdmax 25&15 (Single Lot) |
21 | 08.02.06.03.05 | Determination of the Radiation Sterilisation Dose for Medical Devices: Dose Validation Test - Vdmax 25&15 (Three Lots) |
22 | 08.02.06.03.06 | Determination of the Radiation Sterilisation Dose for Medical Devices: Dose Audit Test - Vdmax 25&15 (Single Lot) |
23 | 08.02.06.03.07 | Determination of the Radiation Sterilisation Dose for Medical Devices: Dose Audit Test - Method 1 (Single Lot) |
24 | 08.03.01.00.00 | TAEK-PHT 123I-NaI (Sodium Iodide) 75 mCi/mL Active Substance * |
25 | 08.03.02.00.00 | TAEK-PHT 18F-FDG (Fluorodeoxyglucose) 740-11100 MBq/mL Vial Containing Solution for Injection** |
26 | 08.03.03.00.00 | TAEK-PHT 123 I-NaI (Sodium Iodide) 37 MBq/mL Vial Containing Solution for Injection*** |
27 | 08.03.04.00.00 | TAEK-PHT 201 TlCl (Thallium Chloride) 37 MBq/mL Solution for Injection**** |
28 | 08.03.05.00.00 | TAEK-PHT F-18 (Fluorine-18) Active Substance ***** |
29 | 08.03.06.00.00 | TAEK-PHT Tl-201 (Thallium-201) Active Substance****** |
30 | 08.03.07.00.00 | TAEK-PHT 123 I-NaI (Sodium Iodide) 75 mCi/mL Active Substance******* |
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NUCLEAR ENERGY RESEARCH INSTITUTE - Ankara Campus:
This page updated at 22 September 2026 13:44
