HUS 080-2024 Genetic testing for rare diseases, various methods
Awarded
The competition has ended and a winner has been selected.
Helse- og sosial tjenesteyting
HUS-yhtymä has entered into an agreement with Centogene GmbH and MVZ Martinsried GmbH for genetic testing for rare diseases using various methods. The services include 20 different genetic tests, such as Ataxia repeat analysis, repeat expansion analysis, genetic testing for hereditary Alpha Tryptasemia, MLH1 promoter methylation analysis, Beckwith-Wiedemann syndrome testing, Cystic fibrosis (CF-EU2), Long-range PCR analysis of CYP21A2, PKD1, PKD2, PMS2, SBDS, genetic testing for facioscapulohumeral muscular dystrophy (FSHD1 and FSHD2), Chromosomal breakage test (Fanconi anemia), Relative telomere length analysis, X inactivation test, genetic testing for haemoglobinopathies, Germline episignature, DNA methylation pattern testing for specific genetic disorders, Sanger sequencing/ Long-range PCR analysis of the VWF gene, and Retinoblastoma genetic screening. The total value of the contract is 1,100,000 €. Two bids were received for this procurement.
Result
- Winners
- CENTOGENE GmbH
- MVZ Martinsried GmbH
- Number of bids
- 2
- Contract value
- €1,100,000
About the bid
- Contact name
- Arttu Karjalainen
- Contact phone
- +358 503549873
- Contact email
- mons.vermis@gmail.com
- Address
- Uutistie 5, 01770 Vantaa
The Procurement Entities HUS Group (later also ”HUS”) and ISLAB requested tenders for genetic testing for rare diseases using various methods. The procurement included the following tests: 1. Ataxia repeat analysis by NGS 2. Repeat expansion analysis (UGT1A1) 3. Repeat expansion analysis (CANVAS) 4. Repeat expansion analysis (MUC1) 5. Genetic testing for hereditary Alpha Tryptasemia 6. MLH1 promoter methylation analysis 7. Beckwith-Wiedemann syndrome testing 8. Cystic fibrosis (CF-EU2) 9. Long-range PCR analysis of CYP21A2 10. Long-range PCR analysis of PKD1 and PKD2 11. Long-range PCR analysis of PMS2 12. Long-range PCR analysis of SBDS 13. Genetic testing for facioscapulohumeral muscular dystrophy (FSHD1 and FSHD2) 14. Chromosomal breakage test (Fanconi anemia) 15. Relative telomere length analysis 16. X inactivation test 17. Genetic testing for haemoglobinopathies 18. Germline episignature, DNA methylation pattern testing for specific genetic disorders 19. Sanger sequencing/ Long-range PCR analysis of the VWF gene 20. Retinoblastoma genetic screening. The procurement was divided into lots so that each test was an independent part of the procurement. An agreement was made with each selected service provider, which included the services for which the service provider had been selected as the supplier.Main features of the procedureThe procurement procedure is an open procedure in accordance with Section 109 of the Finnish Act on Public Procurement and Concession Contracts (1397/2016, "Procurement Act"), where any tenderer can participate in. Section 96 of the Procurement Act regarding abnormally low tenders applies to this procurement. The procedure is as follows: Procurement Entity will: 1. open tenders 2. verify answers given to the suitability requirements 3. verify tender's compliance with call for tenders After that, the Procurement Entity may 4A. conduct a tender comparison, or 4B. proceed to the negotiation procedure. The negotiation procedure may be proceeded to if: A. no tenders have been received in the tender in accordance with the call for tenders; B. no tenders can be accepted due to too high a price or other reason; or C. the Procurement Entity deems it necessary to negotiate the details of the tenders. The Procurement Entity may decide to proceed to the negotiation procedure with one, several or all sub-areas of the procurement. In other sub-areas the comparison of tenders is conducted on the base of the original tenders. All tenderers who have submitted a tender by the deadline and who meet the conditions regarding the suitability of the tenderer described in this call for tenders will be invited to the negotiations. The aim of the negotiations is to update the original call for tenders so that the tenderers selected for the negotiations can submit new tenders based on it. The negotiations will be conducted equally with all invited tenderers for a period determined by the Procurement Entity. After the negotiations, the Procurement Entity will submit an updated call for tenders to all tenderers who participated in the negotiations, on the basis of which the tenderers will submit new tenders. After this, the procurement procedure continues from point 1 described above based on the new call for tenders. After the tender comparison has been conducted, the Procurement Entity will: 5. request the winning tenderers to submit reports and other documents related to the suitability requirements 6. make a procurement decision 8. sign agreements with the chosen tenderers.
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Award Criteria
Description
Comparison price is the price of the analysis.
Description
If the test is accredited, the tenderer will receive the maximum score (40 points) in quality comparison of this sub-area. If the test is not accredited, the tenderer will receive zero (0) points.
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See the full notice
- Contracting authority
- HUS-yhtymä
- Title
- HUS 080-2024 Genetic testing for rare diseases, various methods
- Type
- Main code
- Supplemental codes
No supplemental codes from buyer…