Toggle Offcanvas
...
Global Government Tenders

Most trusted source for Tendering Opportunities and Business Intelligence since 2002

Within The Framework Of The State Program Of Maternal And Child Health, The Purchase Of Medical Services Related To Neonatal And Children'S Hypothyroidism, Phenylketonia, Hyperfenylalanineemia, Mucoviscidosis, Galactosemia, Adrenogenital Syndrome And Biotinidase Deficiency.

სსიპ ჯანმრთელობის ეროვნული სააგენტო Georgia has Released a tender for Within The Framework Of The State Program Of Maternal And Child Health, The Purchase Of Medical Services Related To Neonatal And Children'S Hypothyroidism, Phenylketonia, Hyperfenylalanineemia, Mucoviscidosis, Galactosemia, Adrenogenital Syndrome And Biotinidase Deficiency. in Healthcare Equipment and Services. The tender was released on May 17, 2025.

Country - Georgia

Summary - Within The Framework Of The State Program Of Maternal And Child Health, The Purchase Of Medical Services Related To Neonatal And Children'S Hypothyroidism, Phenylketonia, Hyperfenylalanineemia, Mucoviscidosis, Galactosemia, Adrenogenital Syndrome And Biotinidase Deficiency.

Deadline - Jun 16, 2025

GT reference number - 109086029

Product classification - Services provided by medical laboratories

Organization Details:

  Address - Georgia

  Contact details - 565656565

  Tender notice no. - 76454545

  GT Ref Id - 109086029

  Document Type - Tender Notices

Notice Details and Documents:

Description - Description: 1.2.1. The purpose of the purchase is to identify early identification of diseases in infants/children whose timely detection and treatment will reduce newborn mortality and the development of permanent disability. Service benefits will be newborns and children throughout Georgia.1.2.2. The tender winner should ensure:1.2.2.1. Detection of neonates on hypothyroidism, phenylketonuria, hyperfenylalanineemia and mucoviscidosis through the screening of all newborns born nationwide;1.2.2.2. Secondary diagnosis of infants with phenylketonuria and hyperphenylalanineemia to confirm the disease;1.2.2.3. Consulting families bearing families of abnormal genes of phenylketonuria and hyperfe

Gt Ref Id - 109086029

Deadline - Jun 16, 2025

Share share

Similar Tenders :

Summary:
Create Account

Why Us

3,00,000 +

Users

190 +

Countries Covered

5,00,000 +

Agencies Tracked

50,000 +

Notices Daily

90 Million +

Database