Newborn Birth Defect Screening Kit Development Service

Alta DiagenoTech is an authority on in vitro diagnostic (IVD) products and services with a specialization in newborn birth defects screening. We focus on offering precise and effective testing solutions for medical institutions and laboratories. The newborn screening test kits we developed make use of an advanced technology platform to rapidly and accurately detect a wide range of congenital anomalies, which aids in early diagnosis, early intervention, and improving the health of newborns.

Choose Alta as Your Professional Partner in Diagnostics

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Our kits are developed using tools such as mass spectrometry (LC-MS/MS) or fluorescence analysis, which have the advantages of high sensitivity, high specificity, and automation. These techniques can be used with different types of newborn heel blood dried blood film samples for wide-scale screening. Trustworthy reports can be produced swiftly alongside the intelligent analysis software to streamline technique diagnosis and intervention, which in turn, lowers the chance of birth defect disabilities.

Newborn Birth Defect Screening Kit Development

We are able to develop neonatal screening kits for birth defects, including but not limited to:

Blood vessel microscopic view with red blood cells, blue abnormal cells, large rough-surfaced tumor-like cells causing inflammation.

Inherited Metabolic Disorders (IEMs) Diagnostic Kit

Congenital hypothyroidism (CH)
Glucose-6-phosphate dehydrogenase deficiency (serotonin)
Congenital adrenocortical hyperplasia (CAH)
Galactosemia

Knee joint internal anatomy with bones, joint fluid, and cellular activity related to arthritis, for medical diagnostics.

Amino Acid Metabolism Disorders Diagnostic Kit

Phenylketonuria (PKU)
Maple sugar urine disease (MSUD)
Homocystinuria (HCU)

Red blood cells with molecular structures between them, showing drug-cell interaction.

Neuromuscular Diseases Diagnostic Kit

Spinal muscular atrophy (SMA)
Duchenne muscular dystrophy (DMD)

Purple X-shaped chromosomes in blue fluid, for genetic analysis.

Fatty Acid Oxidation Metabolism and Organic Acid Metabolism Disorder Detection Kit

Medium chain acyl coenzyme A dehydrogenase deficiency (MCAD)
Methylmalonic acidemia (MMA)
Propionic acidemia (PA)

Lab scene with multiple test tube racks, tubes with colored liquids, gloved hands handling samples.

Other Extended Screening Programs

Hereditary deafness
Thalassemia
X-linked adrenoleukodystrophy (X-ALD)
Adenosine deaminase deficiency (ADA-SCID)

Development Process

Newborn birth defect screening kit development service process.

About Us

Our highly expert and experienced senior engineers and researchers integrate their extensive practical experience with deep theoretical knowledge to understand precisely the latest trends shaping the industry. Equally, we offer a complete level of assistance from consulting and solution tailoring through troubleshooting that works towards the enhancement of the health of neonates.

Alta DiagnoTech integrates with the information technology management platform to offer clients comprehensive services from development validation to production in a single service. To ensure clients the highest efficiency and reliability, we optimize product structures, enhance accuracy, reduce cost, and provide advanced services through diagnostics. If you are interested in our services, please feel free to contact us for more information.