Our laboratory services

Nordic BioAnalysis AB provides certified analytical and support laboratory services for companies in the pharmaceutical, biotech, medical device and related industries. Our offering includes microbiological and molecular testing, biochemical and chemical analysis, method validation, pharmaceutical stability storage and testing services. Our services are performed under GMP & ISO compliant procedures and can be adapted to meet customer-specific or regulatory requirements.

Microbiological and Molecular Biological Analysis

Microbiological and molecular analytical services supporting product development, contamination control, water system monitoring and cleanroom evaluation. Includes methods such as bioburden testing (TAMC/TYMC), method suitability testing, endotoxin analysis and pharmaceutical water analysis:

Biochemical and Chemical Analysis

Analytical methods for protein characterization, physicochemical testing and impurity analysis. Services include various chromatographic characterization methods such as SEC, IEX and RP-HPLC, as well as electrophoretic techniques like SDS-PAGE, immunoassays including ELISA and Western blot, and elemental analysis to support batch release, identity verification and stability studies.

Pharmaceutical Water Testing

Ensure water system compliance with regulatory and pharmacopeial standards. NWe provides comprehensive testing of Purified Water (PW) and Water for Injection (WFI), including bioburden, endotoxins, TOC, conductivity, heavy metals and more. Our GMP-compliant services support product safety, batch release, equipment qualification and routine monitoring across pharmaceutical production.

QC Release Analysis

Ensure compliant, high-quality product release with Nordic BioAnalysis’ certified QC Release Testing services. We support pharmaceutical and biotech companies with batch-specific testing of raw materials, APIs, and finished products. With validated methods, dedicated lab contacts, and tailored reporting, we help accelerate market access, reduce compliance risk, and uphold patient safety.

Method Development, Validation & Transfer

Support in refining and improving analytical methods across microbiology, biochemistry and chemistry. Services include evaluation of method design, method suitability testing, resolving variability, adaptation to new matrices and validation planning.

Stability Storage and Testing services

Pharmaceutical storage and analysis of pharmaceutical, biotechnological, or chemical products under controlled conditions in qualified chambers aligned with ICH Q1A guidelines to assess how these conditions affect the product’s quality, safety, and efficacy over time. Includes ultra-low, refrigerated and ambient stability storage for short-term and long-term programs with continuous monitoring. We provide dedicated full analytical support for pharmaceutical stability studies—ensuring precise, compliant, and reliable results.

Why choose us

We combine scientific expertise with practical experience in GMP- and ISO-regulated environments to deliver services that are reliable, compliant and responsive to customer needs. Our team includes specialists in analytical chemistry, microbiology, molecular biology and quality systems, and we prioritize accuracy, speed and personalized service in every assignment.

All analyses and processes are conducted according to validated methods, and we work closely with our customers to ensure that regulatory and technical requirements are fully met.

Get in touch

If you’d like to learn more about our laboratory services or explore how we can support your project, feel free to reach out to us at info@norbab.com or +46(0)812154500. We’re happy to provide further details or prepare a tailored proposal based on your specific needs.