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Our job: checking what’s inside before it hits the market

Life Sciences

We are committed to driving innovation in pharmaceuticals and medical devices through rigorous research, diagnostics, and expert regulatory support

Our Life Science division specializes in clinical studies, design development, quality assurance, data management, eCRF solutions, medical writing, and quality control samples. With a deep understanding of industry requirements, we serve pharmaceutical companies, CROs, medical manufacturers, and the scientific community, ensuring compliance with global standards.  

Our expertise is grounded in international regulatory frameworks, including EU, FDA, and ICH guidelines, as well as national authorities such as ANVISA, TGA, and PMDA. 

When it comes to reliability, you can rely on us

CERTANIA is your reliable partner for testing, inspection and certification

Our Life Sciences service segment specializes in research across pharmaceuticals, medical devices, and health diagnostics. The CERTANIA Group rigorously adheres to scientific best practices, consistently meeting international standards and regulatory requirements.

CERTANIA
ClinicalResearch

Clinical research from early development to approval: clinical studies phase I-IV, data management, biometrics, pharmacokinetics and regulatory compliant IT and data solutions for reliable study results.

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HealthcareLabs

Pharmaceutical analysis, hygiene and quality management as well as laboratory diagnostics: stability tests, GMP-compliant tests, audits and quality control materials for safe, effective and reliable healthcare products.

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CERTANIA
MedTech

Testing, engineering and consulting services for medical and pharmaceutical products: Laboratory, biocompatibility and implant testing, validation and regulatory support for safe, international approvals.

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