SmartBio Analytics collaborates with preclinical and clinical CROs worldwide to deliver accurate, regulatory-ready and fast-turnaround bioanalytical services. We provide reliable analytical support that helps CROs meet demanding project timelines and regulatory requirements with confidence.
We know that your reputation depends on the quality, reliability, and timeliness of the results you deliver to your sponsors. That’s why we make logistics, communication, and data integrity top priorities in every collaboration.
We collaborate closely with CROs that do not have in-house LC/MS bioanalytical capacity — or that need to extend their capabilities for specific molecules or studies. Whether it’s PK/TK, biodistribution, biomarker quantification, or bioequivalence studies, we ensure seamless integration into your workflows, maintaining full GLP compliance and transparent communication at every stage.
Founders with first-hand CRO backgrounds, understanding your operational realities
Method development in 1–2 weeks, validation in 4–6 weeks, analysis results in ≤ 5 days
Proven processes for secure sample handling, chain of custody, and timely delivery
Regular updates, single points of contact, and responsive support
Full alignment with QA & Certifications requirements for regulatory acceptance
From innovative small molecules to complex biomolecules such as peptides, oligonucleotides, lipids, and proteins
By partnering with SmartBio Analytics, CROs gain a trusted, responsive, and quality-focused bioanalytical ally
— ensuring that your clients receive the data they need, exactly when they need it.
