CONVALENCE LABS

Legally established 2026 · Spain, European Union

Independent testing you can verify, not just trust

Convalence Labs is a newly established independent laboratory, opened in 2026. Built by senior analysts with over 15 years of combined experience in qualitative and quantitative molecular identification. We exist to audit the real composition, purity, and exact dosage of peptides, proteins, and advanced active ingredients, with every sample tested against certified reference standards, and every certificate independently verifiable online.

We collaborate with researchers, athletes, and industry professionals to provide detailed insight into what a sample actually contains, not what its label claims. Being new gives us no legacy client relationships or supplier ties to protect: our only business is testing, so every result stands on its own.

Confidentiality

Confidential, anonymised test reports: your identity and submission details stay private.

Precision & accuracy

Orthogonal GC-MS, NMR, and HPLC methods, cross-checked against certified reference standards.

Integrity & independence

We test only, with no formulation, manufacturing, or sales, so results carry no conflict of interest.

EU-wide coverage

Serving clients across the European Union, with digital certificates verifiable from anywhere.

A logistics network built for the secure transport of chemical compounds lets us process analytical requests from clients located within the European Union. We specialize in the thorough characterization of complex chemical matrices, including pharmaceuticals, peptides, and sports-related additives, while supporting both private individuals and product-development companies. In line with legal counsel, we do not accept opioids or other internationally controlled narcotics for analysis. Every analysis ends with a hash-verified digital report, instantly verifiable by any third party through our public platform.

Javier Montesinos

Lead Analytical Chemist

Holds an official Master's Degree in Analytical Chemistry from the University of Barcelona (UB). Specializes in advanced chromatographic coupling methodologies and the characterization of complex lipophilic matrices via GC-MS. 9 years directing high-throughput purity audits and analytical method validations for regulated testing environments.

Arthur van der Meer, MSc

Senior Method Development Specialist

Graduated from the MSc in Chemical Engineering program at the University of Groningen (RUG), focusing on Advanced Product Engineering. Expertise centers on the design, optimization, and scale-up of HPLC/UHPLC protocols for strict dosage quantification and trace impurity isolation. 6 years supervising manufacturing quality control under European GMP compliance standards.

Matteo Bianchi, MSc

Head of Mass Spectrometry & QA

Completed the international Master's in Advanced Spectroscopy in Chemistry (ASC) at the University of Bologna (Unibo). Specializes in structural confirmation and diagnostic chemical problem-solving using High-Resolution Mass Spectrometry (HRMS). 5-year track record as Quality Assurance and Technical Manager, validating batch homogeneity in certified chemical testing laboratories.