KV LAB d.o.o. (registered as KVOTLAN LABORATORIJ, patentiranje farmacevtskih izdelkov d.o.o., Registration Number: 6392768000) is located at Grintovška ulica 25, 4000 Kranj, Slovenia. Established in 2013, we bring over 13 years of specialized pharmaceutical research experience and operate in strict compliance with European Union and Slovenian laboratory standards.

Corporate leadership is directed by Pavel Glazkov, who serves as Director overseeing strategic pharmaceutical partnerships, laboratory operations, and regulatory alignment. Commercial, administrative, and legal representation is managed by Procurator Jolanda Černivec Pipan, ensuring seamless corporate governance and contractual integrity.

Confidentiality is the cornerstone of our research engagements. Prior to receiving proprietary specifications, chemical samples, or project parameters, we execute comprehensive Non-Disclosure Agreements (NDAs). All analytical datasets, formulation recipes, synthesis pathways, and patents generated during a project remain the exclusive, 100% intellectual property of our client.

Our laboratory operates under strict GLP (Good Laboratory Practice) and GMP-aligned quality frameworks. We follow European Pharmacopoeia (Ph. Eur.) and International Council for Harmonisation (ICH) monographs. Every assay, stability run, and purity test is performed using calibrated instrumentation with complete audit trails and verified data integrity.

Yes. With our registered foundation in patenting pharmaceutical preparations (patentiranje farmacevtskih izdelkov), we assist pharmaceutical manufacturers, biotech innovators, and research institutions in formulating stable dosage forms and preparing robust experimental documentation to substantiate patent claims and regulatory filings.

We offer complete stability programs following ICH Q1A–Q1F guidelines, including accelerated stability (40°C ± 2°C / 75% RH ± 5% RH), intermediate stability (30°C ± 2°C / 65% RH), long-term stability (25°C ± 2°C / 60% RH), and photostability testing. We also execute forced degradation profiling to elucidate breakdown mechanisms under acid, base, oxidation, and thermal stress.

Our facility houses state-of-the-art analytical equipment including High-Performance Liquid Chromatography (HPLC) with UV-Vis and Photodiode Array (PDA) detectors, Gas Chromatography-Mass Spectrometry (GC-MS), dissolution testing baths, spectrophotometers, Karl Fischer titrators, precision pH/conductometers, and climate-controlled stability chambers.

Initiating a study is straightforward: contact our team directly at research@kvlab.si or submit an inquiry using our online form. Our scientific team will schedule an introductory technical discussion under an NDA, assess your project parameters, and deliver a tailored study proposal with clear milestones, timelines, and deliverables.

Upon study completion, partners receive a comprehensive Certificate of Analysis (CoA), full raw chromatograms and spectral data, validated method transfer protocols, and an extensive formal technical report formatted to facilitate straightforward regulatory review by the European Medicines Agency (EMA) and national health authorities.