NOVA LABS CO provides independent laboratory testing for research peptides, chemical compounds, raw materials, and finished formulations. Our work is focused on clear analytical data, traceable reporting, and certificate verification that helps clients make informed quality decisions.
From peptide purity and identity confirmation to impurity profiling, residual solvent screening, heavy metal analysis, endotoxin testing, and full certificate of analysis documentation, our laboratory process is designed to bring structure, transparency, and scientific confidence to every submitted sample.
Questions? Email contact@novalabsco.com
Send your sample information, select the required testing service, and begin the laboratory submission process.
Submit SampleConfirm the authenticity of a Certificate of Analysis using the verification page.
Verify COAModern peptide and chemical testing requires more than a simple pass or fail result. A useful report should explain what was tested, how it was tested, what the analytical data shows, and whether the sample matches its expected identity and composition. NOVA LABS CO focuses on producing results that are readable, defensible, and useful for decision-making.
Many samples submitted for testing may contain synthesis-related impurities, incomplete sequences, degradation products, salt forms, moisture, residual solvents, or trace contaminants. Our role is to evaluate these factors using appropriate analytical methods and then present the findings in a clear report supported by instrument data.
Our process is designed to keep sample submission organized, confidential, and easy to follow.
Place your request, label your sample properly, and send it to the laboratory with the required submission information. Once received, the sample is logged and prepared for analysis.
Depending on the testing package, our team may evaluate purity, molecular identity, content, solvents, metals, endotoxins, or other quality markers using validated laboratory methods.
Results are delivered in a structured report that may include chromatograms, spectra, method references, calculated values, observations, and certificate verification details.
Use the submission page to begin the process and provide the required sample details.
Go to Submit PageVerify whether a COA belongs to NOVA LABS CO and confirm its report information.
Check COAIndependent testing gives researchers, manufacturers, distributors, and quality teams an objective view of sample quality. Instead of relying only on supplier claims, clients can review analytical evidence that confirms whether a material appears to match its expected identity, purity, and composition.
This is especially important for peptides and specialty compounds, where small changes in sequence, degradation, moisture content, incomplete synthesis, or contamination can affect the reliability of downstream research or formulation decisions.
About Our LaboratoryOur laboratory supports a range of analytical testing needs for peptide, chemical, and formulation quality review.
HPLC and UHPLC methods are used to separate the main compound from related impurities, degradation products, and minor peaks that may appear in the sample profile.
Mass spectrometry can help confirm whether the observed molecular weight matches the expected compound, sequence, or target material.
Quantitative testing estimates the amount of target material present and may account for salts, water, counter-ions, or other factors that affect actual content.
Impurity review may identify truncated sequences, deletion products, dimers, aggregates, synthesis byproducts, or degradation-related compounds.
Amino acid composition testing can support peptide content confirmation by measuring residue composition after hydrolysis.
Microbiological safety testing can screen for endotoxin burden and viable microbial contamination depending on sample type and client requirements.
Trace metals testing helps detect elemental contaminants that may originate from raw materials, synthesis, processing equipment, or packaging.
GC-based solvent screening helps identify volatile residues that may remain from synthesis, extraction, purification, or formulation processes.
Used when the main question is whether the sample is clean, whether additional peaks are present, and how the target material compares against the total chromatographic profile.
Used when the key concern is whether the molecular mass or identity corresponds to the expected peptide, compound, or submitted reference information.
Reports can be structured to include sample details, testing method, result summary, analytical observations, and supporting instrument data.
Start a new laboratory request and provide the details needed for sample intake and analysis.
Submit New SampleUse the verification tool to confirm report authenticity and review certificate information.
Validate CertificateWhether you need a single purity report or a broader analytical package, our team can help organize the right testing approach for your sample type.