Our quality control (QC) testing of pharmaceuticals is very rigorous and involves multiple techniques including elemental analysis techniques. Quality controls include verification of identity, purity and potency.

For Research & Development, we use a diverse range of methods to investigate the chemical nature of substances with the aim to identify, quantify and understand the substance and how it behaves in different conditions.

The objective of cleaning validation is to prove that the equipment is consistently cleaned of product, detergent and microbial residues to an acceptable level, to prevent possible contamination and cross-contamination of pharmaceutical starting materials and products.

The purpose of identification testing is to verify the identity of the active pharmaceutical ingredient (API) on the pharmaceutical tablet. The identification test will be able to discriminate between compounds of nearly related structures that are probably present.

Modernizing the old art of herbal medicine practice requires addressing the three interrelated issues of Quality, Safety, and Efficacy. The pharmaceutical quality of plant medicines is critically important as it does also affect the efficacy and safety of the drugs.

It enables you to immediately streamline your microbial contamination testing workflow and leverage your quality assurance level by avoiding the risk of exogenous contamination.

Elemental analysis instruments deliver quality, reproducible data from any sample type. It analyzes samples to meet even the strictest regulations and legislation. So you can have total confidence in your results.

Products such as multi-dose pharmaceutical medicines, cosmetic products, personal care products will normally contain preservatives and needs to be tested. Therefore, Preservative efficacy testing (PET) or antimicrobial effectiveness testing (AET) is required for the assessment of the antimicrobial preservation of multiple-use cosmetic and pharmaceutical products.

Toxic and nontoxic contaminants can negatively affect the performance of materials, products, paints and coatings. We offer contamination testing to help you characterize impurities, determine their source and prevent them from reoccurring.

Method Validation is used to confirm that the analytical procedure employed for a specific test is suitable for its intended use and is required for complete compliance with international regulatory guidelines.

Our services are aimed at ensuring the quality and purity of raw materials used in the production of biologicals for the pharmaceutical and biotech industries.

Organic volatile impurities are residual solvents that are used in and are produced during the synthesis of drug substances, or in the production of drug formulations. Many of these residual solvents generally cannot be completely removed by standard manufacturing processes or techniques.

Every lot of product produced requires a series of tests to ensure active ingredients are free of contaminants. All products being released into the global pharmaceutical markets require testing of final product packages to demonstrate compliance with regulatory guidelines. We offer

The purpose of stability testing is to provide evidence on how the quality of a drug substance or drug product varies with time under the influence of a varietv of environmental factors such as temperature, humidity, and light, and to establish a re-test period for the drug substance or a shelf life for the drug product and recommended storage conditions.

This toxicity test use specific aquatic and terrestrial microorganisms to mesure biological response to specific contaminants or mixes of contaminants. It also mesures the light output of luminescent microorganisms that emit light as a normal consequence of respiration.

The nutrition facts label (also known as the nutrition information panel, and other slight variations) is a label required on most packaged food in many countries, showing what nutrients are in the food. our analytical testing can help you to meet regulatory requirements and protect your brand

It is necessary to understand the total each content in a sample or in a formulated product. Accurate quantification is important, as a range of other critical assays require precise total content results in order to generate data.

Total Organic Carbon (TOC) is a mesure of the total amount of carbon in organic compounds in pure water and aqueous systems. TOC is a valued, analytical technique that is applied to determine how suitable a solution is for their processes. Unless it's ultrapure, water will naturally contain some organic compounds, understanding how much is key.

Analyzing pesticide residues on commodities of vegetal origin which are used in the composition of medication, is part of the protection of public health. Each essential oil or plant extract has special features which can have an influence on the analysis results.

Our chemical industry consultants bring comprehensive talent development capabilities to Chemical and Process Industries.

Chemical contaminants are substances that have been nintentionally added to food. Some chemical contaminants are formed naturally, while others come from environmental contamination.

-Full microbiology panel for NPN and DIN products as per USP 60/61 and USP 2021/2022 and all other pharmacopeias -Microbiology Analytical Testing -Microbial Limits Tests and Bioburden -Sterility Testing -Bacterial Endotoxins Testing -Water Testing and Environmental Monitoring -Microbial Contaminant Identification -Antibiotic Assays -Antimicrobial Effectiveness Test -Particulate Matter

Fast, accurate and high quality SPF and sunscreen testing.