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Pharmaceutical Testing
- Nitrosamine testing lab services are in demand ever since the prescription pharmaceutical drug ranitidine and subsequently may rugs like metformin, sartans etc have been in the news for nitrosamine contamination.
- Inorganic Impurities are a critical quality attribute of drug substance and drug products because they have the potential to affect the safety and efficacy of the product. The regulatory and compendial standards for the control of impurities continue to evolve due to advancement in analytical science, technology and toxicology.
- Method validation is defined as the generation of documented evidence which establishes the suitability of the method for its intended use. As part of the method validation, a number of parameters are required to be established and must meet the global acceptance criteria laid down under the ICH guidelines and in the various pharmacopoeia.
- Stability testing is integral to developing new pharmaceutical products and active pharmaceutical ingredients, to establish their shelf life or expiry date. It is also equally important along with ongoing routine manufacturing to monitor product quality as a function of time. We provide a complete solution to your requirements of Stability Studies for Shelf-Life Estimation.
- Raw material testing is crucial for ensuring safety, quality and efficacy of pharmaceutical products. There are many things to be considered that could impact the way raw materials need to be blended, such as polymorphism, the particle size of raw materials and other properties.
- Microbiological testing plays an important role in the production of pharmaceutical drug substances and drug products.
