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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.
We can support clients with sampling protocols and analysis of swab samples from cleaning validation and samples of final products to establish the absence of the Beta-Lactam products earlier manufactured in the facility
Related substances test is required to control degradation impurities. Its objective is to limit the impurities which occurs during synthesis of active pharmaceutical ingredient.
We provide a complete solution to support water system validation including, microbiological testing, chemical testing , endotoxin testing, Volatile Organic Compound(VOC) , sample transportation and sample collection.
Process validation is essential in pharmaceutical, API and medical device . It is important in concept development, quality risk management and quality systems at all stages of manufacturing process lifecycle.
We offer a complete package of pharmaceutical testing services for finished products for both the domestic as well as export markets.
The pharmaceutical products that are not true solutions require dissolution testing as the dissolution rate affects the bioavailability
Particle size analysis lab is routinely required by industries as a critical control parameter for raw materials, manufacturing processes, and finished products.
Microbiological testing plays an important role in the production of pharmaceutical drug substances and drug products.
Excipients are pharmacologically inactive materials from different origins (biological or biotech products, minerals, chemical synthesis-based, etc.)
We provide comprehensive range of solid state services in compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) programs.
After the drug has been formulated, the reports from the clinical trials are forwarded to be approved by the regulatory body for pharmaceuticals and medical devices – FDA in the US and The Central Drugs Standard Control Organization (CDSCO) in India.
Auriga Research has a state of the art laboratory with equipment and analytical methodologies like: Chromatography (TLC, GC, HPLC, HPTLC, GC/MS, LC/MS/MS, GPC, Headspace Analyzer); Spectroscopy (FTIR, UV/visible, Atomic Absorption) Spectrometry (ICP/MS);
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Arbro Analytical Division 4/9 Kirti Nagar Industrial Area New Delhi - 110015 India
Auriga Research Pvt. Ltd.
Dev Chaudhry Complex Baddi Nalagarh Road, District Solan, Himachal Pardesh 174102
India
Auriga Research Pvt. Ltd.
Plot No. 136, Sector 5, IMT,
Manesar-122052
Haryana
India
Auriga Research Pvt. Ltd.
No. 136, 6th cross, 2nd stage
Yeshwanthpur Industrial Suburb
Bangalore - 560022, Karnataka
India
Arbro Analytical Division 4/9 Kirti Nagar Industrial Area New Delhi - 110015 India
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