Pharmaceutical products analysis is a vital aspect of ensuring the safety and efficacy of medicinal products. The process involves meticulous testing and evaluation to ensure that the finished products meet the required standards. One crucial component in this process is the testing of raw materials, which is essential in guaranteeing the quality and integrity of the final product. Compliance with organic impurities, elemental impurities, and residual solvents is of utmost importance to ensure the safety and efficacy of pharmaceutical products. Additionally, in vitro bioequivalence analysis, assay, and related substances play a critical role in the approval of pharmaceutical products. USFDA, NABL, CDSCO approved Pharmaceutical products testing labs play a pivotal role in carrying out all these necessary analyses and evaluations to ensure the highest level of quality and safety in pharmaceutical products. With their expertise and state-of-the-art facilities, these pharmaceutical testing laboratories contribute significantly to the overall integrity and reliability of the pharmaceutical industry. These labs also conduct sterility testing to ensure that the pharmaceutical products are free from any harmful microorganisms. Their work is instrumental in preventing any potential risks and ensuring that only safe and effective medications reach the market. As the pharmaceutical industry continues to evolve and grow, the role of pharmaceutical testing labs become increasingly important in ensuring the highest standards of quality and safety in medicinal products.

So, when it comes to pharmaceutical products testing, relying on reputable and accredited labs is essential for both regulatory compliance and consumer confidence. The Solution Analytics offers support in collaborating with USFDA, CDSCO & NABL accredited Medicine Testing Laboratories to conduct USP, AOAC, EP/BP, Non-Pharmacopeial tests in various product categories, including API, excipients, and finished products like tablets, capsules, oral liquids, injectables, oral suspensions, gels, and transdermal patches. A range of tests, including API analysis, excipient analysis, microbiological testing (BET & MLT), extractable and leachable, glass delamination studies, dissolution testing, bio-waiver testing, and residual solvent, would be provided. Sterility Testing of Pharmaceutical Products is also given special attention. If you are facing any challenge in conducting HPLC,/UPLC (UV/PDA/ELSD/IR detectors) analysis, LCMS/GCMS testing, AAS testing, Malvern Particle Size detector, Viscometer, Rheometer, USP Type III & Type IV dissolution apparatus etc., you are just a step away to reach experienced service providers for all your analytical needs. Fill the request for quotation form, register yourself & let the system work for you to get requisite services.

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