Founded in 1984 with headquarters in Hyderabad, India, VIMTA LABS LTD., is a leading contract research and testing organization, providing bio/pharmaceutical companies an integrated scientific, technical and regulatory expertise to support all stages of drug development and manufacturing process. Our service portfolio includes preclinical and clinical research; and cGMP laboratory services viz., method development & validations, microbiology, stability testing, extractables & leachables, process validation, quality control, physical characterization etc.
In our 34 years of journey, we have gained in-depth scientific and technical expertise through working with a variety of molecules and formulations in different therapeutic areas. We support the needs of more than 300 bio/pharmaceutical companies across the globe, from virtual to large pharma and biopharma through a wide range of expertise. Our team of 1100+ professionals constantly endeavor to provide timely scientific solutions and services to help customers manage their drug development and manufacturing processes more efficiently, without compromising on quality.
We have a track record of strict compliance to regulatory requirements (cGMP, GLP, GCP) and Standards (ISO 17025, ISO 15189, ISO 9001), and have undergone over 70 regulatory audits successfully from regulatory agencies across the globe including USFDA, WHO, MHRA, Afsaaps, BfArM, DCGI, NGCMA, and DRAs of Denmark, Sweden and Portugal. This has earned us the trust of our customers!