We build LIMS software that labs trust for compliance, traceability and efficiency — deployed across hundreds of sites in India and beyond.
To provide prompt, consistent, reliable and cost-effective quality services to various sectors worldwide, maintaining confidentiality and integrity.
Oasis is a diversified organisation with a strong presence in the Indian pharmaceutical and quality ecosystem, with over three decades of industry experience. The group operates across pharmaceutical manufacturing, contract analytical and research services, and specialised software solutions for quality and laboratory management.
The group’s corporate and business development centre, serving the pharmaceutical industry for over two decades through innovative, high-end software solutions — with diverse assignments delivered across India and international markets.
Operates modern GMP / ISO-certified manufacturing facilities focused on the development and manufacture of high-quality therapeutic formulations, backed by strong quality systems and ethical business practices — including contract manufacturing for several reputed pharmaceutical companies.
Operates ISO-certified, NABL-accredited and government-approved testing laboratories equipped with sophisticated analytical instrumentation — providing reliable analytical testing and quality evaluation services, and a preferred quality-testing partner built on technical excellence and customer service.
Oasis brings together pharmaceutical manufacturing expertise, analytical and research capabilities, and advanced laboratory software technology — enabling integrated solutions across the pharmaceutical and allied industries.
Three decades of industry experience, two decades of software innovation, and one integrated commitment to Quality, Compliance & Excellence.
Validated on GAMP guidelines and compliant with every major international regulation governing laboratory data integrity.
Full electronic records, e-signatures and audit trails — ready for FDA inspection.
Method traceability and results aligned to the global testing & calibration standard.
Data integrity, good lab and manufacturing practices across the entire sample lifecycle.
Compliant with UK MHRA guidelines for pharma quality and data governance.
Watch how OasisLIMS streamlines laboratory workflows, R&D, stability studies and data-integrity compliance — straight from our channel.
Visit our channel →Everything we hand to a lab that is evaluating us — the full product portfolio, our QC activities booklet, and a plain-language guide to Schedule M. Free to download, no form to fill in.
