Our Experience

RxCloud is a professional services organization focused exclusively on Pharma, Biotech and Medical device industries. We are a full-scale Quality Assurance Organization driving innovation & ensuring compliance across the industry. Our mission is to deliver Quality, Compliance, Innovation, Customer Experience, and speed that enables global Life Science industry to continuously innovate and significantly reduce drug development life cycle.
We are specialized in providing the CSV services, GxP Audits (GMP, GDP, GLP, GCP, GVP) as a service, Veeva Services, Software Quality Assurance services. Our full spectrum of service offerings includes QMS Consulting, End to End Global Audit Management, CAPA management, SOP Authoring, QA as a service. RxCloud’s differentiation is bringing in speed and agility to achieve compliance first time and every time.

Ask Us About

  • QA as a Service
  • GxP (GMP, GLP, GCP, GVP) audits
  • CSV / CSA Consulting
  • QMS development / SOP authoring
  • CAPA management
  • GxP Validation of Life Sciences products / devices
  • Test Automation & Performance Engineering
  • Veeva Clinical, Regulatory, Safety & QMS


Our Approach

RxCloud believes in innovation and enhanced customer experience. Our approach includes a thorough process consultation to help identify gaps and opportunities in the areas of Life Sciences and recommend innovative solutions across the various business processes. RxCloud also offers a suite of accelerators and frameworks to aim IT to reach the business goals faster and easier.



    RxAMS – Audit Management System

    End to End validated Audit management system designed to manage GxP audits (Internal & external) for global organizations. System powered by Optimized audit scheduling and execution with transparent insights.



    Pre-written automated solutions refer to software tools or programs that are designed to perform a specific task or set of tasks automatically. These solutions can help save time and reduce the risk of errors during the data migration process.



    A multiple data migration tool allows for the transfer of large volumes of data between different systems or platforms, providing a more efficient and streamlined approach to data migration.



    A continuous compliance framework is a set of processes and procedures that ensure regulatory compliance on an ongoing basis. It involves the use of automated tools and monitoring techniques to maintain compliance with changing regulations.


Why Choose Us

We bring Speed & Agility to Life Sciences industry with focus on compliance and first time right. Talk to us to know more.