About Us
What is 'JivRx'
Jiv ( जिव ) — A Sanskrit word, meaning life or soul.
Rx — The symbol for medical prescriptions.
It reflects our mission to empower pharmaceutical companies with life-centered, strategic, and regulatory guidance.
At JivRx,
We are a specialized pharmaceutical consulting firm offering end-to-end solutions across Recruitment, Regulatory Consulting, and Pharmaceutical Trade. With a strong foundation in industry expertise and compliance, we support clients across the pharmaceutical, healthcare, and life sciences sectors. Whether you're scaling your team, setting up a new plant, or sourcing critical APIs, we bring strategic guidance, operational excellence, and global networks to every project.
Our Vision and Mission
Our Vision
To become a world-class consulting firm that bridges the compliance gap between regulators and organizations — driving global standards, operational excellence, and regulatory readiness.
Our Mission
Our mission is to empower SMEs and emerging enterprises by delivering fact-based solutions, ethical guidance, and practical implementation strategies — fostering sustainable compliance and business integrity.
We recognize that small and growing businesses often face unique challenges in understanding and meeting evolving regulatory requirements. At the same time, they operate with limited resources, making it critical to provide support that is not only accurate and compliant, but also realistic and scalable. Through our hands-on consulting approach, we ensure that every recommendation is grounded in regulatory reality, tailored to client needs, and implementable within their operational framework.
Beyond compliance, we believe in building a culture of integrity, quality, and accountability. Our goal is not just to help clients pass audits or meet checklists — but to embed long-term systems that enhance efficiency, minimize risk, and promote trust across stakeholders, regulators, and global partners. We strive to be a reliable growth partner, guiding businesses from foundational compliance to global regulatory readiness.
Our Team
Experienced. Multidisciplinary. Global.
Our team comprises seasoned professionals with hands-on expertise in pharmaceutical and biotechnology dosage forms, including solid, semi-solid, and liquid formulations — across both sterile and non-sterile platforms. From early development to commercial manufacturing, our experts bring in-depth understanding and practical experience across diverse product categories and regulatory landscapes.
We are proud to bring together:
Quality Experts – Specializing in cost-effective quality solutions, data integrity compliance, and remediation strategies aligned with global standards continuous improvement across sterile and non-sterile operations.
Operational Experts – Driving efficiency in manufacturing, technology transfer, and batch execution with deep process knowledge.
Engineering Experts – Designing, qualifying, and maintaining GMP-compliant equipment and facilities that support various dosage forms.
Regulatory Affairs Experts – Guiding global product registration, dossier preparation (CTD/eCTD), and audit readiness.
IT and Security Experts – Supporting data integrity, electronic systems validation (CSV), and pharma-grade cybersecurity.
Project Management Experts – Leading end-to-end execution of strategic initiatives with cross-functional coordination.
Analytical Experts (QC & Microbiology) – Delivering accurate and compliant testing for raw materials, finished products, and environmental controls.
Business Development and Marketing Experts – Strategically expanding market presence, identifying growth opportunities, and building strong client relationships.
With a multidisciplinary approach and deep domain knowledge, our team enables clients to navigate complex challenges, achieve regulatory compliance, and drive innovation in the life sciences sector.