Healing Lives. Advancing Science.Defining Tomorrow.®
We are Aurexa, a pharmaceutical company rooted in the belief that access to quality medicine is a fundamental human right. Established in 1985, we have grown from a single manufacturing unit in Gujarat to a globally recognized pharmaceutical organization with a presence in 24+ countries.
Our Elite ProductPortfolio
Explore our comprehensive range of pharmaceutical products — each one crafted with precision, global compliance, and unwavering quality standards.
Pharmaceutical Sector
01
Formulation Development
Active Pharmaceutical Ingredient (API) synthesis with strict adherence to ICH Q7 guidelines. Our dedicated API manufacturing block delivers high-purity bulk drug substances for both domestic and international markets. Fully WHO-GMP and CDSCO compliant with real-time quality monitoring.
02
Contract Manufacturing (CMO/CDMO)
End-to-end contract manufacturing for domestic and global pharmaceutical brands. From process development to large-scale production, our GMP-certified infrastructure enables fast, cost-efficient, and quality-assured manufacturing for your molecules.
03
Drugs Manufacturing
Active Pharmaceutical Ingredient (API) synthesis with strict adherence to ICH Q7 guidelines. Our dedicated API manufacturing block delivers high-purity bulk drug substances for both domestic and international markets. Fully WHO-GMP and CDSCO compliant with real-time quality monitoring
World-classQuality
Years of Excellence
25+
We offers exciting job opportunities and careers around the globe. Come be a part of our PROUD (Passion, Resilience, Ownership, TrUst & Decisiveness) culture and embrace the challenges and new opportunities as we work together to enable our clients and benefit patients worldwide.
Products Manufactured
1108+
Countries Served
26+
Therapeutic Categories
60+
Indian Pharma Market Size
₹50B+
Our Expertise

Research and development
Innovation Before Industry
We transform scientific curiosity into life-saving medicines through rigorous discovery, data-driven insights, and a relentless commitment to human health.

Policies & Practices
Compliance Without Compromise
Our quality management system is built on ICH guidelines, WHO-GMP standards, and a zero-tolerance culture toward deviation without documented justification.

Technology Integration
Digitally Driven Science
We deploy Manufacturing Execution Systems that digitize every step of production, eliminating paper-based errors and delivering complete electronic batch records with full audit trails.

Got Questions?We Have Answers.
That’s why we focus on high-impact innovation that adapts to your life, providing the daily motivation and technical expertise needed to elevate your business journey.
Our facility is WHO-GMP Certified, ISO 9001:2015 compliant, and aligned with USFDA and EU-GMP manufacturing standards. We are also registered with CDSCO and comply with Schedule M of the Drugs & Cosmetics Act, India.
Yes. Our facility follows USFDA current Good Manufacturing Practices (cGMP) guidelines and is EU-GMP aligned. We have successfully exported to over 50 countries including regulated markets in North America and Europe.
Typical formulation development takes 4–8 months depending on the complexity of the molecule. Our QbD-driven process and experienced R&D team help reduce development timelines significantly
We manufacture and deliver safe, effective, and affordable medicines that improve the quality of life for patients worldwide — without compromise.
● Our Method
We deliver industry excellence and customer satisfaction
Our pharmacovigilance team monitors product safety post-launch, manages adverse event reporting, and ensures ongoing compliance with regulatory post-approval commitments.
A Structured, Transparent, and Collaborative Journey.
Join a Team of 200+ Scientists, Innovators & Change-Makers.

Our Quality Infrastructure:
• In-house NABL-accredited analytical testing laboratory• Real-time environmental monitoring systems in manufacturing zones• 21 CFR Part 11-compliant electronic batch records• Validated cleaning procedures with dedicated QC team• Annual third-party quality audits and regulatory inspections• Dedicated Pharmacovigilance and Drug Safety team
Sub-Services Under Quality
Whether you are at a hotel gym or in your living room, your coach builds a dynamic schedule that fits your available equipment and energy levels so you never have to guess what exercise comes next to see real progress.
Green Sustainable Practices
We emphasize the need for decarbonization and collectively work towards the goal of net-zero emissions. Substantial installation of renewable energy power plants helps us progress towards our target of meeting net-zero energy requirements by 2027. We are also proud signatories to the India Global Compact, pledging to actively contribute to the creation of a sustainable future.
Let's Build Something That Matters.
Reach out today — your next pharmaceutical partnership begins with one conversation.
Tel: +44 (0)20 7405 7686
info@youremail.com













