At Coral Drugs, we believe that innovation, precision, and commitment to quality are the foundation of pharmaceutical excellence. With decades of experience and a strong global presence, we have established ourselves as a trusted partner for Active Pharmaceutical Ingredients (APIs), intermediates, and custom synthesis. Our goal is to deliver reliable, high-quality products and services that meet the most demanding global standards.

Core Competency & Expertise

Our strength lies in our team of over 200 highly skilled professionals, including chemists and process experts, who are dedicated to ensuring superior quality in every step of production. We foster a culture of innovation, where ideas evolve into solutions that enhance process efficiency, reduce turnaround times, and maintain cost-effectiveness. Every member of our team is driven by a shared mission: to contribute to the development of safe, effective, and accessible pharmaceutical products worldwide.

Integrated Operations

Coral Drugs operates with a fully integrated approach to API development and manufacturing. From laboratory-scale reactions to kilogram and multi-ton productions, our facilities are equipped to manage every aspect of process design and execution. Our analytical support systems include advanced chromatographic and headspace analysis for volatile impurities, ensuring accuracy and consistency across all batches. This seamless integration allows us to maintain agility, flexibility, and reliability in meeting diverse client requirements.

Development-to-Launch Partner

Our capabilities extend far beyond manufacturing. We serve as a complete development-to-launch partner, guiding clients through the entire product lifecycle from early research and process optimization to pilot plant production and cGMP scale-up. Leveraging our extensive cGMP expertise, we also provide comprehensive support for global regulatory filings. This end-to-end approach ensures that our clients experience a smooth, efficient, and compliant path from concept to commercialization.

Global cGMP Compliance

Quality and compliance are the cornerstones of our operations. Coral Drugs’ facilities are approved by multiple international regulatory bodies, including the FDA and EU authorities. We adhere to stringent global quality standards and routinely undergo audits from major regulatory agencies across the USA, EU, Mexico, Korea, Japan, and India. Our compliance-driven framework ensures that every product we deliver meets the highest levels of safety, consistency, and performance.

Client-Centric Approach

At Coral Drugs, our clients are at the heart of everything we do. We adopt a client-centric approach, with dedicated account management to deliver personalized support, transparent communication, and collaborative partnerships. We believe in building long-term relationships founded on trust, integrity, and mutual success.

Our Strengths at a Glance

• Global, approved regulatory filings
• Expertise in particle sizing
• Strong focus on respiratory segments and high-potent APIs
• Vertically integrated intermediate manufacturing
• Multi-purpose production blocks for niche and custom products

From development to delivery, Coral Drugs combines scientific excellence with operational precision to bring value and reliability to every partnership. Our vision is to continue leading with innovation, enabling better healthcare outcomes through superior pharmaceutical solutions.

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