Aligned. Compliant. Delivered.
Coherence Scientific
Coherence Scientific bridges the world's most demanding regulatory environments "Connecting Quality compliant, WHO-GMP certified manufacturing in India with buyers across the Globe. Every shipment we deliver is compliant before it leaves the facility.
"Coherence Scientific: Ensuring Supply Chain Resilience."
Coherence Scientific is a pharmaceutical company with regulatory intelligence. In an era of increasing global drug shortages and geopolitical supply chain fragmentation, we serve as the strategic bridge between high-capacity, WHO-GMP certified manufacturing in India and critical healthcare requirements in the USA, EU, and MENA regions.
By leveraging real-time data from authentic sources, we identify regulatory vulnerabilities and secure supply lines for pharmaceuticals. Our focus is on statutory reliability, thereby ensuring life-saving and critical care medicines reach their destination without the delays associated with compliance.
We supply APIs and Finished Dosage Formulations across the USA, Europe, the Middle East, Latin America, and Southeast Asia.
Our operations are built on a single principle: every product we put our name on must meet the full regulatory standard of the destination market, with documentation that is complete, traceable, and audit-ready before the first shipment leaves the warehouse.
Every product we supply comes with the complete documentation required by country-specific regulatory authorities. Explore our full product portfolio on the Home page →
Our buyers operate in the world's most demanding regulatory environments such as the USA, EU, MENA, Latin America, Southeast Asia, and many more. We at "Coherence Scientific" are capable & equipped to deliver the needs. See our full regulatory reach →
The People Behind Every Commitment
Our Team
Our leadership team has personally commissioned cGMP pharmaceutical facilities, prepared and filed CTD/eCTD dossiers for the USA, EU, and MENA markets, and built direct supply relationships with hospital procurement agencies and ANDA holders. Every commitment we make to a buyer is grounded in experience our team has already delivered.
What We Bring
Our Expertise
Pharmaceutical Manufacturing & GMP
Our leadership has operated and commissioned cGMP pharmaceutical facilities, from equipment qualification (IQ/OQ/PQ) through batch documentation, quality release, and GMP inspection readiness. We understand what it takes to produce and export a GMP-compliant product.
Regulatory Affairs: USA, EU, MENA
Our regulatory team has prepared and submitted CTD dossiers, Type II DMFs, EDQM CEP applications, and WHO Prequalification dossiers. We maintain active relationships with regulatory consultants in each target market.
Quality Systems & Documentation
We maintain a Quality Management System (QMS) governing all supply engagements: supplier qualification standards, quality agreements, batch record governance, and deviation management. Every manufacturing partner operates under our quality oversight.
Business Development & Market Access
Our business development team is engaged in regular conversation with key decision makers across target geographies to understand and fullfill the requirements efficiently.
The Case for Coherence
Why Partner With Coherence Scientific
Complete documentation as standard
Every product is supplied with comprehensive documentation and market-specific registrations.
Multi-market regulatory filing capability
We file and maintain regulatory documentation in various territories based on our customer requirement.
Pre-qualified manufacturing network
Every manufacturer in our supply network is audited against our qualification standards before the first commercial engagement. Audit reports, quality agreements, and GMP certificates are on file and available to buyers.
Supply continuity by design
With pre-mapped alternate raw-material sources and proactive logistics planning built in we ensure that a capacity or quality event at any single facility never interrupts your supply chain.
Traceability
Every shipment destined for every market is compliant with serialization and end-to-end batch genealogy as a standard component of delivery.
Regulatory intelligence and proactive sourcing
Our portfolio is assembled through systematic data analysis. We identify supply opportunities before the market does.