Active Pharmaceutical Ingredients · Finished Dosage Formulations · Global Regulatory Compliance
"Proven Molecules. Precise Compliance"
Coherence Scientific is a Hyderabad-based pharmaceutical supply company delivering Active Pharmaceutical Ingredients and Finished Dosage Formulations to Global Clientele. Every product we supply is backed by complete regulatory documentation such as DMFs, CTD dossiers, COPPs, GMP certificates, and market-specific registrations in the exact format required by the destination regulatory authority.
Who We Are
Purpose
Ensuring critical medicines are available, compliant, and reliably delivered "Every time".
Mission
To create shared, long-term value for our buyers, our manufacturing partners, and our investors, by ensuring reliable access to essential and niche medicines through rigorous quality systems, regulatory stewardship, and a compliance-led supply network that we build and govern ourselves.
Vision
To be the most trusted partner in pharmaceutical supply chain via advancing resilient access to niche and critical therapies while delivering transparent, compliant, and sustainable outcomes for every stakeholder we serve.
What Guides Us
We select and prioritize molecules using evidence, clinical need, and feasibility.
Compliance is not a checkpoint; it is embedded in qualification, documentation, and every release decision.
We maintain end-to-end traceability and provide complete, consistent documentation that stands up to scrutiny.
When we commit under a quality agreement, we own outcomes and resolve issues decisively.
We respond quickly to demand shifts and shortages by aligning capable manufacturing with clear regulatory pathways.
We measure success by sustained trust, continuity of supply, and long-term collaboration with buyers and manufacturers.
Our Portfolio
"Where compliance meets chemistry."
Supply high-purity bulk drug substances from USFDA, EU-GMP, and WHO-GMP certified manufacturing facilities.
"The intelligence behind every dose."
Tablets, Capsules, Ophthalmic, Topical formulations and Sterile injectables.
"Mastering the science of global compliance."
Each product supply includes the comprehensive regulatory package based on customer's regulatory needs inline to the approved dossier format required by the importing authority.
Clinical Focus
Our product portfolio spans major therapeutic categories, selected for clinical significance, global demand, and long-term supply reliability.
Global Presence
Our products enter every market with documentation that fully meets the standard of each regulatory authority. COMPLETE. TRACEABLE. AUDIT-READY.
Filing
Type II DMF, eCTD
Channel
503B outsourcers, ANDA holders
Standard
USFDA cGMP · DSCSA
Filing
CTD dossier, CEP (EDQM)
Procedure
DCP / MRP
Standard
EU-GMP · EU FMD
Authorities
SFDA, MOHAP, EDA, KIMADIA
Format
CTD + COPP
Track
WHO Essential Medicines
LatAm
ANVISA, COFEPRIS, INVIMA
SEA
BPOM, FDA PH, MOH VN
Format
CTD / ACTD
Get Started
Receive product availability, regulatory status, pricing, and your complete documentation package within a business day.
Submit an enquiry →Gain access to established regulatory market channels across the USA, EU, MENA, and Southeast Asia. We review and respond within five business days.
Register your facility →Build your career at the intersection of pharmaceutical science, global compliance, and supply chain innovation. We welcome strong profiles at any time.
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