Active Pharmaceutical Ingredients · Finished Dosage Formulations · Global Regulatory Compliance

Globally Compliant APIs and
Finished Dose Formulations

"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, Mission & Vision

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

Values

01

Science-led portfolio choices

We select and prioritize molecules using evidence, clinical need, and feasibility.

02

Regulatory rigor, built-in

Compliance is not a checkpoint; it is embedded in qualification, documentation, and every release decision.

03

Audit-ready transparency

We maintain end-to-end traceability and provide complete, consistent documentation that stands up to scrutiny.

04

Accountability without ambiguity

When we commit under a quality agreement, we own outcomes and resolve issues decisively.

05

Operational agility

We respond quickly to demand shifts and shortages by aligning capable manufacturing with clear regulatory pathways.

06

Partnership over transactions

We measure success by sustained trust, continuity of supply, and long-term collaboration with buyers and manufacturers.

Our Portfolio

What We Supply

Active Pharmaceutical Ingredients

Active Pharmaceutical Ingredients (APIs)

"Where compliance meets chemistry."

Supply high-purity bulk drug substances from USFDA, EU-GMP, and WHO-GMP certified manufacturing facilities.

Finished Dosage Formulations

Finished Dosage Formulations (FDFs)

"The intelligence behind every dose."

Tablets, Capsules, Ophthalmic, Topical formulations and Sterile injectables.

Regulatory Compliance Documents

Regulatory Compliance Documents

"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

Therapeutic Areas

Our product portfolio spans major therapeutic categories, selected for clinical significance, global demand, and long-term supply reliability.

Oncology Anti Diabetic / Metabolic Disorders Anti Psychotics Anti-Infectives Cardiovascular Health Critical Care & Specialised Medicine Hormones & Reproductive Health Ophthalmology Urology & Men's Health

Global Presence

Our Regulatory Reach

Our products enter every market with documentation that fully meets the standard of each regulatory authority. COMPLETE. TRACEABLE. AUDIT-READY.

Global regulatory reach map

USA · FDA

Filing

Type II DMF, eCTD

Channel

503B outsourcers, ANDA holders

Standard

USFDA cGMP · DSCSA

Europe · EMA

Filing

CTD dossier, CEP (EDQM)

Procedure

DCP / MRP

Standard

EU-GMP · EU FMD

MENA · SFDA / MOHAP

Authorities

SFDA, MOHAP, EDA, KIMADIA

Format

CTD + COPP

Track

WHO Essential Medicines

LatAm · SEA

LatAm

ANVISA, COFEPRIS, INVIMA

SEA

BPOM, FDA PH, MOH VN

Format

CTD / ACTD

Get Started

Work With Coherence Scientific

📑

Request a Product or Dossier

Receive product availability, regulatory status, pricing, and your complete documentation package within a business day.

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🏢

Register as a Supplier or Partner

Gain access to established regulatory market channels across the USA, EU, MENA, and Southeast Asia. We review and respond within five business days.

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Join Our Team

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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