keyhan daroo
Drug Product
Excipients & Specialty Ingredients
Analytical & Bioanalytical Services
Contract Research Organization
Qualification/Validation Services
Drug Substance
Consultants & Advisory Services
Company Overview
About
Keyhan Daroo is an agile and innovation-driven pharmaceutical technical services and consulting enterprise dedicated to delivering high-quality development, formulation, and quality compliance solutions. We specialize in transforming laboratory-scale chemical synthesis into robust, commercial-ready pharmaceutical products, with a core focus on solid dosage forms (tablets and capsules) and Active Pharmaceutical Ingredients (APIs). Operating with a strong commitment to international standards, Keyhan Daroo provides comprehensive support in establishing and optimizing Quality Assurance (QA) and Quality Control (QC) systems. Our technical capabilities include advanced in-vitro dissolution profiling, process engineering utilizing modern mini-reactor systems, and executing smooth technology transfers. Driven by a team of experienced pharmacists and chemical engineers, we help our global partners navigate complex CMC requirements, upgrade manufacturing facilities to meet strict PIC/S and EU GMP guidelines, and ensure total regulatory readiness. At Keyhan Daroo, we bridge technical precision with scalable pharmaceutical excellence.
Therapeutic Areas
Infectious Disease
Quick Facts
HQ:United Kingdom
Employees:125
Consulting Services
Expert Pharmaceutical Consulting: GMP, PIC/S Compliance & Analytical Laboratory Services. Full-Scale Formulation Development, Tech Transfer & Solid Dosage Operations Consulting
Drug Development & Formulation
We are a premier pharmaceutical technical services and consulting organization specializing in end-to-end solutions for drug development, manufacturing operations, and strict quality compliance. Led by an experienced industry administrator, our team bridges the gap between laboratory-scale synthesis and commercial production. Our core expertise encompasses: • Quality & Regulatory: Comprehensive support in establishing, upgrading, and auditing Quality Assurance (QA) and Quality Control (QC) systems aligned with PIC/S, EU GMP, and ICH guidelines (including Q1 stability and Q7 GMP standards). • Formulation & Analytics: Advanced product development for solid dosage forms (tablets and capsules), manufacturing process optimization, and comparative in-vitro dissolution testing against global reference brands. • Process Engineering & Tech Transfer: Technical management of laboratory scale-ups, utilizing mini-reactor technologies, and conducting rigorous technical evaluation of chemical synthesis (e.g., Active Pharmaceutical Ingredients). We empower pharma and biotech companies worldwide by streamlining their tech transfer, ensuring regulatory readiness, and optimizing laboratory operations through data-driven, compliant methodologies.
- Industry experience
- 19 years
- Engagement types
- consulting
Capabilities & Services
Core Capabilities
- Microbiology Testing
- Method Development & Validation
- Stability Studies
Types of Organization
Formulation Development
Dosage Forms
Oral Solid Dose
Containment Capabilities
None Required
Production Scales
R&D / Pre-clinical
Pilot Scale
Commercial Scale
Annual Capacity
Commercial (10,000-100,000 units/year)
Medium Clinical (1,000-10,000 units/year)
Markets Served
Middle East
Asia Pacific
Europe
Certifications
GMP (Good Manufacturing Practice)
Various National Authorities