keyhan daroo

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.