Drug Logix India operates as a seamless extension of your R&D team. Whether you need a quick feasibility study, a multi-month impurity isolation project, or end-to-end chemistry outsourcing — our chemists deliver regulatory-grade work under signed confidentiality, tracked with weekly milestones and delivered with full spectral packages.
We partner with innovator pharma, generic formulators, biotech start-ups and academic collaborators — providing the bench-level execution, analytical depth and regulatory documentation every R&D engagement demands.
Start a CRO ProjectLiterature mining, retrosynthetic analysis, and feasibility-scale benchwork to de-risk your target molecule before committing to a route.
Yield improvement, solvent minimisation, impurity control and purity enhancement for smooth commercial-scale transfer.
Isolation, synthesis and ICH-grade characterisation of process, degradation and forced-degradation impurities.
HPLC, GC, LC-MS method development and validation to ICH Q2 standards, with full dossier-ready documentation.
Forced degradation under acid, base, oxidative, thermal and photolytic conditions — ICH Q1A-aligned stability studies.
Dossier-ready COAs, NMR/Mass/IR spectra, and ICH Q3A/Q3B impurity profiles for global regulatory submissions.
It's a project-management problem, a communication problem, and an audit problem. We handle all four — so your team can stay focused on what matters.
We are committed to excellence in pharmaceutical research, proudly holding certifications and accreditations that ensure the highest standards of quality, environmental responsibility and scientific integrity in our work.
Environmental Management System
Certified
Quality Management System
Certified
UKAF Accreditation
Accredited