Expert knowledge on pharmaceutical chemical sourcing, procurement strategy, regulatory affairs, and supply chain management - from a team with 20+ years in the industry.
Which documents need apostille or legalisation before export - CoPP, FSC, WHO-GMP certificates, DMFs, Manufacturing Licences and commercial contracts. Step-by-step process via PHD Chamber and the Ministry of External Affairs.
Read Article →A reference directory of 120+ embassies and high commissions in New Delhi organised by region - covering Europe, Americas, Asia Pacific, Middle East and Africa - with guidance on document legalisation for each country.
Read Article →A practical framework for evaluating specialty chemical suppliers in pharma - covering regulatory compliance, documentation quality, supply reliability, and red flags to watch for.
Read Article →A complete guide to pharmaceutical raw material and API registration in India - covering CDSCO pathways, Drug Master Files (DMFs), import licences, and timelines.
Read Article →A guide to the world's top chemical sourcing destinations covering strengths, challenges, and sourcing strategy for Indian pharma procurement teams.
Read Article →A practical step-by-step guide to sourcing Active Pharmaceutical Ingredients (APIs) and bulk drugs - covering specifications, vendor qualification, and import documentation.
Read Article →A chemical indenting house bridges buyers and manufacturers for pharmaceutical raw materials - handling sourcing, compliance, logistics, and documentation. Learn how it works.
Read Article →Our team has sourced chemicals for 50+ pharma companies across India and internationally. Tell us what you need.
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