Guides for EU procurement, QA and regulatory teams sourcing ingredients from India.https://gfclinics.pl/en-gbhttps://gfclinics.pl/insights/cep-vs-asmf-api-documentation/https://gfclinics.pl/insights/cep-vs-asmf-api-documentation/A CEP is an EDQM certificate confirming that the Ph. Eur. monograph controls one manufacturer's substance. An ASMF is a confidential file the authority assesses with each application. Both support Module 3. Neither replaces the buyer's own checks on GMP, impurities and import papers.Sat, 17 Oct 2026 00:00:00 GMThttps://gfclinics.pl/insights/ethylene-oxide-testing-indian-botanicals/https://gfclinics.pl/insights/ethylene-oxide-testing-indian-botanicals/Ethylene oxide residues are measured as the sum of ethylene oxide and 2-chloroethanol. EU limits sit at the limit of quantification. As of October 2026, many Indian spices and botanical food-supplement ingredients still need an official certificate and lab report at the EU border.Sat, 17 Oct 2026 00:00:00 GMThttps://gfclinics.pl/insights/indian-api-import-documentation-checklist/https://gfclinics.pl/insights/indian-api-import-documentation-checklist/An API from India needs evidence of EU GMP, a CEP or ASMF, and a written confirmation from India's regulator. Each batch needs a specification and certificate of analysis. In Poland, the importer registers with GIF and follows EU GDP for active substances.Sat, 17 Oct 2026 00:00:00 GMT