Parallel importing (PI) and repackaging of pharmaceuticals and medicinal products requires the importer or re-packager to comply with pharmaceutical manufacturing rules and guidelines. They must conform to the GMP requirements of the country of origin and may require labels in languages other than English.
Our PS9000:2011 accreditation assures you of our capability of meeting these GMP requirements, and providing you with fast, cost-effective, high-quality labelling solutions. To guarantee label quality, our EyeC Proofiler inspection system compares the scanned label samples against the signed-off proof (typically a PDF file) ensuring that all the labels meet your requirements.
Sincerely Pharmaceutical Tech
Regards,
Client Success Team (CRM),
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Sincerely Packaging Labelling