We provide a worldwide audit service to qualify suppliers, by rigorous audits to verify the compliance of regulatory requirements at the site of manufacturer.
We support to the companies to enhance the data management at their manufacturing site. Following ALCOA+ principle strictly to ensure the compliance status for data integrity at the manufacturing site.
we provide exceptional service to the Pharmaceutical companies to enrich the GMP compliance culture at the site and help to boost the confidence to remain GMP compliance always.
Our team has expertise to support due diligence of Pharmaceutical factory.
Support to find out the gaps between actual practices and written procedures at the site.
we extend our support Pre-audit, during audit, and Post audit to complete life cycle of regulatory inspection.
Internal audits of Pharmacovigilance Systems Support and assistance in inspections issued by the Health Authorities External audits of subsidiaries, partners and CROs In-person/remote audits
Internal audits, supplier qualification in line with ISO 13485
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