ISO-Certified GMP Translations for Pharma Companies
Avoid regulatory delays and costly errors with Varendi’s ISO-certified GMP translation services. Translating SOPs, batch manufacturing records, validation protocols, and other regulatory documents, Varendi ensures precision, confidentiality, and strict compliance with international GMP standards.
Every translation is performed by industry-specific linguists and undergoes multistage quality control, guaranteeing clarity, accuracy, and compliance for submission to authorities such as the FDA, EMA, and PMDA. This rigorous process provides companies with peace of mind that their documentation is fully audit-ready.
Partnering with Varendi allows pharmaceutical and biotech companies to streamline regulatory submissions, mitigate compliance risks, and safeguard product quality globally. Their expertise supports international expansion while ensuring that patient safety and regulatory requirements remain uncompromised.