When it comes to pharmaceutical manufacturing and regulatory compliance, accuracy in translation can mean the difference between approval and rejection. That’s why leading U.S. life sciences companies rely on Varendi — one of the most experienced Pharmaceutical Translation Companies providing world-class GMP Translation Services and Regulatory Document Translation solutions.

At Varendi, we understand that Good Manufacturing Practice (GMP) documentation is not just text — it’s a binding compliance record. Our expert translators specialize in gmp documentation translation, regulatory submissions translations, and pharmaceutical contract translation that meet FDA, EMA, and ISO standards. Whether you need translation for batch records, SOPs, CAPAs, or validation protocols, Varendi ensures technical precision and linguistic clarity every step of the way.

We also provide Certified Translation Services Portuguese, designed specifically for pharmaceutical companies expanding into Brazil and other Portuguese-speaking regions. Each translation is certified, regulator-approved, and delivered with guaranteed confidentiality.

In addition to GMP and regulatory content, Varendi offers Medical Device Translation services that align with EU MDR and U.S. FDA regulations. From IFUs and product labels to risk management and quality assurance documentation, we ensure every technical term is accurate and compliant.

With over three decades of experience in pharmaceutical document translation and technical translation services, Varendi stands at the intersection of science and language — helping U.S. companies succeed globally without compliance risks.

✅ Why Choose Varendi?

Certified translators with scientific backgrounds

Expertise in regulatory and GMP documentation

ISO 9001 and ISO 17100 certified processes

Multilingual support across 120+ languages

Secure and confidential translation workflows

📍 Location: Serving clients across the United States 🌐 Visit: https://varendi.com/ »

📞 Contact: info@varendi.com »