Varendi LLC, a leading provider of specialized language solutions for the life sciences sector, is proud to announce the expansion of its GMP Translation Services, supporting global pharmaceutical and biotech companies in maintaining compliance with international Good Manufacturing Practice (GMP) regulations.

As regulatory expectations grow more stringent and global supply chains become increasingly complex, Varendi LLC has developed a robust suite of GMP translation solutions tailored for regulatory, manufacturing, and quality assurance documentation. The company’s services help life sciences organisations navigate the highly regulated environments of the FDA, EMA, and other global health authorities.

“Our mission at Varendi LLC is to provide accurate, timely, and regulatory-compliant translations that meet the highest industry standards,” said Erica M. Varendi, CEO and Founder of Varendi LLC. “With our expanded GMP Translation Services, we aim to be the trusted language partner for pharmaceutical and biotech companies operating in multiple markets.”

Varendi LLC’s team of certified linguists and subject matter experts ensure that every translation—whether for batch records, SOPs, quality manuals, or validation reports—adheres to the strict terminology and formatting required by GMP protocols. The company also leverages advanced translation memory tools and rigorous quality control workflows to deliver consistency and precision across every project.

Key industries served include:

Pharmaceuticals

Biotechnology

Medical Devices

Clinical Research

This expansion reflects Varendi LLC’s ongoing commitment to innovation, compliance, and client satisfaction. By strengthening its GMP translation capabilities, the company continues to support global regulatory submissions, audits, inspections, and cross-border manufacturing operations.