Instantgmp Launches Spanish-Language Translation Of Website To Support Regulated Manufacturers In Spain, Mexico, And Latin America

CARY, N.C., Feb. 24, 2025 /PRNewswire/ -- InstantGMP™, a leading provider of electronic batch record (EBR), manufacturing execution system (MES), quality management system (QMS), and GMP compliance software for regulated industries, is proud to announce the launch of a Spanish-language translation of its website. This initiative will help pharmaceutical, dietary supplement, and cannabis manufacturers in Spain, Mexico, and Latin America comply with both the Spanish pharmaceutical regulatory authority and international standards, including COFEPRIS GMP standards, EMA guidelines, and FDA requirements.

InstantGMP launches a Spanish-language translation of its website to support regulated manufacturers in Latin America.

As the demand for high-quality, GMP-compliance software continues to grow across global markets, this new Spanish-language website enables more manufacturers to streamline operations, enhance regulatory compliance, and improve efficiency with InstantGMP's intuitive digital solutions.

With this new website enhancement, InstantGMP helps bridge the compliance gap for Spanish-speaking markets. Pharmaceutical and supplement manufacturers in Spain must adhere to Spanish pharmaceutical regulations outlined in EudraLex Volume 4 and enforced by the AEMPS (Agencia Española de Medicamentos y Productos Sanitarios or Spanish Agency of Medicines and Medical Devices).

The AEMPS oversees drug applications, clinical trials, and GMP inspections, aligning with EU and PIC/S (Pharmaceutical Inspection Convention and Pharmaceutical Inspection Co-operation Scheme) regulations to ensure consistent manufacturing standards. With InstantGMP's software solutions now available in Spanish, companies in Spain can improve their compliance workflows through digital batch records and automated quality management.

Similarly, in Mexico, COFEPRIS (Comisión Federal para la Protección contra Riesgos Sanitarios or Federal Commission for the Protection against Sanitary Risk) enforces stringent GMP guidelines, including NOM-164 for pharmaceutical manufacturing and NOM-248 for dietary supplements. COFEPRIS has also implemented certification processes for compliance, with GMP-certified facilities in reference countries exempt from additional inspections.

By providing InstantGMP's website in Spanish, regulated manufacturers in Mexico and Latin America now have greater access to digital solutions that simplify compliance and documentation.

"With the launch of our Spanish-language website, we are reinforcing our commitment to making compliance more accessible for pharmaceutical and dietary supplement manufacturers in Spain, Mexico, and Latin America," said Dr. Richard Soltero, President of InstantGMP. "These regions have rapidly expanding regulated industries, and we recognize the need for digital solutions such as electronic batch records for manufacturers that help companies navigate complex regulatory landscapes while improving operational efficiency."

InstantGMP's Spanish-language website ensures that more manufacturers can easily explore features such as:

Electronic Batch Record (EBR) and Manufacturing Execution System (MES) modules designed for GMP compliance.
Automated quality management workflows to streamline documentation.
Cloud-based solutions for secure, real-time access to production data.
Paperless record-keeping that meets FDA, EMA, and COFEPRIS standards.

Manufacturers across Spain, Mexico, and Latin America can now explore InstantGMP's full suite of GMP compliance software solutions in Spanish.

To learn more, contact our sales team today to schedule a demonstration of InstantGMP's software products.

About InstantGMP™, Inc.

Founded by pharmaceutical industry veteran Dr. Richard Soltero, InstantGMP, Inc., offers affordable all-in-one manufacturing, inventory and quality software. The company develops cloud-based electronic batch record software and standard operating procedures specific to industries that are required to follow FDA manufacturing regulations and Good Manufacturing Practices ("GMP").

As a manufacturing software company, InstantGMP™ pioneered accessible, easy-to-use electronic batch record software for products manufactured using GMPs. The Company's updated software simplifies the documentation and approval procedures for quality processes that keep all quality documentation organized in electronic format while providing for quality checks and workflow processes to make compliance with FDA requirements easy.

View original content to download multimedia:https://www.prnewswire.com/news-releases/instantgmp-launches-spanish-language-translation-of-website-to-support-regulated-manufacturers-in-spain-mexico-and-latin-america-302382348.html

SOURCE InstantGMP, Inc.

First published on Tue, Feb 25, 2025

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