InstantGMP™ Enhances Support for Latin American Manufacturers with Spanish Website Launch

InstantGMP™ Translates Site to Spanish for Enhanced Compliance in Latin America



InstantGMP™, a prominent name in electronic batch records and quality management, has taken a significant step towards supporting regulated manufacturers in the Spanish-speaking regions of the world. On February 24, 2025, the company announced the launch of a Spanish-language version of its website. This initiative aims to assist pharmaceutical, dietary supplement, and cannabis manufacturers across Spain, Mexico, and Latin America in complying with local regulations and international standards.

As the global demand for high-quality, good manufacturing practice (GMP) software rises, the addition of a Spanish version of the website is a proactive response to this growing market. Manufacturers can now explore InstantGMP’s intuitive digital solutions, which streamline operations and enhance regulatory compliance. By making the site available in Spanish, InstantGMP is focusing on bridging the compliance gap in Spanish-speaking markets, particularly in the pharmaceutical and dietary supplement sectors.

Regulated manufacturers in Spain must adhere to strict guidelines set out by the Spanish Agency of Medicines and Medical Devices (AEMPS), which enforces EudraLex Volume 4 regulations that govern GMP standards. In this context, the AEMPS is responsible for overseeing drug applications, conducting clinical trials, and performing GMP inspections to maintain industry standards consistent with EU and PIC/S regulations. The availability of InstantGMP’s software solutions in Spanish is a vital resource for companies looking to improve their compliance workflows through digital batch records.

Similarly, in Mexico, the Federal Commission for the Protection against Sanitary Risks (COFEPRIS) enforces stringent GMP regulations crucial for the country’s pharmaceutical manufacturing landscape. COFEPRIS's regulations include NOM-164 for pharmaceuticals and NOM-248 for dietary supplements, with GMP-certified facilities often being exempt from additional inspections. The new Spanish-language website empowers manufacturers in Mexico and other Latin American countries to gain access to the digital tools that simplify compliance and documentation processes.

Dr. Richard Soltero, President of InstantGMP, stated, “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.” He emphasized that these regions are witnessing rapid growth in regulated industries, highlighting the importance of digital solutions such as electronic batch records to help navigate the complex regulatory environment while bolstering operational efficiency.

The Spanish-language website features several key components designed to support GMP compliance:

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

Through this strategic enhancement, InstantGMP ensures that manufacturers throughout Spain, Mexico, and Latin America can now explore the full suite of GMP compliance software solutions in their native language, significantly improving accessibility and understanding of the tools needed for regulatory compliance.

For those interested in seeing these software products in action, InstantGMP encourages potential clients to reach out to their sales team for demonstrations and more information.

About InstantGMP™
Founded by industry expert Dr. Richard Soltero, InstantGMP, Inc. provides an affordable, all-in-one manufacturing, inventory, and quality software solution. The company specializes in creating cloud-based electronic batch record systems and standard operating procedures tailored to industries that must adhere to FDA regulations and GMP guidelines. With its user-friendly software, InstantGMP has been at the forefront of making GMP documentation efficient and accessible for a variety of manufacturing sectors.

Topics Consumer Technology)

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