InstantGMP PRO software is now available in Spanish, helping manufacturers in Latin America optimize processes for GMP compliance.
“Expanding InstantGMP to Spanish-speaking users reinforces our commitment to making compliance more accessible for manufacturers worldwide,” said Dr. Soltero, President.
— Dr. Richard Soltero
CARY, NC, UNITED STATES, April 14, 2025 / EINPresswire.com / -- InstantGMP™, a leading provider of Electronic Batch Records (EBR), Manufacturing Execution Systems (MES), Quality Management Systems (QMS), and GMP compliance software for regulated industries, is pleased to announce that
its flagship software, InstantGMP PRO™, is now available in Spanish. Following the recent launch of the Spanish version of its website, this important development will enable pharmaceutical, dietary supplement, and cannabis manufacturers in Spain, Mexico, and Latin America to streamline their compliance processes with digital solutions tailored to their language needs.With the growing demand for advanced manufacturing solutions that meet global regulatory requirements, the availability of InstantGMP PRO™ in Spanish ensures that manufacturers can efficiently manage the Production Batch Record , optimize Quality Management, and improve Inventory Management through an intuitive, fully integrated system in a single product.
Compliance with Good Manufacturing Practices (GMP) is essential for pharmaceutical and dietary supplement manufacturers worldwide. In Spain, manufacturers must comply with EudraLex Volume 4 and AEMPS (Spanish Agency for Medicines and Health Products) regulations, while in Mexico, COFEPRIS (Federal Commission for the Protection against Health Risks) enforces GMP guidelines such as NOM-164 for pharmaceutical products and NOM-248 for dietary supplements.
With InstantGMP PRO™, available in Spanish, companies in these regions can improve their compliance processes, reduce errors, and increase operational efficiency through automated workflows. The cloud-based software's comprehensive features support manufacturers in maintaining regulatory compliance by simplifying documentation and production management.
“Expanding InstantGMP PRO™ to Spanish-speaking users reinforces our commitment to making compliance more accessible for manufacturers worldwide,” said Dr. Richard Soltero, President of InstantGMP. “By offering our industry-leading software in Spanish, we are providing manufacturers in Spain, Mexico, and Latin America with the tools necessary to improve efficiency, comply with GMP standards, and compete in the global marketplace.”
Key Features of InstantGMP PRO™ in Spanish:
✅ Batch Production Log: Electronic creation and management of batch records ensures data accuracy, compliance, and traceability.
✅ Quality Management: Automated workflows that streamline compliance documentation and reduce the risk of errors.
✅ Inventory Management: Real-time inventory tracking and control to optimize production efficiency.
✅ Cloud-Based Access: Secure, real-time data accessible from anywhere, enabling seamless remote operations.
✅ Paperless Compliance: Eliminate manual documentation while meeting FDA, EMA, and COFEPRIS requirements.
By providing InstantGMP PRO™ in Spanish, InstantGMP ensures that regulated manufacturers in Spanish-speaking markets have the tools they need to modernize their production processes, maintain regulatory compliance, and promote business growth.
To see InstantGMP PRO™ in action and learn how it can support your compliance efforts, contact us today to schedule a demo.
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About InstantGMP™, Inc.
Founded by pharmaceutical industry veteran Dr. Richard Soltero over 20 years ago, InstantGMP, Inc. offers affordable, all-in-one manufacturing, inventory, and quality management software. The company develops cloud-based electronic lot record software and industry-specific standard operating procedures for industries that must comply with FDA manufacturing regulations and Good Manufacturing Practices (GMP).
As a manufacturing software company, InstantGMP™ pioneered the development of affordable, easy-to-use electronic lot record software. Its updated software simplifies documentation and approval procedures for quality processes by organizing all documentation into an electronic format while enabling quality checks and workflows that facilitate compliance with FDA requirements.
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