CARY, N.C., March 24, 2025 -- 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 excited to announce that its flagship software, InstantGMP PRO™, is now available in Spanish. Following the recent launch of a Spanish-language translation of the InstantGMP website, this major development will enable pharmaceutical, dietary supplement, and cannabis manufacturers in Spain, Mexico, and Latin America to streamline their compliance efforts with digital solutions tailored to their language needs.
With the increasing demand for advanced manufacturing solutions that meet global regulatory requirements, the availability of InstantGMP PRO™ in Spanish ensures that manufacturers can efficiently manage Registro de Producción de Lote (Batch Records), optimize Gestión de Calidad (Quality Management), and improve Gestión de Inventario (Inventory) through an intuitive, all-in-one system.
Compliance with Good Manufacturing Practices (GMP) is essential for pharmaceutical and dietary supplement manufacturers worldwide. In Spain, manufacturers must adhere to EudraLex Volume 4 and AEMPS (Agencia Española de Medicamentos y Productos Sanitarios) regulations, while in Mexico, COFEPRIS (Comisión Federal para la Protección contra Riesgos Sanitarios) enforces GMP guidelines such as NOM-164 for pharmaceutical products and NOM-248 for dietary supplements.
With InstantGMP PRO™ now available in Spanish, companies in these regions can enhance compliance processes, reduce errors, and improve operational efficiency by utilizing automated workflows. The cloud-based software's comprehensive features support manufacturers in maintaining regulatory compliance while 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 equipping manufacturers in Spain, Mexico, and Latin America with the tools they need to enhance efficiency, meet GMP standards, and compete in the global market."
Key Features of InstantGMP PRO™ in Spanish:
- Registro de Producción de Lote (Batch Records): Electronic batch record creation and management ensures data accuracy, compliance, and traceability.
- Gestión de Calidad (Quality Management): Automated workflows streamline compliance documentation and reduce the risk of errors.
- Gestión de Inventario (Inventory): Real-time inventory tracking and control to optimize production efficiency.
- Cloud-Based Access: Secure, real-time data accessibility from anywhere, enabling seamless remote operations.
- Paperless Compliance: Eliminate manual paperwork while adhering to FDA, EMA, and COFEPRIS regulations.
By providing InstantGMP PRO™ in Spanish, InstantGMP is ensuring that regulated manufacturers in Spanish-speaking markets have the tools they need to modernize their production processes, maintain compliance, and drive business growth.
To see InstantGMP PRO™ in action and learn how it can support your compliance efforts, contact our sales team today to schedule a demonstration.
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.
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