#United States #CARY #Latin America #InstantGMP #GMP Compliance

InstantGMP's Commitment to Latin America

In a significant move to bolster its presence in Latin America, InstantGMP™ has announced the launch of its Spanish-language software and customer support initiatives. This strategy aims to assist pharmaceutical and supplement manufacturers in Spanish-speaking countries, enabling them to navigate the complexities of regulatory compliance effectively.

A Step Towards Inclusivity

The highlight of this outreach effort includes a recent video interview featuring Angelo Nardone, the Chief Technology Officer of InstantGMP, as showcased in Cosmetic Latam®. This platform is integral for professionals in the Latin American cosmetics and pharmaceutical industries. During the discussion, Nardone emphasizes the significance of compliance software that is now fully localized in Spanish. This enhancement allows manufacturers in countries like Mexico, Colombia, Chile, and Argentina to meet the stringent regulatory requirements of agencies such as COFEPRIS and INVIMA.

Localized Software and Customer Engagement

With the launch of the Spanish-language website, InstantGMP provides straightforward access to its solutions including electronic batch records and integrated quality systems tailored to comply with both COFEPRIS GMP standards and FDA regulations. The user-friendly interface is designed for easy onboarding and effective communication with Spanish-speaking clients, ensuring that they can utilize the tools necessary for efficient manufacturing practices.

Moreover, InstantGMP made a pivotal addition to its team by appointing Tar St. Martin as the new Director of Sales. Fluent in Spanish and possessing extensive knowledge of regulated manufacturing, St. Martin is tasked with enhancing customer engagement in Latin America. He will assist clients throughout the process, from initial consultations to software implementation and training, ensuring that language is no longer a barrier to compliance.

Overcoming Challenges in Regulated Markets

InstantGMP's President, Dr. Richard Soltero, remarks, "Navigating compliance in Latin America can be complicated due to overlapping regulatory frameworks." To address this, InstantGMP aims to simplify these processes through its cloud-based solutions that offer secure and real-time access to critical production data. The commitment to developing accessible and comprehensive solutions sets the foundation for creating a more inclusive and efficient operational experience for international clients.

Features to Note

The Spanish-language offerings promise significant advantages, including:

• - Electronic Batch Records (EBR) and Manufacturing Execution Systems (MES) customized for GMP compliance.
• - Streamlining quality management workflows through automated documentation processes.
• - Paperless record-keeping aligned with the standards of the FDA, EMA, and COFEPRIS.

This initiative opens the door for manufacturers across Latin America to explore a complete suite of GMP-compliant software solutions in their native language. Interested parties can contact InstantGMP's sales team for demonstrations and further information on how these tools can benefit their operations.

About InstantGMP™

Founded by industry expert Dr. Richard Soltero, InstantGMP, Inc. provides an all-in-one solution for manufacturing, inventory, and quality management tailored for the pharmaceutical sector. Their cloud-based software adheres to FDA manufacturing regulations and Good Manufacturing Practices (GMP). InstantGMP aims to streamline quality documentation processes, making compliance and operational efficiency straightforward and hassle-free for its users.

In conclusion, InstantGMP’s latest expansion serves not only to strengthen its foothold in Latin America but also ensures that Spanish-speaking manufacturers are equipped with the necessary tools to comply with industry standards effectively. The commitment to inclusivity is evident as InstantGMP continues to innovate and grow within the pharmaceutical landscape.