Operator using the InstantGMP Software System, ranked in the Top 8 for GMP Software Solutions

“It’s always an honor to be recognized by our peers for our contributions to supporting Good Manufacturing Practices,” said Dr. Richard Soltero, President of InstantGMP.

CARY, N.C. (PRWEB)
July 25, 2022

InstantGMP announced today that its InstantGMP PRO, the only all-in-one manufacturing and quality system, has been named one of the Eight Best GMP Software Solutions for 2022.

With this honor, InstantGMP, an internationally recognized leader in MES software solutions, now stands alongside other prominent GMP software providers as a pioneer in the industry.

All of the GMP software on this list were selected based on their outstanding performance and features that allow manufacturers to achieve and manage good manufacturing practices efficiently and effectively. While many of these products specialize in specific areas of GMP manufacturing such as risk assessment and enterprise resource planning, InstantGMP is the only all-in-one system.

After thoroughly evaluating each GMP software solution, InstantGMP PRO’s high marks were based its capacity to provide GMP manufacturers with an all-in-one software solution that includes the following modules:

• 
  Electronic Batch Records (EBR): Simplifies developing, producing and identifying Master Batch Records (MBR) and Batch Production Records (BPR) to enhance quality control, improve workflow management, and increase safety.
• Quality Management System (QMS): Supports quality assurance activities, controls all necessary documentation for deviation tracking, root cause identification and investigations, and manages the required specifications for verifying incoming raw materials and outgoing finished products.
• Inventory Management: Traces, monitors and records every step of the inventory process from ordering raw material to final production.
• Document Management System (DMS): Stores, organizes and secures access to all production files, records and videos. Promptly locates documents for review, updates and approvals during every step of production.
• Learning Management System (LMS): Assigns coursework to new and existing employees and uploads certifications to the respective employee files.

In addition to the above benefits, InstantGMP PRO rates high on the list of best GMP software for its user-friendly design and affordability (ideal for small and mid-size enterprises). Plus, it’s pre-validated to save time and money when implementing the system.

“It’s always an honor to be recognized by our peers for our contributions to supporting Good Manufacturing Practices,” said Dr. Richard Soltero, President of InstantGMP. “With InstantGMP PRO, we supply manufacturers with an all-in-one software that introduces efficiencies and improvements to their processes via make-to-order batch record creation, enhanced internal processes, greater client oversight and participation, first-rate inventory and document management, and out-of-the-box validation. As a result of all of these software features, InstantGMP PRO helps facilities maintain GMP compliance to manufacture safe, high-quality products.”

To learn more about our industry-leading InstantGMP PRO software, please contact us today to schedule a live demonstration.

About InstantGMP™, Inc.

Founded by pharmaceutical industry veteran Dr. Richard Soltero, InstantGMP Inc., offers affordable all-in-one manufacturing 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.

Share article on social media or email: