#CARY #InstantGMP #EBR #LIMS

InstantGMP Earns Recognition for EBR Integration

InstantGMP™, a software solution designed specifically for GMP-regulated manufacturers, has recently achieved a significant milestone by being named the top provider of Electronic Batch Record (EBR) integration by Root Analysis Business Research & Consulting. This commendation highlights InstantGMP's exceptional capabilities within both Laboratory Information Management Systems (LIMS) and Manufacturing Execution Systems (MES), aiding the transition to fully paperless manufacturing.

Overview of the Recognition

According to an article released by Root Analysis, a trusted name in market research within the pharmaceutical and technology sectors, InstantGMP stands out as the premier software provider in terms of EBR functionalities. The report emphasizes InstantGMP's comprehensive suite of software solutions which align with strict FDA guidelines while also streamlining the manufacturing processes.

The Strength of InstantGMP’s Integrated Software

What sets InstantGMP apart is its natively integrated Laboratory Information Management System (LIMS). Unlike conventional LIMS systems that operate in isolation, InstantGMP’s LIMS is embedded within the manufacturing platform, creating a seamless connection with inventory management and electronic batch records. This integration ensures that all data related to quality control testing and production workflows is synchronized, maintaining data integrity throughout the product lifecycle.

Key Features of InstantGMP LIMS:

1. Deep GMP-Centric Integration: InstantGMP’s quality control (QC) module is attached to inventory, EBR, and sampling processes, ensuring that data remains consistent and audit-ready.
2. Master Test Protocol and Active Test Protocol Framework: This two-level system allows for standardized protocols that facilitate compliance during production, ensuring full version control and digital traceability.
3. Rich Test Result Capabilities: InstantGMP LIMS supports diverse testing formats such as qualitative and quantitative assessments, automatically linking results to Certificates of Analysis.
4. Dynamic Links to Specifications: Test protocols are maintained in real-time, ensuring compliance with approved product specifications.
5. Automated Certificates of Analysis (COAs): COAs generated through QC data include detailed test results, ensuring departmental compliance with FDA regulations.

Enhancing Paperless Manufacturing

InstantGMP’s commitment to paperless manufacturing is manifested through its innovative integration. As Dr. Richard Soltero, the company's president, stated,