Last Updated
Overview
InstantGMP MES enables pharmaceutical and biotech manufacturers to maintain full compliance and traceability through electronic batch records, inventory control, and real-time production monitoring. While customization options are somewhat limited, it provides a secure, FDA-compliant solution ideal for small to mid-sized life science organizations seeking operational consistency and quality assurance.
Be the first one to leave a review!
No review found
Starting Price
$25,000
/year
InstantGMP MES Specifications
Production Planning
Inventory Management
Quality Control
Work Order Management
What Is InstantGMP MES?
InstantGMP MES is a cloud-based Manufacturing Execution System built to enforce FDA regulations and Good Manufacturing Practices (GMP). It provides an all-in-one solution for small-to-midsize manufacturers by seamlessly integrating Electronic Batch Records (EBR) with real-time inventory control and a complete Quality Management System (QMS). This unified platform streamlines operations, enhances traceability, and helps businesses replace inefficient paper-based systems to ensure end-to-end compliance.
InstantGMP MES Pricing
Disclaimer: The pricing has been sourced from third-party websites and is subject to change.
InstantGMP MES Integrations
Who Is InstantGMP MES For?
InstantGMP MES caters to businesses across various industries and sectors, such as:
- Biotechnology
- Chemical
- Manufacturing
- Pharma
Is InstantGMP MES Right For You?
InstantGMP MES is the right fit for small-to-midsize manufacturers in GMP-regulated industries who need to digitize operations and ensure compliance without the complexity and cost of enterprise-level systems. Its standout differentiator is that the software is ‘validated out of the box,’ saving companies the significant time and expense of a third-party validation project.
Still doubtful if InstantGMP MES is the right fit for you? Connect with our customer support staff at (661) 384-7070 for further guidance.
InstantGMP MES Features
This module creates and maintains 21 CFR Part 11 compliant electronic batch records. It enables version control for Master Production Records, ensures procedural enforcement for operators, and provides scalability and traceability with secure electronic signatures.
This feature enables precise, real-time tracking of all materials, from raw ingredients to finished goods. It documents every inventory transaction for full traceability, integrates with material planning, and incorporates user access controls to safeguard sensitive data.
A complete, built-in system for quality assurance and documentation. It manages deviations, corrective and preventive actions (CAPAs), complaints, and all quality-related workflows in a structured, easy-to-use format, ensuring compliance across all operations.
This system provides a central, secure repository for all critical company documents, including Standard Operating Procedures (SOPs). It ensures that all personnel have access to the latest approved versions, streamlining document control and review processes.
It digitizes the management of all facility and production equipment. Users can maintain comprehensive logs for cleaning, maintenance, and calibration, linking equipment status directly to batch records to ensure only qualified equipment is used.
Top Recommended Software
