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InstantGMP Enhances 5-Point Implementation Plan

InstantGMP™, a recognized leader in GMP-compliant manufacturing software designed for pharmaceutical and regulated industries, has recently announced significant enhancements to its 5-Point Implementation Plan. The upgraded plan now includes expanded on-site services tailored to help manufacturers achieve a faster return on investment (ROI), streamline the adoption of systems, and ensure readiness for Good Manufacturing Practices (GMP) and FDA compliance.

The newly revamped 5-Point Implementation Plan offers a systematic approach for integrating customers into the InstantGMP™ PRO manufacturing execution system and electronic batch records. This refined strategy is grounded in valuable feedback from clients and extensive industry experience, providing each organization with guided support, expert training, and essential tools for sustained operational success.

On-Site Implementation Services

A noteworthy feature of the improved implementation plan is the focus on on-site support. By offering on-site implementation, InstantGMP provides several advantages for manufacturers eager to maintain project momentum and enhance accuracy during system setup. With this hands-on approach, teams can transition from the planning phase to execution more effectively than ever before.

Key Benefits of On-Site Implementation

1. Increased Project Commitment: When customers arrange an in-person visit for implementation, their internal teams are likely to dedicate more focused time to onboarding tasks. This commitment helps avoid project delays caused by conflicting operational priorities.

2. Customized Training: While virtual training sessions offer some benefits, many teams learn better with direct, hands-on instruction. On-site visits allow InstantGMP trainers to teach processes and implement software functionalities in real time, leading to improved understanding and quicker proficiency.

3. Deep Understanding of Operations: By observing a facility's workflow and equipment layout directly, InstantGMP can better grasp each customer's unique challenges. This understanding enables more accurate system configurations from the outset, significantly reducing the need for corrections, re-entries, or adjustments down the line.

4. Real-Time Collaboration: On-site interactions foster immediate communication between InstantGMP experts and customer teams, ensuring questions can be addressed, steps can be validated, and issues can be resolved without the delays that sometimes accompany virtual meetings.

5. Efficient Record Setup: Certain implementation tasks—like creating Master Production Records (MPRs) and Master Test Protocols (MTPs)—can be executed much faster with InstantGMP experts on-site. This efficiency is particularly beneficial for complex formulas that involve detailed calculations or intricate processes, allowing teams to work in parallel.

As Brandy Irons, Senior Training and Technical Support Manager/Quality Assurance at InstantGMP, remarks, “Being on-site provides us with a clearer perspective on each customer's distinct processes. This insight allows us to configure their systems correctly from the beginning, facilitating better training, communication, and collaboration, which ultimately helps teams to get operational more swiftly with InstantGMP.”

Integration with the 5-Point Plan

The enhanced on-site services work seamlessly within InstantGMP's original 5-Point Implementation Plan, consisting of:

• - Phase 1: Planning & System Design
• - Phase 2: System Configuration & Implementation
• - Phase 3: Pilot Testing, Operator Training & System Launch
• - Phase 4: Optimization
• - Phase 5: Ongoing Configuration Assistance

This structured implementation strategy aligns with GMP and FDA compliance requirements, transforming system adoption into a measurable and guided process.

To explore more about InstantGMP's enriched on-site services and the 5-Point Implementation Plan, interested parties are encouraged to reach out to their sales team today.

About InstantGMP™

Founded by industry expert Dr. Richard Soltero, InstantGMP, Inc. provides comprehensive, cloud-based manufacturing, inventory, and quality software tailored for enterprises that need to adhere to FDA regulations and Good Manufacturing Practices (GMPs). This software facilitates an organized approach to documentation and approval processes in regulatory compliance, thereby streamlining procedures for quality management across the board.