InstantGMP Launches 5-Point Implementation Plan for Software Success

CARY, N.C., April 16, 2025 /PRNewswire/ — InstantGMP™, a leading provider of GMP-compliant software solutions for pharmaceutical and regulated manufacturing, is proud to announce the launch of its 5-Point Implementation Plan, a strategic, streamlined onboarding process designed to help new clients achieve GMP success faster and more effectively.

The new 5-Point Implementation Plan is based on years of hands-on experience and direct feedback from clients across the pharmaceutical, biotech, dietary supplement, and cannabis industries. This structured approach to manufacturing software implementation provides a clear roadmap that ensures each customer, regardless of their starting point, receives the support, guidance, and tools needed to unlock the full potential of the InstantGMP™ PRO pharmaceutical manufacturing software.

“The best software won’t deliver results without the right implementation behind it,” said Dr. Richard Soltero, President of InstantGMP. “We designed our implementation plan to be collaborative, customizable, and comprehensive so that our customers feel confident and in control from day one.”

The 5 Phases of the Implementation Plan include:

• Phase 1: Planning & System Design: A virtual kick-off meeting to define scope, goals, responsibilities, and project timelines.
• Phase 2: System Configuration & Implementation: On-site configuration of inventory, equipment, documents, and LMS curricula, including MPR entry and testing.
• Phase 3: Pilot Testing, Operator Training & Launch: On-site pilot project selection, training for operational and quality roles, and live rollout with performance monitoring.
• Phase 4: Optimization: Virtual meetings to optimize workflows, refresh training, and fine-tune system functionalities.
• Phase 5: Ongoing Configuration Assistance: Continued support, virtually or on-site, including assistance with dynamic fields, scale integrations, or operational resets.

By combining expert-led training, live collaboration, and on-demand assistance, this implementation plan transforms software adoption into a structured, manageable, and measurable process that helps manufacturers meet FDA and GMP compliance standards while maximizing operational efficiency.

To learn more about InstantGMP’s 5-Point Implementation Plan and how it can benefit your manufacturing operations, contact our sales team today.

About InstantGMP™, Inc.

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

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SOURCE InstantGMP, Inc.