InstantGMP Blog | Good Manufacturing Practices

Controlled vs. Uncontrolled Documents in GMP

Controlled vs. Uncontrolled Documents in GMP...

Written by Dr. Richard Soltero, President, InstantGMP, Inc. GMP Document Control: Controlled vs. Unc...

Enhancing Documentation of Procedures for GMP Compliance

Enhancing Documentation of Procedures for GMP Compliance...

The Role of Documentation in GMP Compliance Good Manufacturing Practices (GMP) for pharmaceuticals...

InstantQMS Integration: One Platform for Total Quality

InstantQMS Integration: One Platform for Total Quality...

The Question Nobody Asks Until It Is Too Late Most quality teams I have worked with over the past 30...

Deviation Management: From Event to Evidence

Deviation Management: From Event to Evidence...

A deviation doesn’t end when the manufacturing line restarts. It ends when you can prove, with...

Document Control Done Right

Document Control Done Right...

A small manufacturer in Virginia received an FDA Warning Letter after an inspection revealed that pr...

CAPAs That Actually Close | InstantGMP QMS Workflow

CAPAs That Actually Close | InstantGMP QMS Workflow...

CAPAs That Actually Close How a Structured QMS Workflow Eliminates the Backlog If you have ever walk...

Small Team Big Compliance

Small Team Big Compliance...

You Don’t Need a Big Team to Have a Big Quality System When you’re running a small manufacturing...

GMP Software for Audit Readiness: How InstantGMP Simplifies ...

In regulated manufacturing industries, audit readiness is not optional — it is essential. Whether ...

Master Test Protocols versus Active Test Protocols in LIMS...

February 24, 2026

INSTANTGMP LIMS Master vs. Active Test Protocol: Why the Distinction Matters for Good Laboratory P...

Why Testing Is the Backbone of GMP Compliance

Why Testing Is the Backbone of GMP Compliance...

February 20, 2026

Ensuring GMP Compliance Through Effective Testing Testing is a cornerstone of Good Manufacturing Pra...