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The quality experts of InstantGMP, Inc. will be holding a webinar about changing from paper-based systems to electronic manufacturing for FDA regulated products. Registration is free until 10/1 by using the code earlybird! Take a look at our special preview video.
Why You Should Attend
  • Learn about how paper cause inefficiencies, errors, cross-departmental miscommunications, and avoidable redundancies
  • We will answer the most important questions about how to make the move
  • Each topic has been thoughtfully curated on how to build and champion the case for stakeholders and management
  • We’ll help you define expectations, challenges associated with moving, overlaying your production process on an electronic solution, and much more
  • Each attendee will leave educated and empowered about Electronic Batch Records
  • A special self-audit worksheet will be given to each attendee. This self-audit is not available to the public normally and was written by our own cGMP and quality experts
Areas Covered in the Seminar:
  • Goals: Defining your Expectations
  • Challenges in Making the Transition
  • Departmental Responsibilities
  • Self-Audit and Mapping Your GMP Workflow Process
  • Requirements and Design for an Electronic Solution
  • Overlaying Your Process on an Electronic Solution
Who Should Attend
  • Management
  • Directors and Managers from Operations, Production, and Quality
  • Quality Assurance
  • Line Management
  • Production
  • Operations
Join us for this highly-interactive 90-minute webinar.
Topic:  Changing from Paper-Based Systems to Electronic Manufacturing for FDA Regulated Products
Date: October 4th, 2016, Tuesday
Time: 2pm EDT – Duration: 90 Minutes
Location: Live, interactive training on your computer
Includes proprietary tools and helpful documentation!
Register Now (use code earlybird before 10/1 to register for free)


About InstantGMP, Inc.:
InstantGMP, Inc. is the brain-child of Dr. Richard Soltero. Dr. Soltero created InstantGMP™ MES after being unable to find a sufficient software system that would comply with regulations and help streamline the manufacturing process of pharmaceuticals.
Today, the software has grown and evolved to help those in many industries comply with their regulations or simplify their production process. With a full suite of Standard Operating Procedures,software, consulting, and more, the experts at InstantGMP, Inc. can help your organization take their quality to a new level without breaking the bank.
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