InstantGMP™, a top provider of software for pharmaceutical as well as regulated industries, has improved its 5-Point Implementation Plan by adding on-site services to help customers get faster return on investment (ROI), streamline system adoption, and speed up GMP (Good Manufacturing Practice) and FDA compliance.
The 5-Point Implementation Plan gives a clear, step-by-step guide for customers to initiate using InstantGMP™ PRO, a software system for managing manufacturing processes as well as batch records. This plan is based on feedback from customers and years of expertise, ensuring that companies get the support, training, as well as the tools they require to succeed in the long run.
Now, InstantGMP is enhancing this plan by offering on-site implementation services, which provide several benefits:
- Faster project progress and reduced delays
- Customized training for different learning styles
- A better understanding of how the facility works
- Real-time collaboration with full focus
- Quicker setup of complex manufacturing records
This new approach helps teams move quickly from planning to execution with more confidence and efficiency.
InstantGMP was founded by Dr. Richard Soltero, a veteran in the pharmaceutical industry. The company provides affordable, all-in-one pharmaceutical software for manufacturing, inventory, and quality control. They create cloud-based software for electronic batch records and standard operating procedures, specifically designed for industries that must follow FDA regulations and Good Manufacturing Practices (GMP).
Executive Statement
According to Brandy Irons, Senior Training and Technical Support Manager/Quality Assurance at InstantGMP, being on-site gives them a clearer understanding of each customer's unique processes, which means they can configure their system correctly the first time. It also reinforces training, communication, and collaboration, which in turn helps teams get up and running faster with InstantGMP.
