In-House Compliance Without the Big Expense

Standard NetSuite software can accommodate generic manufacturing solutions; however, it’s not ideal for pharmaceutical and biotech spaces. By enhancing basic NetSuite software with our industry-specific solutions, we’ve created a scalable platform that has all the tools necessary for a GMP-compliant process.

Key Features

Vendor and Materials Onboarding
Vendor/Material Onboarding
AdaptaLogix’s system is deployed with approved vendors and materials lists, to keep onboarding simple.
Purchasing Process
Purchasing Process
From APIs to secondary packaging, new equipment, and miscellaneous lab equipment, all purchases are automatically logged by their class, associated trial, and candidate. Easily run reports and maintain complete control over every department’s purchasing.
Inventory Management
Inventory Management
When physically on-hand inventory is recorded in a purchase receipt, materials are quarantined and a lot inspection process is started automatically with our supply-chain solutions. Inventory movements are limited by status, and automated processes for lot disposition are built in. All movements are recorded and exhibited via dashboards and alerts.
Sample Management
Sample Management
Take advantage of a centralized repository for managing all inventoried samples, including source, storage, and shipment to outside facilities.
Batch Management
Batch-Release Management
A formal release process captures all of the relevant data and documentation for final batch release.
GMP System Validation
GMP System Validation
All of the documentation needed for validation is already written, and upon delivery of your system, our team will help your organization complete and record the system testing.
Barcoding and WMS
Barcoding and WMS
AdaptaLogix provides everything an organization might need in its facility plus an integrated WMS system, from labels to handheld devices and printers.
Final Product Release/Material Lot Inspection
Final Product Release/Material Lot Inspection
Every lot of raw materials received or product produced for GMP manufacturing requires a review. AdaptaLogix’s system captures all relevant data and documentation and adheres to 21 CFR Part 11/Annex 11 requirements in the lot release process.
Security Configuration
Security Configuration
The FDA's 21 CFR Part 11 requires companies to validate their electronic systems and documents for quality and compliance. Automated solutions are most effective for this, and AdaptaLogix provides automatic 21 CFR Part 11 compliance, personnel training, and auto-generated audit trails for any captured document and data.
Dashboard, Reports, and Alerts
Dashboard, Reports, and Alerts
All the important information you need is at your fingertips, and everything else is within arm’s reach. Built-in, optimized system dashboards for each role give a 10,000-foot view, with the ability to drill down to any level of detail required for operation, automatically generate reports, and receive alerts.

NetSuite Core Manufacturing

We took the core, scalable NetSuite system and developed an industry-specific IP that allows for a variety of manufacturing solutions, including:

  • Barcoding and warehouse management solutions (WMS)
  • Picking, packing, and shipping
  • Manufacturing WIP
  • Routing and advanced marketing
  • Demand planning

AdaptaLogix also offers quality management, which includes quality specifications and inspections, table data collection, reporting, and integration. Our solutions work in tandem with our CMO supply-chain solutions, so we can be a one-stop shop for all of your manufacturing and distribution needs.

AdaptaLogix Manufacturing Bundle
The AdaptaLogix manufacturing bundle is centered around GxP guidelines and regulations. GxP guidelines were created by the FDA to ensure that pharmaceutical products are safe, meet their intended use, and adhere to quality standards and processes for manufacturing, control, storage, and distribution. The bundle includes:

  • GxP vendor onboarding
  • GxP material onboarding
  • Approved suppliers and materials list
  • GxP purchasing process
  • GxP inventory process
  • GxP manufacturing process
  • GxP final product release
  • Security configuration
  • CFR 21 part 11 compliance
  • Dashboards, reports, and alerts
Manufacturing centered around GxP guidelines

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