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ERP Software for Pharmaceutical Manufacturing

Deacom is a comprehensive enterprise resource planning system that enables the process control needed to scale your business

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Maintain all formulation, quality control tests, and documentation in a centralized location.

Enforce strict process control within your production environment.

Provide real-time inventory accuracy with a built-in warehouse management system.

Enable serialization during production.

Adhere to regulations and FDA compliance.

Whether you are a contract manufacturer or produce your own pharmaceuticals, the Deacom ERP platform provides a simplified solution to your complex issues.

21 CFR Part 11 Validation

Validating an ERP system helps pharmaceutical manufacturers ensure that their processes are consistent and operate in accordance with industry standards. Deacom assists with the validation process, establishing documented evidence that, throughout its lifecycle, Deacom ERP will consistently function in accordance with its pre-determined specifications and quality attributes. For pharmaceutical companies validation of the compliance outlined in FDA 21 CFR Part 11 is a critical aspect of the implementation of Deacom ERP.

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Lot Tracking and Traceability

During the production process, Deacom ERP provides the ability to see every lot that went into a production batch. It also provides report details that include who received shipments, their full contact information, lists of all the materials used in a batch, and who specifically performed the transactions. Batch tickets are automatically archived in the system to fulfill FDA requirements during an audit.

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With the capabilities provided by the Deacom AutoFinisher, pharmaceutical manufacturers can have serial numbers automatically generated with their specifications defined in the ERP system itself. It allows you to adhere to the DSCSA rules for serialization of individual units, cases, and pallets by connecting the ERP system and the production equipment responsible.

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With Deacom ERP, manufacturers and distributors are able to leverage Hyper-Tight Process Control™ to help them eliminate the cost of being wrong.

In this brief video, watch a demonstration of exactly how one of Deacom’s native capabilities, the Warehouse Management System, helps to achieve Hyper-Tight Process Control™ by ensuring the right materials are always being picked for production jobs.

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“As our business continues to grow – both by acquisitions and organically – technology will play an important role in upholding our strong market position. With Deacom ERP, we will be able to introduce some of the newest technology advancements throughout our business paving the road for Nexgen’s growth.”

– Mark Nishi, CFO of Nexgen

Nexgen Pharma

Accomplish all of this and more with Deacom ERP


Keep better tabs on your tight margins, tracking all actuals and budgets for expenses, revenue, P&L, and cash flow statements.

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Material Requirements Planning

Use the MRP system to make informed decisions on production needs based on time, inventory levels, and customer demand.

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Formula Management

Provide R&D teams with the tools to develop, maintain, and track formulations, manage workflows, and define quality control checks from raw materials through finished goods.

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Quality Control

Assure product safety with built-in process controls that enforce quality checks at various points in your production.

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Production Weigh Up

Increase the speed and accuracy of the production weigh-up process with built-in controls that provide operators with the exact information they require.

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Document Generation

Automatically generate Certificate of Analysis (COA), product specification, quality control, and other documents as they are required.

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Explore some of the other industries we serve

Contract Manufacturing

Contract Manufacturing

Manage the needs of multiple customers within a single system, generate customer specific documents, and meet production demands with MRP scheduling tools.

Cosmetics & Personal Care

Cosmetics & Personal Care

Maintain formulations, facilitate inter/intra company transfers, and ensure proper labeling requirements are met.



Limit sales to patients based on item attributes such as THC and CBD levels, comply with all regulatory reporting, and track plant life cycles and the cultivation process to improve raw material planning activities.



Enforce quality control checkpoints in your production, maintain strict lot control, and generate customer specific COA documents.