TEC Identifies What Sets Deacom Apart from Competitors

2017 Deacom TEC Certification

Earlier this year, Deacom released the newest version of the software (Version 15) which moved the system to a .NET framework. According to Technology Evaluation Center (TEC), this shift was a “significant milestone in the evolution of the solution.” “The conversion to a .NET framework was a significant investment over the past five years and …

Artisan Spotlight: Maggie Franks, Data Conversion Specialist

Deacom Artisan - Maggie Franks

We have a pretty incredible team – there, I said it! And each month we showcase the incredible accomplishments of Artisan standouts. This month, we celebrate Maggie Franks, one of our Data Conversion Specialists. In a recent talk with the team, Deacom President and CEO, Jay Deakins recognized how valuable our entire Data Conversion team …

Case Study – California Custom Fruits and Flavors

Deacom Case Study - Food Manufacturing

When it comes to a good ERP experience, it’s all about intuitiveness and flexibility, according to this food manufacturing company. The cost of managing their customized software was outweighing its benefits, so the company took action to invest in a strong future for the company. This is California Custom Fruits and Flavors’ story. THE COMPANY …

SDS and GHS Labeling with DEACOM ERP

For manufacturers and distributors of hazardous materials, DEACOM ERP provides support for the creation and management of Globally Harmonized System (GHS) Labels and Safety Data Sheets (SDSs). Revised in 2012, the Federal regulations provided by the Occupational Safety and Health Administration (OSHA) include a set of guidelines for the communication of information on these hazards. …

Nexgen Pharma Makes Moves to Advance Technology

Nexgen Pharma Technology

Specialty pharmaceutical company, Nexgen Pharma, has been experiencing exponential growth over the past few years but it didn’t take long for them to realize that their ERP wasn’t encouraging their development. A change needed to be made. “As our business continues to grow – both by acquisitions and organically – technology will play an important role in …

What You Need to Know About FDA 21 CFR Part 11 Validation

FDA 21 CFR Part 11 Validation Process

Validating an ERP system helps a company ensure that their processes are consistent and operate in accordance with industry standards. The 21 CFR Part 11 validation process establishes documented evidence that, throughout its lifecycle, the ERP system will consistently function in accordance with its pre-determined specifications and quality attributes. For pharmaceutical and medical device companies, …