Mindprint Inc. and ethica Clinical Research Inc. announced the successful implementation of a highly effective Enterprise Resource Planning (ERP) system for managing all pre-sales, operations, and finance related processes for ethica Clinical Research Inc. ethica Clinical Research Inc. is a full-service Contract Research Organization (CRO) operating in Canada, Mexico and India that conducts and manages ethical clinical research on drugs, biologics, medical devices, and natural health products. ethica had evaluated multiple ERP systems and found that none fully met their requirements. All of the standard ERP systems either did not have the functionality needed to meet ethica's requirements or were so rigid that ethica would have had to change their internal processes to suit the software.
ethica originally engaged Mindprint for a two-week requirement gathering session that began with an assessment and exploration of ethica's internal work processes and resulted in the generation of the ideal processes for an ERP system that would fit ethica's size and culture. Mindprint then provided a fixed price quote for mapping all of ethica's work processes including customer relationship management, human resources, operations, timesheets, and invoicing into an Axpert based ERP system.
The entire ERP system implementation within ethica's organization (including design, development, installation, and data migration) was done in less than four months. Mindprint's iterative approach ensured that the key users at ethica were highly engaged during the entire implementation process and this resulted in a system that fit ethica like a glove. Mindprint's fixed price approach also significantly mitigated the financial risk of the project for ethica's senior management.
"Mindprint worked very efficiently and intuitively. It was very adept at understanding the complexities of our business processes and simplifying them in the context of developing an ERP system that suited our needs," said Dr. Janice Parente, President of ethica Clinical Research Inc. "Axpert has been successful at consolidating and centralizing ethica's key processes in a way that allows us to manage the business more effectively and efficiently."
Driving Diversity with the Integrated Research Model
October 16th 2024Ashley Moultrie, CCRP, senior director, DEI & community engagement, Javara discusses current trends and challenges with achieving greater diversity in clinical trials, how integrated research organizations are bringing care directly to patients, and more.
AI in Clinical Trials: A Long, But Promising Road Ahead
May 29th 2024Stephen Pyke, chief clinical data and digital officer, Parexel, discusses how AI can be used in clinical trials to streamline operational processes, the importance of collaboration and data sharing in advancing the use of technology, and more.
Carvykti Significantly Boosts Survival, MRD Negativity in Relapsed Multiple Myeloma
December 10th 2024Phase III CARTITUDE-4 trial shows Carvykti significantly improves minimal residual disease negativity rates, progression-free survival, and overall survival compared to standard therapies for patients with relapsed or refractory multiple myeloma, especially when used earlier in treatment.