Visual Edge Consulting & Software specializes in information technology project management and process improvement for companies in the pharmaceutical and healthcare industries.

We focus on employing technology and standards in GxP environments to enable efficient business processes and successful technology deployment. Our experience spans the drug development life cycle, including discovery, pre-clinical, clinical, regulatory, and marketing. We work to help our clients realize cost savings and efficiencies in the development of their products and therapies through the application of proper processes, standards, and technology.

Examples of our work include transforming pre-clinical data using the Standard for Exchange of Nonclinical Data (SEND) for FDA submission; enabling the submission of digital ECGs using Clinical Data Interchange Standards Consortium (CDISC) / HL7 standards; implementing clinical safety and clinical drug metabolism laboratory information management systems (LIMS); improving clinical development and pharmacovigilence workflows; performing technology due diligence for a variety of pharmaceutical related software products for various investment companies; developing proposal and systems development processes for major software vendors; and leading the implementation of electronic data capture (EDC) to raise the quality of clinical data and reduce overall clinical trial cost.

Learn more about the work we have done.