Param Singh

As new non-COVID-related clinical trials proliferate, the need for effective global decentralized CT management is becoming even more apparent. What is needed, says Dr. Harsha Rajasimha of Perficient’s life sciences technology partner Jeeva Informatics, is to expand the capabilities of validated and human-centric digital technology. Clinical trials in certain common serious diseases are on track […]

Life sciences organizations typically manage their IT infrastructure and applications in silos. They implement disparate applications and manage the content and process within those applications separately. They then deploy integrations between those applications to streamline processes and share content and data with different business areas. Much of this work, including the development of integration tools […]

I recently delivered a webinar, in which I discussed the CTMS migration approaches taken across several case studies. You’ll come away with an understanding of: Pros and cons of each CTMS migration method Types of migration tools, including APIs, ETL tools, and adapters Approximate timelines and costs associated with each migration method The topics discussed […]

I recently recorded a video in which I discuss three cost-effective methods to track clinical supplies in Oracle’s clinical trial management system (CTMS): Out-of-the-box clinical supply management (no configuration) Clinical supply management with minimum-level effort configurations Enhanced clinical supply management with medium-level effort configurations This short video shows you just several of the different options […]

Previously, I examined how robotic process automation (RPA) can improve document compliance. The final installment of this series explains how to get started with RPA. The opportunities to use robotic process automation are almost limitless. The examples presented in this guide are just a few areas in which RPA can be used in life sciences […]

Previously, I explained how robotic process automation can assist updating outdated contact details. This blog examines how robotic process automation (RPA) can improve document compliance. Keeping sites in compliance with their required documentation is an ongoing battle for every sponsor and CRO. Considering the volume of documentation involved in a clinical trial, it is no […]

My last blog discussed enhancing slow recruitment with robotic process automation. This installment explains how robotic process automation (RPA) can assist updating outdated contact details. At first glance, having outdated contact information for sites might seem like a relatively minor issue. But when it results in delays related to required documents, monitoring visits, or clinical […]

My last blog dove into robotic process automation fixing mistakes in clinical data entry. This blog highlights enhancing slow recruitment with robotic process automation (RPA). Even the most promising clinical sites can have trouble recruiting enough eligible subjects. Pressure from upper management or the sponsor to meet recruitment targets causes stress and anxiety for study […]

Previously, I discussed life science subject screening and how robotic process automation can assist. This next installment of the series dives into robotic process automation (RPA) fixing mistakes in clinical data entry. Dirty clinical data is one of the most costly aspects of clinical trials. Not only does the review and clean-up slow down time […]

My last blog analyzed site monitoring, and how robotic process automation can enhance it. My next blog discusses life science subject screening and how robotic process automation (RPA) can assist. Even when sites are able to recruit a large pool of potential subjects, sponsors and CROs see far too many subjects who fail to pass […]

Previously I discussed how life sciences companies can establish better relationships with patients. This blog analyses developing a strategic plan and how to get started. When it comes to managing these relationships, the bottom line is that there are some dramatic shifts taking place in healthcare, and life sciences companies need to understand, harness, and […]

Previously, I discussed fixing clinical trial challenges with robotic process automation. This blog analyses site monitoring, and how robotic process automation (RPA) can enhance it. While sponsors, CROs, and sites all acknowledge that site monitoring is a necessary part of ensuring clinical trials are run in compliance with governing regulations and protocols, it can be […]