Please Wait...

Bioclinica and ArisGlobal Partner to Transform Pharmacovigilance Model

Comprehensive cloud solutions and services lower costs, raise quality

April 18, 2016

Bioclinica®, Inc., a specialty clinical trials technology and services provider, today announced the selection of ArisGlobal's Safety Cloud as the preferred safety platform for its pharmacovigilance services. Under this partnership, Bioclinica becomes the preferred partner for ArisGlobal in business process consulting and change management as sponsors implement or upgrade LifeSphere Safety MultiVigilance. Together the partnership brings a flexible delivery model that fits any organization regardless of size or case volume.

A top 20 pharmaceutical company has already selected Bioclinica to standardize its safety case processing service on the ArisGlobal platform, while two other companies are making the switch from competing platforms. "Early adoption speaks to the strength and value of our joint solution in addressing industry's long-wanted desire for such a safety offering," said Bioclinica President of eHealth Solutions, Mukhtar Ahmed.

ArisGlobal Vice President of Safety George Philips said, "Through our partnership with Bioclinica, we are able to provide the pharmaceutical industry with an unprecedented level of streamlined and cost efficient end-to-end pharmacovigilance services." The cloud-based solution replaces traditional on premise safety systems unpopular with many organizations due to burdensome management, maintenance, and fiscal challenges. "By utilizing these services, resources within an organization can now be shifted to address other pressing needs."

ArisGlobal, and Bioclinica's Safety and Regulatory Solutions division, formulated this comprehensive partner strategy to deliver cost-effective and regulatory compliant services. Bioclinica's Global Consulting group provides organizations with business and change management expertise when implementing or upgrading to new versions of LifeSphere Safety MultiVigilance, including ROI optimization, SOP creation, system validation and development of agile database conventions.

"The formation of this partnership addresses the full continuum of pharmacovigilance as a service," Ahmed remarked. "Together Bioclinica and ArisGlobal provide the most comprehensive solution, whether an organization wants to handle safety internally or outsource it to our team of safety experts."

Looking toward the next wave of innovation, the partners are already working closely to develop ArisGlobal's next generation of products, which combine medical knowledge with innovative technologies derived from such areas as artificial intelligence, machine learning and natural language processing. Bioclinica's president of Safety & Regulatory Solutions Sankesh Abbhi said, "We are creating solutions that remove the struggle involved in assembling the required safety reports, which can be especially difficult in studies where therapies carry intense safety monitoring requirements."

Phillips added, "ArisGlobal currently has an extraordinarily high customer satisfaction rating, and our investment in innovation and automation demonstrates, in return, our commitment to our customers." Bioclinica has joined ArisGlobal's Industry Standard Platform (ISP) forum, providing expert advisory in safety and regulatory to organizations from around the globe.

Find out more about Bioclinica and its eHealth Solutions at www.Bioclinica.com, on the Trial Blazers blog at http://www.bioclinica.com/blog, and on Twitter at http://twitter.com/bioclinica.

About ArisGlobal®

ArisGlobal is a visionary technology company that’s transforming the way today’s most successful life sciences companies develop breakthroughs and bring new products to market. The ArisGlobal LifeSphereTM cognitive technology platform integrates machine-learning capabilities to automate the core functions of the product lifecycle. Designed with deep expertise and a long-term perspective that spans more than 30 years, our cognitive platform delivers actionable insights, boosts efficiency, ensures compliance, and lowers total cost of ownership through multi-tenancy.

Headquartered in the United States, ArisGlobal has regional offices in Europe, India and Japan. For more information, visit arisglobal.com or follow ArisGlobal on LinkedIn and Twitter.

 

About Bioclinica
Bioclinica is a global life sciences solution provider that utilizes science and technology to bring clarity to clinical trials – helping companies to develop new life-improving therapies more efficiently and safely. Successful clinical trials require the ability to see key details and uncover hidden insights, and Bioclinica’s hundreds of experienced scientific, medical, and domain experts bring unmatched insight across the development lifecycle, from the initial protocol to post-approval.  The company’s cloud-based offerings include medical imaging, cardiac safety, randomization and trial supply management and optimization, electronic and eSource data capture, site payments and forecasting, pharmacovigilance, trial management, and risk-based monitoring solutions. A true multifaceted partner to trial sponsors and Contract Research Organizations (CROs), Bioclinica offers an integrated App xChange partner ecosystem, a global network of research sites, patient recruitment services, and post-approval research expertise to provide committed, detail-focused service through all stages of drug development.  The company’s thousands of employees serve more than 400 pharmaceutical, biotechnology and device organizations – including all of the top 20 biopharmaceutical companies and leading CROs – through a network of offices in the U.S., Europe, and Asia. Learn more about Bioclinica at www.Bioclinica.com and on Bioclinica LinkedIn and Twitter.

LEARN MORE OR SPEAK WITH OUR EXPERTS

CONTACT US
Leader in Clinical Trial
Management Solutions

Bioclinica is organized into three business segments so that we can provide expert service and multifaceted technologies. Our Medical Imaging & Biomarkers segment includes an Imaging Core Lab, a Cardiovascular Safety division, and a Molecular Marker Laboratory. Our eHealth segment comprises eClinical Solutions, Randomization & Trial Supply Management, Safety & Regulatory Solutions, and Financial Lifecycle Solutions. Under the Global Clinical Research segment, we offer a network of research sites, patient recruitment, and a Post-Approval Research division.

Great advice on imaging in #clinicaltrials! https://t.co/adsP8h99Ic
bioclinica (2 days ago)
https://t.co/UZQTot9ovJ
bioclinica (2 days ago)
RT @Xtalks: When is Central Imaging Needed in #ClinicalTrials? @bioclinica https://t.co/fYGvqU46TI
bioclinica (2 days ago)
RT @phillytechnews: 11/7: BioClinica, USA Technologies buy California firms ; First Round names female general partner https://t.co/MAvm6…
bioclinica (2 days ago)
RT @eClinical_Jen: Content from the FDA Webinar on Study Data Technical Conformance Guidelines is here: https://t.co/14eepSOR7b #ITTX17
bioclinica (2 days ago)
RT @CenterWatch: .@US_FDA approves first #digital pill with sensor to track #patients adherence, https://t.co/XaEctKIFRx
bioclinica (2 days ago)

Latest Blogs:

Removing Risk from Clinical Trial Management System (CTMS) Implementations
Collaboration Between Clinical Operations and the Logistics and Supply Chain Teams is Key to Trial Success
The Value of Protocol Review
CTMS and RBM: Hot Topics at OCT Nordics in Copenhagen
Congressman Meehan and Bioclinica CEO John Hubbard at recent visit to Bioclinica's Audubon offices