Clinical Technology Advisors, Inc. (CTA), a contract business development and support services organization focused on assisting emerging technology companies with their entry and progression into the clinical trials industry, and SIMpill (Pty), a leader in the area of wireless medication compliance technologies, have entered into a Distribution and Services Agreement allowing CTA to sell the SIMpill wireless pill bottle and associated medication compliance services to the biopharmaceutical industry in North America and Europe.
ACTON, Mass. and CAPE TOWN, South Africa, May 2, 2005 --Clinical Technology Advisors, Inc. (CTA), a contract business development and support services organization focused on assisting emerging technology companies with their entry and progression into the clinical trials industry, and SIMpill (Pty), a leader in the area of wireless medication compliance technologies, have entered into a Distribution and Services Agreement allowing CTA to sell the SIMpill wireless pill bottle and associated medication compliance services to the biopharmaceutical industry in North America and Europe. The focus of this Agreement is to offer the biopharmaceutical industry a device that can track and manage real-time medication compliance during clinical trials.
"There have been some sincere attempts to address the issue of medication compliance in a clinical trial environment, but none have the immediacy of the SIMpill wireless solution," stated Dave Rosa, President and Chief Advisor of CTA. "The ability to have a research subject contacted on their cell phone or similar device if they miss a scheduled medication dose is a powerful enforcement tool to ensure that the subjects stay on track with their medication."
"We are very excited to have the resources that CTA brings to our overall strategy to be the leader in producing the most innovative medication compliance devices to address this crucial issue," added Dr. David Green, President of SIMpill. "In South Africa, we have been successfully using the solution to monitor medication compliance in severe diseases such as HIV infection and tuberculosis. I am confident that the solution will add another level of scientific rigor to the clinical trials process."
The SIMpill medication compliance system consists of a standard pill bottle attached to a device that contains the equivalent of a GSM/GPRS wireless phone. The device is programmed with "time tolerances" based upon the dosing schedule of the drug being tested. The bottle sends an SMS message to a central server once the subject opens the bottle. If this message is not received within the time tolerance programmed into the system, an outgoing message is then sent to the subject's cell phone reminding them to take their medication. If the bottle is still not opened within the secondary time tolerance, then a message (SMS, email, or fax) can be sent to a caregiver or investigational site personnel.
CTA will be exhibiting (Booth T-3) at the upcoming International Society for Pharmaceutical Outcomes Research (ISPOR) 10th Annual Meeting in Washington, DC, on May 16th and 17th. The SIMpill device will be available for hands-on evaluation.
About Clinical Technology Advisors, Inc (CTA):
CTA (www.clintechadvisors.com) employs a unique model of providing emerging technology companies with contract business development staff as they introduce or enhance their products and services within the clinical trials industry. CTA also provides study set-up, data management, and field support services to assist pharmaceutical, biotechnology, medical device, and nutraceutical companies with the utilization of technology solutions to expedite data collection during their clinical trials.
About SIMpill (Pty):
SIMpill (www.simpill.com) is a leader in providing innovative, proven, affordable and usable solutions to enable health organizations to be more efficient and effective. Our primary focus is the use of wireless technologies to support patients with chronic conditions to take their medication as prescribed.
Unifying Industry to Better Understand GCP Guidance
May 7th 2025In this episode of the Applied Clinical Trials Podcast, David Nickerson, head of clinical quality management at EMD Serono; and Arlene Lee, director of product management, data quality & risk management solutions at Medidata, discuss the newest ICH E6(R3) GCP guidelines as well as how TransCelerate and ACRO have partnered to help stakeholders better acclimate to these guidelines.
Beyond the Molecule: How Human-Centered Design Unlocks AI's Promise in Pharma
June 23rd 2025How human-centered AI that is focused on customer, user, and employee experience can drive real transformation in clinical trials and beyond by aligning intelligent technologies with the people who use them.
2025 DIA Annual Meeting: Why AI and Automation Are Set to Become the New Normal in Clinical Research
June 20th 2025Peter Ronco, CEO, Emmes, shares his long-term vision for artificial intelligence in clinical research, from making automation routine to improving drug discovery, transforming regulatory oversight, reducing animal testing, and promoting ethical, equitable data use worldwide.