Why VISTA?
VISTA is the only automated solution tailored to meet your site assessment needs
for clinical studies!
Pharmaceutical sponsors’ SOPs mandate site assessment to ensure that the right
sites are selected for a study. However, existing manual assessment methods are
slow and inefficient. Clinical staff end up spending unnecessary weeks trying to
get the information they need from potential sites.
In contrast, VISTA speeds up your site assessment process and is designed
specifically for ease of use by your clinical staff and investigators. VISTA
ensures that all the information you need for site assessment is efficiently captured
and reported from remote sites anywhere in the world, thus helping you achieve
faster and better site selection decisions.
Still not convinced?
Here are some reasons why VISTA is your best choice:
- Quick deployment to meet tight study timelines
- Fast set-up of company or study-specific portal with personalized URL
- Short turnaround time required for VISTA to customize and develop your online site feasibility and qualification questionnaires
- Minimize delays in collecting site information as clinical staff can access data once it is submitted
- Reduced workload for investigators and clinical staff
- User-friendly web format increases convenience for investigators
- Investigators can effortlessly generate automated technical assessment reports without the need for technical expertise
- Automated email/fax reminder system speeds up site responses
- Eliminate double data entry as site data is automatically captured and downloaded directly in Microsoft Excel or other databases
- Cost-effective
- Save valuable time of clinical staff and investigators
- Significantly less expensive than manual site assessment methods
- Security of data collected
- All access is password-protected
- Transmission of data is securely transmitted via a SSL link
- Site data is stored in a fully secure database upon submission
- Strong industry focus
- Proven track record in the areas of clinical trials and pharmaceuticals
- Used successfully in variety of clinical trials by both pharmaceutical sponsors and CROs
- Technology independent
- Easily integrated into your company’s existing systems and processes
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“VISTA is simple and easy for investigative sites to use, and it provides
quick and accurate information for our clinical and support staff. Site assessment
was completed without a hitch and that was my goal when selecting VISTA.”
- Nancy Kohl, President, Quality Data Services, Inc.
“VISTA makes my job so much easier. I don’t have to ask investigators questions
about their PC and connection speed. VISTA automatically gets me all the information
I need.”
– Project Manager, Top 5 CRO
“VISTA made us realize how much information we can collect in future studies
with little time and effort required.”
- Paul Braconnier, President and CEO, Global IQ