Smart Vision Technologies

SAS makes sense of information by combining its intelligent search, information access and data integration technologies with intuitive visual analytics so our customers can efficiently predict, prevent and respond to threats in real time. Our solutions have a wide and varied application, and our highly tuned solutions for the Public Security market include integrated and modular intelligence management systems and latterly full end-to-end information management systems for the Enterprise. With government agencies and private industry facing similar threats and looking to develop their own in-house intelligence management systems, we have also taken our core intelligence expertise and world-beating search technology into these sectors. SAS has allowed government agencies and private sector organizations to combat their own threats such as sports and financial fraud, rogue trading, malpractice, counterfeiting, piracy and online fraud e.g. phishing, cybersquatting etc.

At Smart Vision Technologies, our clinical data management and consultancy services are dedicated to providing you with clinical data, data analysis, and regulatory support and presentation requirements. The increasing role of a dedicated Clinical Research Organization in your company's clinical data requirements.
At Smart Vision Technologies, our clinical data management and consultancy services are dedicated to providing you your clinical data, data analysis, regulatory support and presentation requirements. Within clinical data management, optimal therapeutic designs, customer support and customized data analysis are key areas where our bio statisticians and medical writers interact to provide comprehensive solutions. Only through an all-inclusive understanding of study objectives, clinical design issues, and upgraded quality control measures, can maintenance of the quality of data and adherence to expected deadlines be achieved. Analysis of clinical trials includes pharmacokinetic and dynamic evaluations, therapeutic equivalence testing and sequential designs.

Faster trial design and planning processes

More efficient collection and management of both patient and trial administration data

Improved FDA compliance

Secure, centralized access to sites, trials, and programs

High accuracy data entry

Comprehensive data validation

Full electronic Audit Trail