SynMeta is a pioneer technology company that helps businesses to scale-up the quality of service, achieves work efficiency, saves time, reduces costs, TCO (Total Cost of Ownership) and sustains customer loyalty. It's a new generation company that aims to deliver innovative and cost-effective solutions for diverse industry verticals as Financial Services, Telecom, Retail, Insurance, and Healthcare by leveraging the latest technologies – proprietary and open-source, SynMeta aims to provide robust Web Application Development, SAS Development, product consulting and onsite services.
|Headquarters||203 N La Salle St, Chicago IL 60601|
SynMeta’s IT solutions portfolio aims to achieve more with less. Its focus on Mobile & Web application development, Specialized in Open source technologies PHP-CMS, Life Sciences – Biostatistics, Cloud Computing, Payment Gateway Integration, Enterprise application development, Logo & Template Designing, Testing Services, Multimedia and many more with proven expertise in social networks and web analytics, its endeavors are to provide each client complete value from online presence.
Synmeta LLC offers a comprehensive range of medical and pharmacovigilance services essential for the conduct of clinical trials including study preparation, study conduct, medical coding, medical review, and Drug Safety Officer (DSO) activities.
Synmeta LLC offers a comprehensive range of medical and pharmacovigilance services essential for the conduct of clinical trials including study preparation, study conduct, medical coding, medical review and Drug Safety Officer (DSO) activities.
- Safety Database Hosting
Licensed from Oracle, Synmeta LLC has implemented the Argus Safety database and is qualified to use this industry-accepted and proven adverse event management system. This platform enables us to deliver consistent regulatory compliance. Our safety system services cover all aspects of implementation -Technical, functional, regulatory, validation, training and on-going support.Our scientists and in-house trainers help us stay abreast with Oracle Argus safety and its capabilities, in order to maintain quality and compliance
- Medical Writing
Experienced Medical Writing Professionals at Synmeta LLC can design and write a wide range of high quality clinical trial documents in your style / format, efficiently within the prescribed timelines. The department has the experience necessary to deal with the unique challenges of a clinical trial.
- Aggregate Report Writing
At Synmeta LLC, PSURs are written by physicians in consultation with our clients in order to ensure compliance with the applicable regulatory requirements. PSURs are written for mature as well as for life-cycle products.
- Single Case Processing
Following established guidelines, data from source documents sent by clients is processed (data entry and MedDRA coding) in to a Drug Safety/Pharmacovigilance database, after a duplicate search, on behalf of the clients.
- Clinical Data Management
Managing Clinical Data in the existing complex regulatory scenario is the most challenging task. With R&D costs spiraling upwards, patents expiring on many molecules and stringent FDA requirements for new drug approval, it is imperative that there is need to reduce time-to-market and minimize costs.
- Statistical Analysis