Welcome to Emmes India
In 2006, we opened the doors to our new office in Bangalore, with the passion and commitment to address important health initiatives in India.
This greatly enhanced our ability to serve our clients, not only here in India but in a variety of locations, with high-quality clinical research services supporting Phase I to IV studies. The fact that we’ve worked in more than 40 countries validates the need for a global presence, and our staff members possess a variety of skills and speak multiple languages.
Our highest priority is the integrity of our research. Our scientific collaboration has produced a wide range of studies across diverse disease areas, with patient populations ranging from neonates to elderly. Our proprietary software gives us a great advantage, with more than 20,000 users at over 2,000 sites and laboratories around the world.
We understand what is at stake in your project, and choosing Emmes to support your clinical research will provide you with the expertise and the experience to bring the effort to a scientifically sound conclusion. We are committed to using the highest possible ethical and quality standards.
We provide professional leadership and experience in study design, interim monitoring, selection and execution of statistical analyses, and interpretation and presentation of data. Our statisticians also offer training and instruction to internal and external staff, as well as authoring scientific articles in leading International journals. Study participants’ safety, data quality and site performance are subject to continuous review by this group.
- Analytics and reporting
- Independent Data and Safety Monitoring Board services
- CDISC implementation and data standardization services
Data Management and Site Monitoring
Emmes specializes in providing data management and monitoring support for clinical projects. Our team excels in development and implementation of sophisticated systems and processes used in all phases of organizing, collecting, managing, interpreting and reporting data for projects.
- Collaboration in study design and analytics
- CRF development and database design
- Data management documents preparation
- Data coordination and protocol monitoring (on-site and risk based)
- Data quality review
- Protocol and regulatory compliance
Emmes IT professionals play an essential role in the support of clinical trials. Their goal is to understand the protocol requirements and to customize Advantage eClinical to provide reliable data capture and an informatics platform that supports the collection of high-quality data. Ultimately, this enhances the analysis by Emmes’ statisticians and data managers. System documentation, security, integrity and study participant confidentiality are an integral part of our products.
Advantage eClinical is Emmes’ unified clinical trials platform that was developed by statisticians, medical officers, programmers, data managers and analysts. Our integrated ecosystem of tools allows you to design your clinical trials, ensure timely data collection, manage data quality, and report on critical outcomes. It conforms to 21 CFR Part 11 and other relevant regulatory norms, and it is a CDISC ODM-certified product.
Emmes provides the necessary project leadership to organize staff teams, work in collaboration with sponsors and clinicians, and manage many facets of clinical research in a timely manner. Our experience enables us to reduce the start-up time by relying on our repository of tested solutions across therapeutic areas.
- Collaboration with sponsors, clinicians, participating scientists, and review boards
- Assurance of quality and timeliness of project deliverables
- Oversight of project team and activities
Emmes India is working with a large vaccine manufacturer in India to provide project management, clinical data management and statistical support for one of its studies. The study evaluates the safety and immunogenicity of a newly developed vaccine for seasonal influenza.
Emmes India is providing statistical design and analyses support to evaluate a medical device targeted to improve drug adherence in TB patients and helping prevent multi-drug resistant TB.
Unit #3, The Mayfair, 316, 100 Feet Road,
Indira Nagar, Bangalore, India - 560 038