Emissary International has been navigating the clinical trials process for over a decade, earning itself a second-to-none reputation with clients in the medical device, pharmaceutical, biotechnology and contract research organization (CRO) industries. In the complicated waters of clinical research, successful companies are guided by the foresight and expertise of an experienced partner. Since 1995, Emissary has been leading rigorous, detail-focused clinical research studies across a broad range of therapeutic areas, helping clients bring dozens of new medical products to market quickly and efficiently.
In the complicated waters of clinical research, successful companies are guided by the foresight and expertise of an experienced partner like Emissary International.
By combining Emissary’s therapeutic experience and a suite of technology-enhanced clinical trial services with the project management capabilities of a traditional contract research organization, the company has been able to launch enduring partnerships with a broad array of sponsors — from pharmaceutical and biotechnology companies to medical device manufacturers — and even with other contract research organizations that rely upon Emissary’s experienced monitors and the company’s electronic data capture (EDC) technology to supplement their service offerings.
Time-to-market pressures play a defining role in new medical product development, perhaps now more than ever. In this environment, experience and knowledge become critical in expediting clinical research programs. This is the reason Emissary places high value on the experience of its team. Emissary is proud of its track record in the vigilant planning, managing and monitoring of clinical research studies. This means the soundness of a clinical trial is never in question, and investigational new product development goals are reached without delay. No two clinical trials are alike, which means every Emissary partnership is anchored by the individual needs of the clinical development project at hand.
Emissary supports clients with a broad range of
regulatory-compliant services including:
- Clinical Protocol Development
- Case Report Form Design
- Electronic Data Capture (EDC) System
- Investigator Identification & Qualification
- Monitoring and Project Management
- Clinical Site Management
- Data Management & Statistical Analysis
- Medical Writing & Regulatory Submissions
- Auditing and Quality Assurance
Emissary’s in-depth clinical research experience also led to the development of TeamTrials© Web-based electronic data capture (EDC) platform for streamlining the clinical trials process. In building the TeamTrials platform, Emissary leveraged its expertise in how clinical trials are conducted to ensure that the system delivers efficiency throughout the entire process – from study setup to database lock. TeamTrials is incorporated into day-to-day operations, helping Emissary save time and cut costs for clients’ clinical development projects, and enabling the participants in the clinical trial to work together as a team.
TeamTrials enables easier collaboration among all members of a clinical research team. TeamTrials isn't just an electronic version of a paper-based trial, it is designed to make every step of the clinical trial more efficient, to make every team member's job a little easier. Naturally, TeamTrials supports open standards to enable smooth integration throughout the clinical development process.
Because, Emissary has the team, the experience, and the technology to accelerate your clinical trial and guide your project to success, even over the roughest seas!