Conducting new product development and providing testing services in clinical research is the most sensitive and complex procedure demanding highly committed and dedicated research scientists who work in close coordination with clients.
Voxtur has internal control in each and every personal who participated in the execution of the project and nurturing them to meet organizational and regulatory ethical norms and intelligent product and service orientation for timely submission to authorities especially New Drug Application (NDA) and Abbreviated New Drug Application (ANDA), they are,
- As a full-service provider, we offer a complete solution for trials of nearly any size, location, type or phase. Our experienced team has years of knowledge in the unique aspects of the most difficult of projects.
- Our Clinical Operations staffs are knowledgeable about the most advanced principles in Clinical Trial Study Design, and Study Conduct. They also have experience in the most novel treatment modalities that target a broad-range of medical conditions and disease states presented by the current pharmaceutical and biotechnology industries.
- We offer highly-qualified professionals for each service.
- Voxtur manages all facets of the Clinical Study.
- Key focus areas include efficient study start-up; strategic patient recruitment; high-quality yet efficient trial operations; proper trial operations decision making and documentation; and strong clinical research associate (CRA) leadership and oversight.
- Clinical trials are integral part of Drug Development. Voxtur offers end-to-end services for Phase II to IV clinical trials on small molecules, large molecules and medical devices with fully ICH GCP compliant operations.
- Voxtur’s integrated approach to Clinical Trials ensures that sponsors benefit from the entire spectrum of services.