Clinical Research
Global Clinical Research is a Biopharmaceutical Service provider and full-service CRO, providing services to pharmaceutical, biotechnology and medical devices companies. We apply our innovative technologies, therapeutic expertise and a commitment to quality to help clients and partners accelerate the delivery of safe and effective therapeutics and maximize the returns on their R&D investments.
Clinical Operation
Our dedicated team has experience in coordinating phase II to IV trials. We can perform all stages of clinical trials-from feasibility to final study report -to the highest quality standards.
We have the therapeutic experience, excellent cooperation with site staff, and in-depth knowledge of local requirements. Our core expertise and focus are in Nepal and other countries through our partner CROs. Our resourcing model provides both the flexibility and local knowledge of each country that the study requires.
The monitor plays a significant role to ensure project success. As a company committed to Clinical Research Excellence, we designed the role of our monitors to go beyond, than simply meeting the technical accuracy demanded by the research.
Our CRAs are trained to predict site management issues and proactively develop and implement solutions. CRAs undergo a thorough instructional regimen and are trained. This approach is employed from the earliest stages and throughout the conduct of the clinical study, to ensure the proper flow and responsiveness of the process.
All our monitors are full-time bilingual employees, equipped with laptops and are always available through mobile phones and the internet when they are off-site.
Whether helping your organization handle an overload of work on a single project or designing a full-service clinical program for your product, Global clinical trials management team has the experience and knowledgeable staff members ready to assist you.
- Clinical services custom-tailored to fit your needs
- Study document development
- CRA management and quality control
- Clinical monitoring and site management
- Clinical Trial Management System
- Investigator meeting planning
- Third-party vendor management
- Audits and preparation for audits
- Training
- Patient recruitment and retention strategies
- Feasibility studies
- Quality training of clinical associates
