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Are you a Director, or a member of a research group that is sometimes overwhelmed by the workload?
Through the years, our experienced staff members have earned a well-deserved reputation for providing companies -- like yours-- with expedient, reliable, and focused support for Phase I and Phase II clinical drug development projects.
CHR, Inc., can provide the following services to help you maintain both your time lines and high quality standards:
- Investigational New Drug ApplicationPreparation
- Complete Protocol Writing Services
- Case Report Form Writing
- Investigator Brochure Writing
- Phase I/II Site Selection, Inspection, and Study Monitoring
- Toxicology Study Site Selection, Management and Monitoring
- Pharmacokinetic Data Analysis and Report Writing
- Clinical Report Writing
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