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Our Site Management Services provides the Investigator with ongoing support and mentoring as he/she increases their experience for doing clinical research. Our professional staff is available to visit sites as necessary, discuss protocol issues and concerns, review all study documents to ensure that they are correct before submission to the Sponsor, and implement better and more efficient processes that will enable the study staff to work smarter and more efficiently. |
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The PACESETTERS Program is our Investigator training program designed for the novice Investigator and customized for the Investigator with some experience in conducting clinical trials. Even the experienced Investigator agrees that having had formal training prior to conducting any clinical study would have better prepared and equipped him for conducting clinical trials more efficiently. The old school of thought advocating, “on the job training” is no longer sufficient. It is our priority to ensure our Investigators are provided the best training from the start. |
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TAP, our Study Coordinator training program, is designed to equip our coordinators with the knowledge, requisite skills, tools, processes and confidence that set them apart from the conventional coordinator’s style of doing clinical research. Our professionals take pride in their work and are dependable and accessible.
Teachable
Available
Professional
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Our Quality Assurance Services provides peace of mind to our clients in knowing that the Study Monitor as well as the study site are exercising GCPs and performing their duties as outlined by the protocol, FDA and ICH guidelines. We conduct a service review on all of our investigative sites within 30 days of enrollment of the first subject.
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