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how it works

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Sargon Research will take care of the regulatory and start-up work to ensure that your site can initiate your trial with ease. Our team will handle all revenue, IRB, and regulatory submissions to save you time and hassle

Before any patients are enrolled, we train all staff members (virtually or in-person) on the specific protocol and study processes. We work closely with your team to develop a tailored training program that covers all aspects of your study protocol. We also help plan study visits and ensure that staff has a proper understanding of drug administration

Once a trial has been initiated, we work closely with your site to develop a method for identifying and screening potential subjects, including advertisement. We understand that this can be a common barrier when it comes to clinical trials, but our team has the expertise to help you overcome it

Once patient enrollment has begun, Sargon Research will review patient charts and assist sites in data collection. Our staff will also facilitate communication between the site and the trial sponsor, including preparation for potential audits, sponsor reviews, and monitoring visits

site expectations

We believe that a successful partnership requires a collaborative effort between our team and yours. We ask that you take your responsibilities seriously in order to get the most out of the Sargon Research Network

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ADEQUATELY AND APPROPRIATELY SCREEN PATIENTS- WITH OUR HELP AND ASSISTANCE- TO ENSURE THAT INCLUSION AND EXCLUSION CRITERIA ARE MET AND VERIFIED

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PROPER DOCUMENTATION, AS REQUIRED BY "GOOD CLINICAL PRACTICE (GCP)' GUIDELINES

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ACCOUNTABILITY FOR REQUIRED PATIENT BLOOD WORK, INCLUDING PHARMACOKINETICS (PK) SAMPLES IF NEEDED

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PROMPT AND EFFECTIVE COMMUNICATION WITH TRIAL SPONSOR AND SARGON STAFF. THIS INCLUDES REGULAR ATTENDANCE AT ALL INVESTIGATOR MEETINGS AND PERIODIC VIRTUAL MEETINGS WITH THE SPONSOR AND SARGON STAFF

We have no minimum time required to be part of the network, you are welcome to join at will and leave at will!

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