- I will list your clinical trials on affiliate websites to give maximum exposure for patient recruitment.
- I can also generate disease area specific patient lists of 25,50,75 and 100 just in USA.
- I can also do your clinical trial startup and regulatory paperwork.
- I have 10 years of research experience in regulatory paperwork submissions to the IRB local or central.
- I can cut down your regulatory submission by speeding the submission process so you can get your expedited submission bonus.
- I can help with site feasibility questionnaire so your site is selected each time by the sponsor.
- I can also prescreen patients for your research study.
- I can help fill out your site qualification form as well.
Any research study help you need I can provide asap.