Free up your time! I am thoroughly familiar with FDAAA 801, NIH, and ICMJE requirements for registration and results reporting on ClinicalTrials.gov and can assist you with the following:
* Create registration record and obtain NCT# (PI must approve and release record to PRS review.)
* Complete the data entry for results reporting (PI must approve and release record to PRS review.)
* Make required periodic updates to s record
* Upload required documents (protocol and Informed Consent Form) to ClinicalTrials.gov
If you plan to publish, contact me BEFORE you enroll the first participant! Very reasonable rates!
do NOT contact me with unsolicited services or offers