Existing Research Sites

Contact Newton Clinical Research for more details

NCR provides trial management, site support, training, regulatory submissions, and helps secure new trials for qualified physicians.

Help in site feasibilities

Full Coordinator support for the duration of the study

Training at reasonable cost

ICH/GCP trainings for Coordinators and Principal Investigators

Source document preparations/ Contract and budget negotiations

Help in Sponsor/FDA Audits

Regulatory document preparations and submissions on your behalf

We help you getting new trials to your site for your qualified physicians

Offer back up coordinator services for your primary coordinators

IRB submission

Regulatory Document submissions

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