Our clinical evaluation report consultant team based in Bangalore, India, and serving many leading medical device manufacturers across the Globe. We have all the system, procedures, and human resources to accommodate any clinical evaluation report documentation inquiries for any type of medical device from anywhere in the world.
Clinical Evaluation Website
is a part of I3CGLOBAL!
An award winning regulatory consulting team specializes in medical device and clinical evaluation report consulting domain.
Clinical Evaluation Consulting Process
1. Device Understanding
Every potential Clinical Evaluation Consulting enquiry will be thoroughly studied before answering to potential customers.
2. Quotation and Contract
A detailed proposal with statement of work clearly defining the activities for both manufacturer and consultant. We are open to sign an NDA if required.
3. Advance Payment
As usual in any business, the receipt of advance payment is necessary to open the project. We may take a maximum of 4-5 days to kick off the project.
4. Team Set Up
We set up a team based on the risk class, state of the art, intended use and number accessories/consumables in the device. An average two persons will be deputed per intended use.
5. I3CGlobal team Vs Client team
Team interaction to get required technical information. Good interaction helps the project complete faster.
6. Final Review and Submission
Customer has the choice to select the scope of consulting. (With NB or without NB coordination) On completion of work, the documents submitted to clients.