Clinical Evaluation 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 CER documentation inquiries for any type of medical device from anywhere in the world.
An award winning regulatory consulting team specializes in medical device domain.
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Why Work with Us
Our global clinical evaluation consultants work without boundaries and will go above and beyond to complete each project on time and to perfection to obtain regulatory approvals. In addition, we provide you with fixed prices and high-quality staff daily till you achieve success!
Medical Device Industry Experience
Highly Qualified Team
Creative & Professional
Payment based on Progress
Clinical Evaluation Report : The process
1. Device Understanding
Every potential Clinical Evaluation Report CER 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.