Request For Proposal - 21 CFR 820 / FDA Inspection

To build a GMP system and implement standard rules, the organization should select an expert team to interact with process owners in your orgnization.

1. MANUFACTURER INFORMATION

Legal Manufacturer Name *:
Street *:
City / Pincode *:
Country *:
Website Address :

2. ADMINISTRATIVE INFORMATION


Scope of I3CGLOBAL :
Scope of Manufacturer :
Number of employees covered in the above scope :
Documentation and Device Knowledge of the person coordinate with Consultants :

3. MEDICAL DEVICE DESCRIPTION

Type of Device:
Name of the Medical device(s) :
Medical Device Class :


4. SUBMITTER INFORMATION

Contact Person * :

4.2 Job Title * :

Contact Number *:

Contact Email *:

Date :