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 organization.

Company Name *

Address *

Address Line 1

Address Line 2

City

State / Province / Region

Postal Code

Country

Website / URL

Any other business units should be covered?

Scope of 21 CFR 820

Scope of Consultants

Number of Employees *

Person / Employee to Coordinate with Consultants

Yes
No

Documentation & Device Knowledge of the above Person / Employee *

Clean Room Manufacturing

Yes
No

Sterilization Process Involved in the manufacturing.

Yes
No
Outsourced

Number of Devices involved in the scope of 21 CFR 820

Submitter Name *

Designation / Job Title *

Phone *

Email *