MEDICAL DEVICE GOOD MANUFACTURING PRACTICE REGULATIONS

ICR 198204-0910-004

OMB: 0910-0073

Federal Form Document

Forms and Documents
Document
Name
Status
No forms / supporting documents in this ICR. Check IC Document Collections.
IC Document Collections
IC ID
Document
Title
Status
109569
Migrated
ICR Details
0910-0073 198204-0910-004
Historical Active 198003-0910-001
HHS/FDA
MEDICAL DEVICE GOOD MANUFACTURING PRACTICE REGULATIONS
Revision of a currently approved collection   No
Regular
Approved without change 07/02/1982
Retrieve Notice of Action (NOA) 04/07/1982
  Inventory as of this Action Requested Previously Approved
04/30/1985 04/30/1985 04/30/1982
7,273 0 5,312
80,403 0 1
0 0 0

THE REQUIREMENT OF THE GMP REGULATIONS ARE IN INTEGRAL PART OF AN EFFECTIVE QUALITY ASSURANCE PROGRAM FOR THE MANUFACTURE OF DEVICES, AND AN ESSENTIAL MEANS BY WHICH THE MANUFACTURER ESTABLISHES CONTROL OVER THE MANUFACTURING PROCESS. SUCH CONTROL IS NECESSARY TO ASSURE FINISHED DEVICES CONFORM TO THEIR ESTABLISHED SPECIFICATIONS, AND ARE SAFE AND EFFECTIVE.

None
None


No

1
IC Title Form No. Form Name
MEDICAL DEVICE GOOD MANUFACTURING PRACTICE REGULATIONS

  Total Approved Previously Approved Change Due to New Statute Change Due to Agency Discretion Change Due to Adjustment in Estimate Change Due to Potential Violation of the PRA
Annual Number of Responses 7,273 5,312 0 0 1,961 0
Annual Time Burden (Hours) 80,403 1 0 0 80,402 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
No
No

$0
No
No
Uncollected
Uncollected
Uncollected
Uncollected

  No

On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
 
 
 
 
 
 
 
    (i) Why the information is being collected;
    (ii) Use of information;
    (iii) Burden estimate;
    (iv) Nature of response (voluntary, required for a benefit, or mandatory);
    (v) Nature and extent of confidentiality; and
    (vi) Need to display currently valid OMB control number;
 
 
 
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.
04/07/1982


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