ML20044A714
| ML20044A714 | |
| Person / Time | |
|---|---|
| Issue date: | 05/07/1990 |
| From: | Taylor J NRC OFFICE OF THE EXECUTIVE DIRECTOR FOR OPERATIONS (EDO) |
| To: | Thurmond S SENATE |
| Shared Package | |
| ML20044A715 | List: |
| References | |
| FRN-55FR1439, RULE-PR-35 CCS, NUDOCS 9007020124 | |
| Download: ML20044A714 (2) | |
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May 7, 1990 t
1he Fenorable Strom Thurmond United States Senate Washington, DC 20510
Dear Senator Thurmond:
a Thank you for your letter of April 16, 1990'(Case number 0102120025)regat: ding comments by Dr. Mark C. Bruels of Greenville,-South Carolina on proposed amendments to 10 CFR Part 35.
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o The Nuclear Regulatory'Comission published a proposed. rule on' January 16,'1990,.
t on " Medical Use of Byproduct Material" that would require medical use licensees to implement a basic quality assurance program and that would-modify the reporting and recordkeeping. requirements, i The public. coment period closed April 12, 1990. To date, we have received 66 public coment letters, including Dr. Bruels' letter which was enclosed with your letter.
The issues raised by the public comments will be evaluated and used in determining the need for, and if needed, the form of affina11 rule.
In addition, we are conducting a pilot program to try outjthe proposed performance f
based regulatory requirements using a projected 65 Volunteer lrnedical use' licensees from across the United States. Their experience,- evaluations, and suggestions will also be evaluated as aart of cer' activities to determine the-need for a final rule, and if needed tio specific for: p the rule.-
I want to assure you that Dr. Bruels' coments will.be carefully considered with the other public com.nents in our evaluation.
I trust that the above information.is responsive to your request.
Sincerely,
[
J es M. T or
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ecutive irector 4
for Operations i
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a i-May 7, 19901 The Honorable Strom Thurmond l'nited States Senate Washington, DC 20510
Dear Senator Thurmond:
Thank you for your letter cf April 16,1990(Casenumber 0102120025) regarding coments by Dr. Mark C.L Bruels of Greenville, South Carolina on proposed amendments to 10 CFR Pnrt 35.
The Nuclear Regulatory Comission published a proposed rule on January 16, 1990,-
on " Medical Use of Dyproduct Material" that would require medical use licensees to implement a basic quality assurance program and tha+ would modifyithe:
reporting'and recordkeeping requirements. The public ant period closed April 12 1
.oment letters',. including Dr. Bruels'990. To date, we have received 66 publi letter which was enclosed with your letter.
The issues raised by the public coments will be evaluated and:used in determining the need for, and if needed, the form of a final rule..In addition, we are conducting a pilot program to try out the proposed performance based regulatory requirements using a projected 65 volunteer medical;use licensees from across the United States. Their experience, evaluations, and suggestions will also be evaluated as part of our activities to deterinine the-need for a final rule, and if needed the specific form of the rule.
I want to assure you that Dr. Bruels' coments will be carefully considered with the other public coments in eur evaluation.
I trust that the above information is responsive to your request.
Sincerely, Original Signed Bys James M. Taylor James M. Taylor Executive Director for Operations
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