Federal Register

Source: www.fda.gov --- 4 days ago
The FDA is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995. ...

Source: www.fda.gov --- 4 days ago
The FDA is announcing an opportunity for public comment on the proposed collection of certain information by the agency. ...

Source: www.fda.gov --- 4 days ago
The FDA is confirming the effective date of October 15, 2008, for the final rule that appeared in the Federal Register of June 2, 2008 (73 FR 31358). ...

Source: www.fda.gov --- 2 days ago
This notice announces a forthcoming meeting of a public advisory committee of the Food and Drug Administration (FDA). The meeting will be open to the public. Name of Committee: General and Plastic Surgery Devices Panel of the Medical Devices Advisory... ...

Source: www.fda.gov --- 17 days ago
The FDA is is publishing a list of premarket approval applications (PMAs) that have been approved. This list is intended to inform the public of the availability of safety and effectiveness summaries of approved PMAs through the Internet and... ...

Source: www.fda.gov --- 26 days ago
The FDA is confirming the effective date of October 27, 2008, for the final rule that appeared in the Federal Register of June 13, 2008 (73 FR 33692). The direct final rule amends the MDR regulation by removing the requirement for baseline reports. ...

Source: www.fda.gov --- 30 days ago
The draft guidance describes a means by which the absorbable hemostatic device may comply with the requirements of special controls if it is reclassified. FDA is reopening the comment period to update comments and to receive any new information. ...

Source: www.fda.gov --- 19 days ago
The FDA is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995 (the PRA). ...

Source: www.fda.gov --- 24 days ago
This draft guidance document describes FDA's proposed recommendations for clinical investigations of medical devices indicated for the treatment of urinary incontinence. ...

Source: www.fda.gov --- 30 days ago
The FDA is is reopening until October 14, 2008, the comment period for a proposed rule published in the Federal Register to reclassify the absorbable hemostatic device from class III (premarket approval) into class II (special controls). ...

Source: www.fda.gov --- 30 days ago
The FDA is announcing the opening of a public docket to receive information and comments on laser-assisted in situ keratomileusis (LASIK). ...

Source: blog.cleveland.com --- 15 days ago
CLEVELAND -- A U.S. District Judge and the Ohio Supreme Court ruled Monday morning that Ohio voters do not have to wait 30 days after registering before they can cast absentee ballots. Judge James Gwin issued a temporary restraining order... ...

Source: www.idahostatesman.com --- 26 days ago
The U.S. Attorney’s office is making a Federal case out of spilled soda. ...

Source: connect.educause.edu --- 12 days ago
The OCC, Board, FDIC, OTS, NCUA and FTC (the Agencies) are jointly issuing final rules and guidelines implementing section 114 of the Fair and Accurate Credit Transactions Act of 2003 (FACT Act) and final rules implementing section 315 of the FACT Act. The rules implementing section 114 require each financial institution or creditor to develop and implement a written Identity Theft Prevention Program (Program) to detect, prevent, and mitigate identity theft in connection with the opening of certain accounts or certain existing accounts. In addition, the Agencies are issuing guidelines to assist financial institutions and creditors in the formulation and maintenance of a Program that satisfies the requirements of the rules. The rules implementing section 114 also require credit and debit card issuers to assess the validity of notifications of changes of address under certain circumstances. Additionally, the Agencies are issuing joint rules under section 315 that provide guidance regarding reasonable policies and procedures that a user of consumer reports must employ when a consumer reporting agency sends the user a notice of address discrepancy. ...

Source: www.wafb.com --- 14 days ago
The Federal Emergency Management Agency (FEMA) is reaching out to Louisiana landlords to Register their available rental units to help link families displaced by the recent hurricanes with homes. ...

Source: rescommunis.wordpress.com --- 21 days ago
by P.J. Blount with the blog faculty The Department of Defense published a notice on Preservation of Continuity for Semi-Codeless GPS Applications in today’s Federal Register (73 F.R. 54792-54793): SUMMARY: To enable an orderly and systematic transition, the U.S. Government has established December 31, 2020 as the date by which users of semi-codeless/codeless receiving equipment are expected [...] ...

Source: www.extension.iastate.edu --- 27 days ago
DOCID:fr16se08-23 AGENCY: Food Safety and Inspection Service, USDA. ACTION: Notice. SUMMARY: The Food Safety and Inspection Service (FSIS) is announcing that, since January 28, 2008, its laboratories have implemented a revised laboratory methodology for detecting and identifying E. coli O157:H7 in regulatory verification samples. This new method can be found in the Microbiology Laboratory Guidebook (MLG), Chapter 5.04. ...

Source: www.methedemic.com --- 43 days ago
Federal court digest: Dealer wins appeal, but gets more time The longer punishment resulted from the prosecution's decision not to agree to a smaller amount of methamphetamine for which Gonzalez originally was held … Press-Register - al.com - Mobile,AL,USA ...

Source: www.cbc.ca --- 12 days ago
The Federal do-not-call list is back up and running after faltering and crashing for most of the first day Tuesday because of a deluge of people trying to Register. ...