Search
Searching Content by Joseph Levitt from Hogan Lovells ordered by Published Date Descending.
Links to Result pages
 
1  
 
Title
Country
Organisation
Author
Date
1
FSMA Implementation: FDA Launches Food Defense Plan Builder 2.0
The Food and Drug Administration (FDA) recently announced the launch of an updated version of the Food Defense Plan Builder Version 2.0 (FDPB)
United States
26 Sep 2019
2
FDA Announces Public Meeting And Docket For Comments On "A New Era Of Smarter Food Safety" To Facilitate FSMA Implementation
The Food and Drug Administration (FDA) recently announced it will hold a full-day public meeting on October 21, 2019, regarding "A New Era of Smarter Food Safety."
United States
25 Sep 2019
3
FDA Issues Updates To Fourth Edition Seafood HACCP Guidance
The U.S. Food and Drug Administration recently released an updated Fourth Edition of its Guidance for Industry entitled, "Fish and Fishery Products Hazards and Control Guidance, Fourth Edition – August 2019".
United States
2 Sep 2019
4
Lawsuit Seeks To Compel FDA To Implement FSMA's Laboratory Accreditation Provisions
Two consumer groups have sued the Food and Drug Administration (FDA) seeking to compel the agency to implement the laboratory accreditation provisions in the FDA Food Safety Modernization Act (FSMA).
United States
28 Aug 2019
5
FDA Issues First Warning Letter for Foreign Supplier Verification Program Violations under FSMA
The U.S. Food and Drug Administration (FDA) recently issued the first Warning Letter addressing violations of the Foreign Supplier Verification Program (FSVP) rule, one of the seven major FDA
United States
23 Aug 2019
6
FDA Announces Reinspection And VQIP Fees For Fiscal Year 2020
The Food and Drug Administration (FDA) recently announced its Fiscal Year (FY) 2020 fee rates, which in particular cover the fees for facility reinspections and participation
United States
31 Jul 2019
7
FDA Finalizes Guidance On How To Determine Whether A Company Meets The "Small Business" Definition Under The FSMA Preventive Controls Regulations
The U.S. Food and Drug Administration (FDA) recently finalized its "Guidance for Industry: Determining the Number of Employees for Purposes of the ‘Small Business' Definition in Parts 117 and 507
United States
26 Jul 2019
8
FDA Issues Draft Guidance On Reducing Microbial Food Safety Hazards In The Production Of Seed For Sprouting
FDA recently released a Draft Guidance for Industry entitled, "Reducing Microbial Food Safety Hazards in the Production of Seed for Sprouting" ("Draft Guidance"). The Draft Guidance
Belgium
15 Jul 2019
9
OMB Releases Spring 2019 Unified Agenda Of Regulatory Actions
This memorandum summarizes the major actions that may be of particular interest to the food industry that are being planned by the U.S. Food and Drug Administration (FDA)
United States
15 Jul 2019
10
FDA Releases Strategy For The Safety Of Imported Food
The U.S. Food and Drug Administration (FDA) recently released the "FDA Strategy for the Safety of Imported Food" (the "Strategy"), which outlines the agency's approach to ensuring the safety
United States
12 Jul 2019
11
Settlement Reached In Lawsuit To Compel FDA To Implement FSMA Traceability Provisions
The U.S. Food and Drug Administration (FDA) reached a settlement with the two consumer groups that sued FDA in October 2018 to compel the agency to implement the traceability provisions in the
United States
5 Jul 2019
12
FDA Encourages "Best If Used By" Labeling To Describe Quality Dates
On May 23, the Food and Drug Administration (FDA) issued a letter to the food industry "strongly support[ing]" the use of "Best If Used By" labeling to describe the date when a food will be at its best flavor and quality.
United States
4 Jul 2019
13
OMB Issues Memorandum Guidance On Executive Departments' And Agencies' Compliance With The Congressional Review Act
The Office of Management and Budget (OMB) recently issued an updated memorandum to the heads of executive departments and agencies entitled, "Guidance on Compliance with the Congressional Review Act" (2019 Memo).
United States
3 Jul 2019
14
FDA Issues Draft Guidance On Initiation Of Voluntary Recalls Under 21 CFR Part 7, Subpart C
The United States Food and Drug Administration (FDA) recently issued Draft Guidance for Industry entitled "Initiation of Voluntary Recalls Under 21 CFR Part 7, Subpart C" (the Draft Guidance).
United States
3 Jul 2019
15
International Dairy Foods Association's Regulatory Roundup Conference
Partner Joseph Levitt and senior associate Veronica Colas presented at the International Dairy Foods Association's Regulatory RoundUP conference on 5 June.
United States
2 Jul 2019
Links to Result pages
 
1