BROKERS ASSOCIATION SEMINAR SPECIAL PRODUCT REQUIREMENTS

Slides:



Advertisements
Similar presentations
Regulatory Pathway for Platform Technologies
Advertisements

Entering the US Market: Medical Devices
Overview of FDA Device Regulations
"Determining the Regulatory Pathway to Market" Classification Heather S. Rosecrans Director, 510(k) Staff Office of Device Evaluation Center for Devices.
510k Submission Overview Myraqa, Inc. August 22, 2012.
Single Use Expanded Access IND/IDE: FDA and IRB Requirements Before and After Use IRB Webinar October 9,2014.
Clinical Trials — A Closer Look. The Food and Drug Administration (FDA) is the main consumer watchdog for numerous products: Drugs and biologics (prescription.
Processed Food Industry Expanding Exports to the United States Carl C Reynolds.
Medical Device Submissions
FEDERAL REGULATIONS OF MEDICATIONS Food, Drug and Cosmetic Act Protect consumers from adulterated and misbranded foods, drugs, cosmetics, or devices.
Medical Devices Approval Process
U.S. CUSTOMS & BORDER PROTECTION, FDA AND DEPT. OF COMMERCE CENSUS UPDATE WMTA NOV. 19, 2011.
Requirements for Premarket Submissions: In vitro Diagnostic Instrumentation and Software Related to Donor Screening and HIV Diagnostic Assay Systems Diane.
The FDA Landscape AdvaMed September 2008 Judith K. Meritz
Investigational New Drug Application 21 CFR Part 312 A Review for OCRA US RAC Study Group September 2005 Ginger Clasby, MS Promedica International
+ Medical Devices Approval Process. + Objectives Define a medical device Be familiar with the classification system for medical devices Understand the.
Weaving regulations into sound value analysis processes Barbara Strain, MA, SM(ASCP) Director Value Management University of Virginia Health System.
1 The FDA and Animal Drug Compounding Neal Bataller, DVM FDA/Center for Veterinary Medicine AAVPT 14 th Biennial Symposium, May 16-17, 2005, Rockville,
1 1 PDUFA & FDA Legislation FDA Regulatory & Compliance Symposium August 2006 Marc Wilenzick, Moderator for Panel: Dan Carpenter, Harvard Dept. of Government.
FDA Resources and Meetings FDA/EMA Orphan Designation and Grant Workshop Silver Spring, Maryland FDA Campus (White Oak) October 12, 2012 Bill Sutton Deputy.
Dietary Supplements Bradford W. Williams Special Assistant Division of Dietary Supplement Programs ONPLDS, CFSAN, FDA.
Special Issues in FDA-Regulated Studies: The Good, the Bad, and the Ugly C. Karen Jeans, MSN, CCRN, CIP COACH Program Analyst VA Office of Research & Development.
USFDA Canned Food Regulations Thermal Processing Deviations Registration and Process Filing William W. Deckert Jr.
Prof. Moustafa M. Mohamed Vice dean Faculty of Allied Medical Science Pharos University in Alexandria Development and Regulation of Medical Products (MEDR-101)
Carolyn Hommel Good Clinical Practice Program FDA February 25, 2004
Clinical Trials — A Closer Look. The Food and Drug Administration (FDA) is the main consumer watchdog for numerous products: Drugs and biologics (prescription.
1 Importation of Medical Devices FDA Chicago District O’Hare Import Resident Post August 26, 2010 Import Entry Review Team Tamara M. Qtami, CSO.
20__ Fredrikson & Byron P.A A Practical Path -- Does the First Amendment Matter? Presented by Bob Klepinski
REGULATORY CHALLENGES FOR NANOMATERIALS IN PUBLIC HEALTH Driving Faster Than Our Nano-Headlights AAAS Annual Meeting February 13, 2009 Norris E. Alderson,
Abuse Liability and Drug Scheduling: The Role of the FDA Deborah B
When do I need an IND ? FDA Guidance for Industry – Investigation New Drug Applications (INDs) - Determining Whether Human Research Studies Can Be Conducted.
Human Research Protection Program 101 March 19-20, 2007 Cincinnati, Ohio.
Center for Food Safety and Applied Nutrition (CFSAN) Golriz Khadem And Ryan Leitz.
FDA Focus On Consumer Protection
UNCLASSIFIED10/12/ :41 AM Slide 1 Division of Regulated Activities and Compliance.
Columbus Importers and Brokers Association Import For Export April 20, 2011 Presentation by: Robert Rodriguez, IPM, SCSO FDA Cincinnati District
Impact of FSMA on the Regulation of Domestic and Imported Animal Food by Daniel G. McChesney, Ph.D. at Wild Bird Feeding Industry 2011 Annual Meeting Naples,
Latham & Watkins operates as a limited liability partnership worldwide with affiliated limited liability partnerships conducting the practice in the United.
The Regulation of Colors
Humanitarian Use Devices September 23, 2011 Theodore Stevens, MS, RAC Office of Cellular, Tissue and Gene Therapies Center for Biologics Evaluation and.
1 Combination Products: Jurisdictional Issues MassMEDIC Presentation March 28, 2006 Janice Hogan, Esq. Partner Hogan & Hartson, LLP
Overview of FDA's Regulatory Framework for PET Drugs
11/15/20151 Who We Are: Arunava (Ron) Sanyal, M.Pharm,CQE, RAC CEO/President
The FDA Regulatory and Compliance Symposium Preparing for the FDA’s Risk-Based Inspections Presented By: Martin Browning, EduQuest, Inc.
Welcome New IRB Members! Today we will discuss: Your Role in the IRB: What to Know The IRB Review Process Resources Human Research Protections.
Low Acid Canned Foods Dennis M. Dignan, Ph.D. Center for Food Safety and Applied Nutrition November 7, 2003 U.S. Food and Drug Administration College Park,
Affirmation of Compliance (A of C) and FSMA Update Presented by Cornelia Rooks Registrar Corp AIFBA November 2015.
Utah Life Science Summit Nov Phil Triolo, PhD RAC President, Phil Triolo and Associates LC.
HUD and Emergent Use Walter Kraft. Device Classification Significant risk – Often involve an invasive procedure for implantation or use – Requires IDE.
Human Specimen Repositories Requirements of 21 CFR Parts 50 & 56 PRIM & R May 5, 2004 Sally A. Hojvat, Ph.D. Director of Microbiology Devices Office of.
Drug Development and IND Process GC 690 Walter Kraft, MD.
COPYRIGHT ALL RIGHTS RESERVED. LEGAL DISCLOSURE. November 25, 2002 PRESENTATION TO: Public Hearing: FDA Regulation of Combination Products November.
INTRODUCTION Medical Devices ©2014 Salt Lake Community College. All rights reserved.
Device Updates in FDASIA MDUFA III RA SAIC – 9 th April 2013 Karen Jaffe, MS, MBA, RAC or
Get Complete File From exam-dumps.html exam-dumps.html.
A Joint Collaboration Between FDA and AIFBA
Executive Director, Registrar Corp
Essentials of FDA Data Element Submissions
The Seafood HACCP Regulation
Premarket Notification 510(k) process
How to Put Together an IDE Application
Clinical Trials — A Closer Look
Chapter 3 POTENTIAL FOOD SAFETY HAZARDS and CONTROLS
HACCP Guidance for Canned Tuna
Clinical Investigations
FDA Medical Device Approval Pathways
Chapter 2 REGULATORY REQUIREMENTS
FDA Resources and Meetings
Linda M. Chatwin, Esq. RAC Business Manager, UL LLC
The interrelation of good practices: from development to distribution
Presentation transcript:

BROKERS ASSOCIATION SEMINAR SPECIAL PRODUCT REQUIREMENTS January 22, 2009 Chicago District/FDA

Ryan Gibson, Investigator Human Drugs Animal Drugs Medical Devices Medical Devices That Emit Radiation Non-Medical Devices That Emit Radiation Devices: Sunglasses/Reading Glasses Regulations Biological Products Biological Numbers

Human Drugs DLS – Drug Listing Number from the Foreign Manufacturer NDA – New Drug Application from the U.S. Firm IND –Investigation New Drug ANDA – Abbreviated New Drug Application http://www.fda.gov/

ANIMAL DRUGS NAD – New Animal Drug Application Number – Number issued by FDA/CVM to a U.S. Firm/Sponsor ANA – Abbreviated New Animal Drug DLS – Drug Listing Number from the Foreign Manufacturer INA – Investigational New Animal Drug http://www.fda.gov/

MEDICAL DEVICES DEV – Registration number for Importer LST – Medical Device Listing Number PMN – Premarket Notification (510(k)#) PMA – Premarket Approval (“P”#) IDE - Investigational Device Exemption http://www.fda.gov/

Medical Devices That Emit Radiation DEV – Registration Number For Importer LST – Medical Device Listing Number PMN – 510 (k) Number ACC – Accession number 2877 Form – 4 parts to the form A, B, C, D

Non-Medical Devices That Emit Radiation ACC – Accession number from manufacturer 2877 Form – RAA, RAB , RAC, RAD MDL – Model Number

Devices Sunglasses or Reading Glasses DEV – Registration number for Importer LST – Medical Device Listing Number IRC – Impact Resistance Lens Certificate

Regulations (CFR) Use this code plus the qualifier to inform FDA that a product is exempted. Most of FDA’s regulations are in Title 21.

Biological Products BFL – Biological Establishment License Number BPL-Biologic Product Number Biological License Number can be provided using either AofC

Biologic Numbers Biologic 510(k) BK960002 Biologic PMA BP000028 Use Device AofC PMN Biologic PMA BP000028 Use Device AofC PMA NDA BN 040083 Use Drug AofC NDA

Susan Ciani, Investigator Cosmetics LACF/AF: Low Acid Canned Foods and Acidified Foods IFE: Import For Export

Cosmetics If it is a drug, it requires foreign DLS. Concerns about Permitted colors BSE Microbiological content

LOW ACID/ACIDIFIED FOODS FCE – Food Canning Establishment Number Container Dimensions for jars, cans and pouches. SID – Schedule Identifier Number

LOW ACID/ACIDIFIED FOODS PRODUCT CODING CONSIDERATIONS Subclass is important to identifying products subject to LACF Regulations Products that are not hermetically sealed are exempt from LACF Regulations Subclass E (Metal), C (Glass), V (Vacuum or Modified Atmosphere Packgaing)

LOW ACID/ACIDIFIED FOODS PRODUCT CODING CONSIDERATIONS PIC is important to determining which products are subject to LACF Regulations PIC E Commercially Sterile: Product is packed in hermetically sealed container and heat treated to achieve commercial sterility PIC I Acidified: Low Acid Foods that are hermetically sealed to which acid is added

LOW ACID/ACIDIFIED FOODS PRODUCT CODING CONSIDERATIONS Examples Canned Tuna/Commercially Sterile 16AEE45/ Fish/ Metal / Commercially Sterile / Tuna (Albacore, Yellowfin, Bluefin, Skipjack, Etc.) Canned Artichokes/Acidified 24TEI01 Leaf / Stem Veg/ Metal / Acidified / Artichoke (Leaf & Stem Vegetable)

Import for Export Product will be imported into the U.S. but will be exported. Does not require a qualifier. Allows for importation of violative articles.