ComplianceOnline

“This education activity has been submitted to the Compliance Certification Board (CCB)® and is currently pending their review for approval of CCB CEUs.”

The U.S. Food and Drug Administration’s Center for Veterinary Medicine (CVM) is responsible for the approval of veterinary drug products intended for both family pets and food-producing animals. However, FDA does not regulate all products intended for animal use. Jurisdiction over animal products including licensed biologics such as vaccines is shared with a number of other federal agencies. For example, animal vaccines, animal disease diagnostic devices and some animal biologics are regulated by the U.S. Department of Agriculture’s Animal and Plant Health Inspection Service or APHIS; and products such as flea and tick collars are regulated by the Environmental Protection Agency.

This seminar on veterinary medicine regulations will provide attendees with an understanding of FDA’s veterinary drug approval process. This two day interactive course will cover:

  • Premarket approval process
  • Various sections of a New Animal Drug Application
  • Strategies for navigating the FDA approval process
Seminar Fee Includes:
Lunch
AM-PM Tea/Coffee
Seminar Material
USB with seminar presentation
Hard copy of presentation
Attendance Certificate
$100 Gift Cert for next seminar

Learning Objectives:

Upon completing this course on veterinary medicine regulations participants will:

  • Understand how the U.S. Food and Drug Administration regulates veterinary drug product.
  • Understand how FDA’s Center for Veterinary Medicine is organized.
  • Discuss the process by which veterinary drug products are reviewed and approved.
  • Learn how to open an INAD File and request fee waivers.
  • Obtain a working knowledge of various sections included within an NADA.
  • Develop a deep understanding of what is needed to substantiate product characterization, target safety and effectiveness.
  • Gain general understanding of FDA’s rules governing chemistry, manufacturing and controls (CMC).
  • Understand the various components of an animal field study to support product approval.
  • Discuss the difference between FDA’s various user fees and fee waivers.
  • Identify the elements of an FDA compliant label.
  • Develop a corporate compliance strategy covering labeling, marketing and advertising.
  • Explore problem solving methods to mitigate regulatory enforcement risks.
  • Explain how jurisdiction is split between various Federal agencies in a certain cases.
  • Learn how animal feed, veterinary devices, OTC drug products and nutritional supplement are regulated in the U.S.

Who will Benefit:

This course is designed for people tasked with developing and maintaining an animal health company’s product portfolio and responsible for overseeing a company’s regulatory strategies. This includes individuals responsible for overseeing regulatory affairs, developing veterinary drug products, evaluating new technologies or applications, and those tasked with ensuring corporate compliance. Among others, this includes:

  • Personnel new to the Animal Health Industry
  • CRO professionals
  • Entrepreneurs looking to add value to their products
  • Regulatory professionals
  • Compliance professionals
  • U.S. Agents of Foreign Corporations
  • Document control specialists
  • Record retention specialists
  • Legal Professionals
  • Financial Advisors and Institutional Investors
  • Consultants, Inspectors and cGxP Experts
Register by phone or need assistance? Call +1-888-717-2436 Register Now Download Brochure
Day 01(8:30 AM - 4:30 PM)
  • 08.30 AM - 09.00 AM: Registration
  • 09.00 AM: Session Start
  • Introduction to Veterinary Drug Approval process
    • FDA’s jurisdiction and Centers relevant to Animal Health
      • Center for Food Safety and Applied Nutrition (CFSAN)
      • Center for Drug Evaluation and Research (CDER)
      • Center for Biologics Evaluation and Research (CBER)
      • Center for Veterinary Medicine (CVM)
    • Specifics of CVM
    • Intro to the FD&CA, AMDUCA, ADAA, FDAMA, MUMS, and guidance documents(GFI)
      • Overview of FDCA and regulations
      • Drugs versus Biologics
      •  Introduction to FDA Guidance for Industry (GFI) and other online resources
  • Overview of Veterinary Drug Development (NADA Pioneer Drugs)
    • Discovery/Acquisition
      • Preliminary Patent Protection Concerns
    • Submissions
      • Open INAD File
        • Sponsor information
        • Responsible Official
        • Product description
        • Target species and proposed indication
      • Early Information
      • Phased review
      • NADA (8 sections)
        • 5 Major Technical Sections
          • Chemistry, Manufacturing and Controls (CMC)
          • Safety (target animal safety study)
          • Effectiveness (clinical field study)
          • Human Food Safety (human food safety studies for food-producing animals)
          • Environmental Impact (EA/CE)
      • 3 Minor Technical Sections
        • Label
        • Freedom of Information summary (FOI)
        • All Other Information (AOI)
      • Administrative NADA
    • Brief Description of cGxP (GMP, GLP, & GCP)
  • Approval Process: Chemistry, Manufacturing Controls, Environmental Impact & Managing Clinical Trials
    • CMC
      • API: name, structure, properties
      • API manufacturing
      • Clinical Trial material
      • Final Formulation
      • VMF/DMF
    • Target Animal Safety
      • Content and format
      • Final Study Reports
      • Monitoring and Reporting Adverse Drug Events
    • Human Food Safety
      • Analysis of Drug Residues
      • Toxicology
      • Residue Chemistry
      • Microbial Food Safety
      • Regulatory Method Relied Upon by Sponsor
    • Effectiveness
      • Dosage Characterization
      • Substantial evidence (e.g. dose confirmation and clinical field studies)
      • All other information related to effectiveness
      • Proposed effectiveness-related labeling
      • Effectiveness Guidance Documents
      • Laboratory studies can be used to provide effectiveness data
      • The 7 Major Phases of Animal Field Studies
        • Planning
        • Study Initiation
        • In-life Activities
        • Site close-out
        • Data management
        • Biostatistical analysis
        • Report writing and preparing raw data files
      • Data collection and study documentation
    • Environmental Impact
      • Categorical Exclusions
      • Environmental Assessments (EA)
      • Common EA Components
      • Environmental Impact Statements (EIS)
    • Labeling 21 CFR requirements
    • FOI
    • AOI
Day 02(8:30 AM - 4:30 PM)
  • Overview of Generic Animal Drugs (JINAD)
    • Submissions
      • ANADA sections
        • CMC
        • Bioequivalence (Safety & Efficacy)
        • Human Food Safety
        • All others
  • Minor Use Minor Species (MUMS)
    • Designation
    • Indexing
  • Animal Drug User Fees and Related Fee Waivers
    • Veterinary Drug User Fees and Fee Reductions and Waivers
    • Animal Drug User Fee Act (ADUFA) – Applies to Innovators Only
    • Animal Generic Drug User Fee Act (AGDUFA) – Applies to Generic Manufacturers
    • Types of User Fees
      • Animal Drug Application and Supplement Fee
      • Animal Drug Product Fee
      • Animal Drug Establishment Fee
      • Animal Drug Sponsor Fee
    • Types of Fee Waivers and Reductions
    • Procedures, Timing and FDA Evaluation of Waivers or Reductions
  • Introduction to FDA’s Regulation of Veterinary Feed, OTC Drugs, Supplements and Medical Devices
    • Animal Feed
      • GRAS – 21 CFR 582
      • Feed Labeling
      • AAFCO
      • Veterinary Feed Directive (VFD)
    • Veterinary OTC Drugs and Nutritional Supplements
      • Regulatory Agencies
      • CVM Compliance Policy - CPG 690.150 & CPG 690.100
    • Veterinary Medical Devices CPG 655.100
  • USDA (CVB, APHIS, FSIS) & EPA
    • USDA’s Animal and Plant Health Inspection Service
      • Virus Serum Toxin Act
        • Animal vaccines
        • Animal biologics
        • Animal disease diagnostic devices
    • EPA
      • Flea & Tick Products
      • Insect Repellants such as Equine Fly Sprays
      • State Registrations
  • Non-Approval-Related Considerations
    • Extra-Label Drug Use
    • Compounding
    • Noncompliance and Enforcement
      • FDA Enforcement Authority over Development, Manufacture, Marketing, and Distribution
        • FDA’s Office of Regulatory Affairs (ORA): Responsible for field activities, imports, inspections, and enforcement policy
        • Local, State, and Tribal governments
        • CVM’s Office of Surveillance and Compliance
      • Types of Enforcement Actions
    • Pharmacovigilance
    • Post-approval submissions
      • CMC
      • Safety
      • Efficacy
Register by phone or need assistance? Call +1-888-717-2436 Register Now Download Brochure
Mark A Hughes

Mark Hughes
Consultant, Hughes Veterinary Consulting

Dr. Mark Hughes, DVM, MS, has over 11 years of experience in veterinary drug product development and over 20 years of experience in laboratory animal medicine, development of in-vitro diagnostic tests, and research in animal reproduction. He has managed or contributed to clinical studies and regulatory submissions on the safety and effectiveness of veterinary drugs (including stem cells) for therapeutic treatments related to dermatology, cardiology, endocrinology, oncology, osteoarthritis, and infectious diseases. Through his consulting business, Hughes Veterinary Consulting, he assists domestic and international biotech and pharmaceutical companies with the process of applying for regulatory approval of drug products for use in companion animals and livestock.

Register by phone or need assistance? Call +1-888-717-2436 Register Now Download Brochure

Register Now

Online using Credit card

$1,899.00

Seminar One Registration

September 26-27, 2019, Kansas City, MO




Your registration fee includes the workshop, all course materials and lunch.


For discounts on multiple registrations, contact customer care at +1-888-717-2436.

Other Registration Option

By order form / PO#

Payment Mode

By Check -
Pay your check to (payee name) “MetricStream Inc” our parent company and Mail the check to:

ComplianceOnline (MetricStream, Inc),
2479 E. Bayshore Road Suite 260
Palo Alto, CA 94303
USA

By Wire -

Register / Pay by Wire Transfer

Please contact us at +1-888-717-2436 to get details of wire transfer option.

Terms & Conditions to Register for the Seminar/Conference/Event

Your registration for the seminar is subject to following terms and conditions. If you need any clarification before registering for this seminar please call us @ +1-888-717-2436 or email us @ customercare@complianceonline.com

Payment:
Payment is required 2 days before the date of the conference. We accept American Express, Visa and MasterCard. Make checks payable to MetricStream Inc. (our parent company).

Cancellations and substitutions:
Written cancellations through fax or email (from the person who has registered for this conference) received at least 10 calendar days prior to the start date of the event will receive a refund - less a $300 administration fee. No cancellations will be accepted - nor refunds issued - within 10 calendar days before the start date of the event.

On request by email or fax (before the seminar) a credit for the amount paid minus administration fees ($300) will be transferred to any future ComplianceOnline event and a credit note will be issued.

Substitutions may be made at any time. No-shows will be charged the full amount.

We discourage onsite registrations, however if you wish to register onsite, payment to happen through credit card immediately or check to be submitted onsite. Conference material will be given on the spot if it is available after distributing to other attendees. In case it is not available, we will send the material after the conference is over.

In the event ComplianceOnline cancels the seminar, ComplianceOnline is not responsible for any airfare, hotel, other costs or losses incurred by registrants. Some topics and speakers may be subject to change without notice.

Attendance confirmation and documents to carry to the seminar venue:
After we receive the payment from the registered attendee, an electronic event pass will be sent to the email address associated with the registrant 5 working days before the seminar date. Please bring the pass to the venue of the event.

Conference photograph / video:
By registering and attending ComplianceOnline conference, you agree to have your photographs or videos taken at the conference venue and you do not have any objections to ComplianceOnline using these photos and videos for marketing, archiving or any other conference related activities. You agree to release ComplianceOnline from any kind of claims arising out of copyright or privacy violations.

Offers:

  • Early bird seats are limited and based on first-come, first-serve.
  • Multiple offers cannot be combined.
  • Online using Credit card

    $1,699.00

    Seminar One Registration

    December 5-6, 2019, Chicago, IL
    (Registrations till September 30, 2019 - $1699)
    (Registrations after September 30, 2019 - $1899)




    Your registration fee includes the workshop, all course materials and lunch.


    For discounts on multiple registrations, contact customer care at +1-888-717-2436.

    Other Registration Option

    By order form / PO#

    Payment Mode

    By Check -
    Pay your check to (payee name) “MetricStream Inc” our parent company and Mail the check to:

    ComplianceOnline (MetricStream, Inc),
    2479 E. Bayshore Road Suite 260
    Palo Alto, CA 94303
    USA

    By Wire -

    Register / Pay by Wire Transfer

    Please contact us at +1-888-717-2436 to get details of wire transfer option.

    Terms & Conditions to Register for the Seminar/Conference/Event

    Your registration for the seminar is subject to following terms and conditions. If you need any clarification before registering for this seminar please call us @ +1-888-717-2436 or email us @ customercare@complianceonline.com

    Payment:
    Payment is required 2 days before the date of the conference. We accept American Express, Visa and MasterCard. Make checks payable to MetricStream Inc. (our parent company).

    Cancellations and substitutions:
    Written cancellations through fax or email (from the person who has registered for this conference) received at least 10 calendar days prior to the start date of the event will receive a refund - less a $300 administration fee. No cancellations will be accepted - nor refunds issued - within 10 calendar days before the start date of the event.

    On request by email or fax (before the seminar) a credit for the amount paid minus administration fees ($300) will be transferred to any future ComplianceOnline event and a credit note will be issued.

    Substitutions may be made at any time. No-shows will be charged the full amount.

    We discourage onsite registrations, however if you wish to register onsite, payment to happen through credit card immediately or check to be submitted onsite. Conference material will be given on the spot if it is available after distributing to other attendees. In case it is not available, we will send the material after the conference is over.

    In the event ComplianceOnline cancels the seminar, ComplianceOnline is not responsible for any airfare, hotel, other costs or losses incurred by registrants. Some topics and speakers may be subject to change without notice.

    Attendance confirmation and documents to carry to the seminar venue:
    After we receive the payment from the registered attendee, an electronic event pass will be sent to the email address associated with the registrant 5 working days before the seminar date. Please bring the pass to the venue of the event.

    Conference photograph / video:
    By registering and attending ComplianceOnline conference, you agree to have your photographs or videos taken at the conference venue and you do not have any objections to ComplianceOnline using these photos and videos for marketing, archiving or any other conference related activities. You agree to release ComplianceOnline from any kind of claims arising out of copyright or privacy violations.

    Offers:

  • Early bird seats are limited and based on first-come, first-serve.
  • Multiple offers cannot be combined.
  • 1

    Kansas City, MO
    September 26-27, 2019

    Hotel

    Sheraton Suites Country Club Plaza
    770 W 47th Street
    Kansas City, MO 64112, USA

    Tel: +1-816-931-4400

    How to Reach

    General Driving Directions:

    Driving directions from Kansas City International Airport
    • Get on I-29 S/US-71 S in May from International Cir, Cookingham Dr and NW 120th St,
    • Continue on I-29 S to Gallatin Township.
    • Take the MO-9 S exit from US-169 S, Get on I-35 S/I-70 W/US-24 W in Kaw Township.
    • Continue on I-35 S to Summit St/SW Trafficway.
    • Take exit 1A from I-35 S, Continue on SW Trafficway. Drive to Summit St

    Disclaimer: Directions to the venue above have been taken from the hotel website. Attendees are advised to check with the hotel for confirmation of these directions before starting for the venue. ComplianceOnline is not responsible for any inaccuracies in the same.

    2

    Chicago, IL
    December 5-6, 2019
    (Venue to be announced shortly)

    Register by phone or need assistance? Call +1-888-717-2436 Register Now Download Brochure

    We are pleased to offer several exhibitor, sponsorship and media partnership options designed to maximize your company's exposure and networking opportunities before, during and after the event.

    Benefits of becoming a Sponsor/Exhibitor/Media Partner:

    • Logo on website, marketing email, branding materials & the registration booth
    • Exhibit Space
    • Free event pass
    • Speaking opportunity
    • Social media campaign

    For more details and other sponsorship options at this event, please contact Event Manager: customercare@complianceonline.com or call: +1-650-238-9656

    Media Partner:

    Media Partner


    Pharmaceutical-Tech is essentially a B2B online business, technology media platform and global magazine that have under its wraps the largest global database of Pharmacy buyers and suppliers. We cover in-depth trends that shape industry dynamics and metamorphose global economics. Pharmaceutical tech has created a recognition that spans over a global audience, thereby revolutionizing how businesses transact.

    Register by phone or need assistance? Call +1-888-717-2436 Register Now Download Brochure

    Local Attractions of Kansas City, MO

    Country Club Plaza

    Country Club Plaza

    With amazing shops, great restaurants and those famed Kansas City fountains, the world famous Country Club Plaza gets the top pick of About Kansas City's attractions and destinations. The Plaza (as locals call it) was the US's first outdoor shopping, dining and entertainment district and is wonderful any time of year.

    Nelson - Atkins Museum of Art

    Nelson - Atkins Museum of Art

    The world renowned Nelson-Atkins Museum of Art (4525 Oak) is one of Kansas City's most treasured gems. With amazing exhibits both inside and out--the Nelson-Atkins boasts one of the most impressive collections anywhere. With everything from ancient Egyptian sculptures and Japanese collection with more than 2,000 works of art ranging from the 10th century B.C.E. you could spend days looking at everything.

    Worlds of Fun

    Worlds of Fun

    Worlds of Fun is the premier amusement park destination in the Midwest, offering 235 acres of excitement and fun for every member of the family, including the newly renovated Oceans of Fun. Come to Worlds of Fun to ride on & slide on all day long.

    Kansas City Zoo

    Kansas City Zoo

    The Kansas City Zoo and its adjoining IMAX Theater is a great attraction for those young and old alike. The Zoo has gone through a major transformation in the last few years and boasts over 200 acres with over 900 animals.

    Union Station/ Science City

    Union Station/ Science City

    The fully restored Union Station is one of Kansas City's favorite attractions with plenty of great things to see and do. With everything from the fully interactive Science City and its famed Rail Exhibit to movies, planetarium shows and world famous exhibits (think Dead Sea Scrolls and Titanic). They've also got some great restaurants like the famed Pierpont's and the Union Cafe if all that attraction going makes you hungry.

    Liberty Memorial and the National WW1 Museum

    Liberty Memorial and the National WW1 Museum

    Liberty Memorial and the WWI museum is the United States official WWI Museum and honor those who served in WWI and honor the memory of the sacrifices those who served made. This interactive exhibit shows the consequences WWI had and the impact it had on the US as a country. The museum and memorial serve as the leading educational institute and resource of WWI. Head to the top of the Liberty Memorial for some of the best 360 view of Kansas City.

    Local Attractions of Chicago, IL

    Windy

    Windy

    One of the more breathtaking scenes on the lake is this tall ship approaching the docks at Navy Pier. The 148-foot four-masted schooner (and its new sister ship, the Windy II ) sets sail for 90-minute cruises two to five times a day, both day and evening. (Because the boats are sometimes booked by groups, the schedule changes each week; call first to confirm sailing times). The boats are at the whims of the wind, so every cruise charts a different course. Passengers are welcome to help raise and trim the sails and occasionally take turns at the ship's helm (with the captain standing close by). The boats are not accessible for people with disabilities.

    Adler Planetarium and Astronomy Museum

    Adler Planetarium and Astronomy Museum

    The building may be historic (it was the first planetarium in the Western Hemisphere), but some of the attractions here will captivate the most jaded video-game addict.
    Your first stop should be the modern Sky Pavilion, where the don't-miss experience is the StarRider Theater. Settle down under the massive dome, and you'll take a half-hour interactive virtual-reality trip through the Milky Way and into deep space, featuring a computer-generated 3-D-graphics projection system and controls in the armrest of each seat. Six high-resolution video projectors form a seamless image above your head -- you'll feel as if you're literally floating in space. If you're looking for more entertainment, the Sky Theater shows movies with an astronomical bent; recent shows have included Secrets of Saturn and Mars Now!

    Arlington International Racecourse

    Arlington International Racecourse

    With its gleaming-white, palatial, six-story grandstand and lush gardens, this racecourse is one of the most beautiful showcases for thoroughbred horse racing in the world. Its storied history stretches back to 1927, and such equine stars as Citation, Secretariat, and Cigar have graced the track. The annual Arlington Million (the sport's first million-dollar race, held in mid-Aug) attracts top jockeys, trainers, and horses and is part of the World Series Racing Championship, which includes the Breeders Cup races. Arlington's race days are thrilling to behold, with all of racing's time-honored pageantry on display -- from the bugler in traditional dress to the parade of jockeys.

    Art Institute of Chicago

    Art Institute of Chicago

    You can't -- and shouldn't -- miss the Art Institute. (You really have no excuse, since it's conveniently located right on Michigan Ave. in the heart of downtown.) No matter what medium or century interests you, the Art Institute has something in its collection to fit the bill. Japanese ukiyo-e prints, ancient Egyptian bronzes, Greek vases, 19th-century British photography, masterpieces by most of the greatest names in 20th-century sculpture, and modern American textiles are just some of the works on display, but for a general overview of the museum's collection, take the free "Highlights of the Art Institute" tour Saturday and Sunday.

    Register by phone or need assistance? Call +1-888-717-2436 Register Now Download Brochure

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