Course "An introduction to Veterinary Pharmacology" has been pre-approved by RAPS as eligible for up to 10 credits towards a participant's RAC recertification upon full completion.


This course is an introduction to Veterinary Pharmacology. It will provide background, context and understanding regarding Absorption, Distribution, Metabolism and Excretion (ADME). In addition, there will be a limited introduction into comparative physiology in the major veterinary species with each section. Finally, an introduction into Pharmacokinetics and the terminology used in this area will also be provided. This seminar will provide attendees with an understanding of Veterinary Pharmacology and ADME topics in the context of veterinary drug development.

Seminar Fee Includes:
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 have learned:

  • To gain a general understanding of all aspects of the basic science of Veterinary ADME/Pharmacokinetics.
  • To learn the vocabulary related to Veterinary ADME/Pharmacokinetics.
  • To understand the interactions of chemical compounds and living systems.
  • To appreciate how drug actions and interactions relate to physiological principles. Pharmacology is simply: PHYSIOLOGY OR PATHO-PHYSIOLOGY BEING INFLUENCED BY AN EXOGENOUS COMPOUND(S).

Who will Benefit:

This course is designed for people tasked with developing and maintaining an animal health company's product portfolio and who may also be involved with 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
  • Scientists in Veterinary Drug Development
  • Entrepreneurs and small business owners wanting to understanding Veterinary Pharmacology
  • CRO professionals
  • Entrepreneurs looking to add value to their products
  • Regulatory professionals
  • Process owners
  • Financial Advisors and Institutional Investors
  • Consultants, Inspectors and cGxP Experts
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Day 01(8:30 AM - 4:30 PM)
  • 08.30 AM - 09.00 AM: Registration
  • 09.00 AM: Session Start
  • Introduction to General Principles of Veterinary Pharmacology
  • Introduction
    • General Principles
    • Dosage Forms
      • Solid
      • Liquid
    • Route of Administration
      • Oral (PO)
      • Parenteral
        • IM
        • SC
        • IV
        • Topical
        • Other
  • Absorption
    • Dissolution
    • Movement across membranes
      • Blood flow
      • Solubility
      • Surface area
    • pH partitioning
    • Oral
    • IV
    • IM
    • SC
    • Topical
    • Intratracheal/Nebulization/Inhalation
  • Distribution
    • Movement across Membranes
    • Plasma Protein binding
    • Tissue concentrations
    • P-glycoprotein and other transporters
Day 02(8:30 AM - 4:30 PM)
  • Metabolism
    • Organs
    • Phase I
      • CYP
      • Oxidation
      • Reduction
      • Hydrolysis
    • Phase II
      • Glucuronidation
      • Acetylation
      • Sulfation
    • 1st pass effect
    • Species differences
  • Elimination
    • Routes
    • Renal
    • Intestinal
  • Pharmacokinetics
    • Concentration vs time curves
    • Compartmental vs non-Compartmental
    • Parameters
      • AUC
      • AUMC
      • Cmax
      • Tmax
      • t1/2
      • λ
      • Vd
      • Clp
    • Bioavailability (F)
    • Bioequivalence
    • Dosage regimens
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Rob Hunter

Rob Hunter
Veterinary Drug Development Specialist

Seminar Instructor Rob Hunter has 20 years of veterinary and human drug development experience with NASA, Pfizer, Elanco, Parnell, and Provetica. He has contributed to the approvals for Revolution®, Dectomax®, Ovugel®, and Pulmotil®, with others currently in development or under regulatory review. Internationally recognized subject matter expert on pharmacokinetics, antimicrobial PK/PD, interspecies allometry, drug metabolism, bioequivalence, and tissue residues/human food safety along with corresponding bioanalytical support. Dr. Hunter has served on and chaired several AHI committees and represented the U.S. veterinary pharmaceutical industry on the VICH bioequivalence expert committee. He has represented various companies at CVM/FDA, EMA/CVMP, APVMA, VDD (Canada), NVQRS/QIA (South Korea), Thailand FDA, NVAL (Japan), Ministry of Agriculture (Vietnam), and IVDC (China) regarding specific products, issues, and/or policies.

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