Implications for Registration and Approval of Innovative Technologies

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Implications for Registration and Approval of Innovative Technologies Donald A. Prater, DVM Deputy Director U.S. FDA Europe Office Steven D. Vaughn, DVM & William Flynn, FDA, Center for Veterinary Medicine Presented at: OIE Global Conference on the Responsible and Prudent Use of Antimicrobial Agents for Animals March 14, 2013 Paris, France *This presentation reflects the views of the author and should not be construed to represent FDA s views or policies. It does not serve to bind FDA, nor confer any rights, privileges, benefits, or immunities for or on any person(s).

Four Critical Standards for Evaluating Veterinary Drugs Safety Human Food Target Animal Environmental User Safety Effectiveness Quality Manufactured Product Properly Labeled Product

Our public health mission succeeds when we put in the hands of the user: an approved, safe and effective, quality manufactured, properly labeled new animal drug to meet therapeutic and production needs of animals Core Mission

Core Mission Meeting the Therapeutic and Production Needs of Animals For companion animals: increase the level of high quality medical care for companion animals increase in quality of life through medical interventions for companion animals impact of animal health on the Human-Animal Bond

Core Mission Meeting the Therapeutic and Production Needs of Animals For food-producing animals: improve animal welfare and health improve animal health and production toward increasing the availability of an affordable, abundant and wholesome food supply to meet the needs of a growing human population

The Challenge Feeding People Ensuring an Affordable and Adequate Food Supply to Prevent Hunger is a Public Health Mission This is both a domestic and an international challenge

Status of Veterinary Drug Development Concern over antimicrobial resistance Limited development of new antimicrobials Increase in novel alternatives to antimicrobials Concern over antiparasitic drug resistance

Status of Veterinary Drug Development Change in Pharmaceutical Company Portfolios Increase in non-traditional entities Biotechnology, nanotechnology, immunological drugs For food animals more production enhancing indications and indications for environmental sustainability For non-food producing animals more non-traditional indications Chronic disease treatments, cancer therapy, life quality enhancements

Future Animal Health Environment New products will more likely come from acquisitions than discovery. CVM will work with more venture capital companies. Further consolidation/tighter financial accountability is highly likely. The future animal health industry will consist of a few large animal health companies, numerous small venture firms and coalitions of individual public and private organizations. More sponsors will be global firms and many will be from outside of the U.S.

Our Challenge To engage in the development and evaluation of new animal drugs, especially new innovative technologies, to meet the demand for increased safe, affordable and abundant food production

Future Animal Health Environment The products of the future may not fit the current paradigm. Products of the future will deploy new technologies for which we are just beginning to consider the critical safety and effectiveness standards for evaluation

As the industry changes so must we New Model for Success Challenge to efficiently adapt our policies and review approaches to meet new technologies Employ new scientific approaches to proving safety and effectiveness Provide predictability in regulatory decisions Avoid the lure of increasing scientific rigor beyond that which is necessary Address ambiguity

CVM s Innovation Initiative Is An attempt to position CVM where it needs to be in the future An attempt to work smarter at engaging new technology An attempt to move forward when the status quo is not meeting our needs Based on trust that people have good intentions and talent to make this happen

Innovation Initiative CVM created and is implementing processes to enable global availability of safe, effective, quality manufactured, properly labeled new animal drugs. Working with international partners, CVM is addressing challenges in a global animal health environment to meet our public health mission. CVM re-designed its drug evaluation process for new technologies to enable new technologies to reach the market to impact these public health challenges on a global basis. Overcome obstacles to ensure access to veterinary drugs and their proper use in food-producing animals.

What s the Win? Develop new approaches and engagement to enable a new technology to be met with the same predictability and seamless regulatory process that a traditional animal drug meets at CVM Remove barriers that prevent a pharmaceutical company from filling their pipeline with new innovative products

Extensive Scientific Interaction between Sponsor and CVM Agree on Specific Risk Questions and Plan for Answers Predictable/ Seamless Reviews Continued Evaluation of Safety and Effectiveness Knowledge Acquisition Formulation of Risk Questions Review Process Conditional Approval (Phase IV) Data Collection TECH TEAM Risk Analysts REVIEW TEAM Current Review Process Discovery/ Proof of Concept Development Regulatory Submission Launch Marketing Sponsor Decision To Develop Product Presubmission Conference NADA Approval

Global Animal Health - Current Activities OIE Collaborating Center in International Cooperation to Strengthen Veterinary Drug Regulatory Infrastructure Codex Alimentarius Commission VICH Inter-governmental Coordination Outreach World Organization for Animal Health (OIE) Food and Agriculture Organization (FAO) National and Regional Capacity Building Efforts

Global Animal Health - The Future What challenges in a global animal health environment have to be addressed to meet our public health mission? Are we adequately addressing the challenges of the future? What steps need to be taken to enable new technologies to reach the market to impact these public health challenges? What obstacles need to be overcome to ensure access to veterinary drugs and their proper use in foodproducing animals?

Global Animal Health - The Future What regulatory structures/approaches need to be developed and enhanced to enable the expansion of food production? What has to be initiated and what needs to be changed to meet the needs of the future? What is/are the necessary venues for us to intentionally and aggressively meet these new challenges internationally?

Questions???