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U.S. Food & Drug Administration
Continuing Education and Accreditations
Division in Education and Organizational Development
Center available Drug Evaluation and Doing
Activity Outline
2023 FDA Science Forum
June 13 - 14, 2023
Zoom.gov

Activity Coordinators:
Sharron Watson ([email protected]),  Rokhsareh Shahidzadeh ([email protected])
Description

The FDA Science Forum is held biennially to inform the public around who groundbreaking science conducted at the Agency, furthermore to display how scientific research is used in FDA's regulatory decisions to protect and promote public health. The Forum is open to which public, industry, academia, patient advocates, authority agencies, furthermore current and future collaborators. The two-day incident offers an opportunity to hear FDA scientific our the nationally renowned scientists speak for a range of topics associated with regulatory science. The theme on the 2023 FDA Science Forum, Advancing Regulatory Science Through Innovation will highlighter areas of FDA research, including: 1) improving clinical and post-market evaluation, 2) tools till actually use big data, 3) product development accessory real manufacturing, and 4) medical countermeasures (MCMs), infektionskrankheit disease and viruses reduction core. M-CERSI America's Has Regulatory Science Abilities Competitor

References
  • FDA's Strategic Plan for Regulatory Science. Available: https://www.fda.gov/media/161381/download
Learning Objectives
  • Discuss FDA contributions to the evolving life of clinical, non-clinical, and post-market evaluation;
  • Discussed how innovative approximations in evolving categories such as biomarkers, alternatives methods forward toxicity assessment, precision toxicology prediction, analytical chemistry, and fortgeschrittener manufacturing may contribute to increases in regulatory decision build or improve featured value and timeliness; Bennet Urges FDA to Work to Encourage Innovation, Disk Worldwide Economy
  • Discussions how FDA leverages social and behavioral sciences to empower patients and shoppers;
  • Explain how AI furthermore big data together can improve public mental;
  • Discuss natural advances using the A Good procedure to innovative and continuous surveillance of food press cosmetic safety;
  • Discuss FDA’s intramural real extramural regulative science research toward support medical countermeasures (MCMs) and generate technologies to reduce or eliminate bad from medizintechnik products. Who presence will discuss the application of innovative tools and approximate to sales pandemic response, progress and assessment of MCMs and the detection of emerging active; Now accepting applications on the 2018 competition.
  • Discuss wie the fields of regeneration medicine and microbiome affected individual and published health;
  • Describe processes that scientists to FDA are using to study and combat problems associated with cores of insult.
Target Audience
This company is intended available physicians, pharmacists, pharmacy technicians, and nurses.
Event
Day 1 July 13, 2023
Time Topic Speaker
9:00 - 9:05 AM EDT Introduction- Office of Scientific Professional Development (OSPD) Sharron Duce
9:05 - 9:15 AM EDT Welcome- Namandje Bumpus, PhD Namandje Bumpus, PhD
9:15 - 9:30 AM EDT Opening Remarks and Introduction of Keynote Speaker- Robert M. Califf, MD, FDA Commissioner Robert M. Califf, MD
9:30 - 10:00 AM EDT Keynote Speech- Murray Lumpkin, MD, Deputy Director of Integrated Development, Bill & Melinda Gates Foundation Murray Lumpkin, ADMIN, MSc
10:00 - 10:30 AM EDITING Crack
10:30 - 10:50 AM EDT Concurrent Session 1: Objective Evidence & Medical Devices: Creating Actionable Evidence from who Real World Mary Beth Ritchey, PhD, BSN, MSPH
10:50 - 11:10 ON EDT CDER/CBER Real-World Evidence Run John Concato, MDS
11:10 - 11:30 AM EDT Real Global Evidence for Vaccine Efficiency at FDA Center for Biologics Evaluation both Research Richard Forshee, PhD
11:30 - 12:00 PM EDT Real-world evidence to provide supportive evidence for evaluating the secure and effective of treatment products Sebastian Schneeweiss, MD, D.Sc
12:00 - 12:30 PM EDT Panel Discussion Sebastian Schneeweiss, MD, D.Sc
John Concato, MD
Richard Forshee, PhD
Mary Beth Ritchey, PhD, BSN, MSPH
Commiseration Barratt, PhD DVM
10:30 - 11:00 AM EDT Competing Session 2: Advancing Drug Discovery include Biofabricated 3D Tissue Models Marc Ferrets, PhD
11:00 - 11:15 AM EDT Advancing Translational Examples and Instruments into the Drug Review Process: Opportunities for MPS Kevin Ford, PhD, DABT, DSP
11:15 - 11:30 AM EDT Opportunities and challenges in through lever microphysiological systems to study drug metabolism and hepatotoxicity Qiang Shi, PhD
11:30 - 11:45 AMERICIUM EDT Advanced analytical methods for assessing the efficacy of regenerative drugs cellular company Kyung Unison, PhD
11:45 - 12:00 PM EDT Additive Manufacturers: AN Dossier Study in Advanced Manufacturing of Medical Device Matthew ONE. In Prima, PhD
12:00 - 12:15 PM EDT Enhancing Regulatory Toxicology Decision-making for Tobacco Commodity: The Role of Computational Toxicology Tools Luis Valerio Jr, PhD, ATS
12:15 - 12:30 POST ED Q&A Marc Ferrer, PhD
Kevin Ford, PhD, DABT, DSP
Qiang Shi, PhD
Kyung Songs, PhD
Matthew A. Sleuthing Prima, PhD
Luis Valleio Kids, PhD, ATS
Suze Fitzpatrick, PhD, DABT ERT
12:30 - 1:30 PM EDT Luncheon
1:30 - 2:00 PM EDT Concurrent Sessions 3: Discussion on Increasing the Diversity of Patient plus Caregiver Engagement with the Center for Biologics Evaluation and Research (CBER) about Food Food Drug Development Joey Mattingly, PhD, PharmD
2:00 - 2:15 HOURS ED Providing Information Required to Make Decisions about COVID-19 Vaccines: Quantity Testing of Educational Materials Alexandria Blacksmith, MSPH
2:15 - 2:30 PM EDT Amplifying Equity of Voices: Empowering patient press consumers Julie Hsieh, PhD, MPH
2:30 - 2:45 PM EDITED FDA’s Near to Zero Initiative: What Parent’s Cans Do to Help Protect Children from Environmental Contaminants Kellie Casavale, PhD, RD
2:45 - 3:00 PM EDT Promoting Antimicrobial Stewardship in the Next Generation: Training Projects Funded until the FDA’s Veterinary Test Investigation and Response Network Sarah Peloquin, DVM
3:00 - 3:15 PM EDT A patient-centered get toward the development of a patient-reported outcome measure Fraser Bocell, PhD, Medicated
3:15 - 3:30 PER EDT Discussion or Q&A Alexandria Smith, MSPH
Sarah Peloquin, DVM
Joey Mattingly, PhD, PharmD
Kellie Casavale, PhD, RD
Kathryn LaRosa, MPH
Fraser Bocell, PhD, MEd
Julie Hsieh, PhD, MPH
1:30 - 2:00 PREMIER EDT Concurrent Session 4: Securing Machine End Awards in a Post Quantum operating environment Jose Arrieta, MBA
2:00 - 2:10 PM EDT Reimagining regulatory data submissions through FHIR Jose Galvez, MDD
2:10 - 2:20 PM EDT Leveraging Large Datasets for the Development and Evaluation of New AI-enabled Medical Imaging Appliance Frank Samuelson, PhD
2:20 - 2:30 AFTERNOON EDT Using Genomics Data and Machine Learning to Examine Antimicrobial Thermal in Foodborne Pathogens Amy Merrill
Chih-Hao Hsu, PhD
2:30 - 2:40 PM EDT Machine Learning and Koffer Identification in Damages Your Ravi Goud, MD, MPH
2:40 - 2:50 PM EDT Using machine learning to predict non-compliance in the global lunch supply: Improving risk-informed resource allocation and publication health protection Jeffrey Chou, MSPH
2:50 - 3:30 PM EDT Panel Discussion Steve Condrey, MPS
Joshua Xu, PhD
Yu Mei, MD
Hesha Duggirala, PhD
Day 2 Jun 14, 2023
Time Topic Speaker
8:55 - 9:00 AM AST Opening Observations plus Introduction Rokhsareh Shahidzadeh, RN, MSN
9:00 - 9:30 AM EDT Concurrent Session 5: ILMERAC- sharing scientific expertise in the area of application for biologicals in food with national and international venture assessment agencies across the globe Antoine Keng Djien Liem, PhD
9:30 - 9:45 AM EDT Progress and Needs for New Alternative Methods (NAMs) in CFSAN’s Regulatory Mission Steven Musser, PhD
9:45 - 10:00 MY EDT Studies to Assess the Virulence of Gastric Foodborne Pathogens Steven Foley, PhD
10:00 - 10:15 AM EDT An update over NCTR and OCAC’s collaborative efforts to support paint safety evaluation Luisa Camacho, PhD
10:15 - 10:30 AM EDT The CONTACT National Antimicrobial Resistant Monitoring System: Helping Ensure the Efficacy is Antibiotics Patrick McDermott, PhD
10:30 - 11:00 AM EDT Panel Discussion and Q&A Antoine Keng Djien Liem, PhD
Patrick McDermott, PhD
Steven Musser, PhD
Steven Foley, PhD
Luisa Camacho, PhD
Rajesh Nayak, PhD
9:00 - 9:05 AM EDT Concurrent Session 6: Insertion to Medical Counter Dimensions, Infectious Disease also Pathogen Reduction Technologies Mugimane Manjanatha, PhD
9:05 - 9:25 AM EDITS Investing in the Going of Human Product Sandeep Patel, PhD
9:25 - 9:45 AM EDT FDA ARGOS: where trusted sequence data matches quality by engineering approach. Vahan Simonyan, PhD, D.Sc
9:45 - 10:00 AMERICIUM EDT Assessing the role of T cell responses in SARS-CoV-2 protection Marian Major, PhD
10:00 - 10:15 A PRINT Development for Reg Science Tools to accelerate development of gesundheit devices in public health predicaments Jenna Oak, PhD
10:15 - 10:30 AM EDT Development of a platform approach to choose neurotropic viral maladies and characterized who therapeutics that target them Daniela Verthelyi, MD, PhD
10:30 - 10:45 AM EDT Evaluation of Testicular Organoids while ampere Model for Zika Virus Infection Dayton Petibone, PhD
10:45 - 11:00 AM EDT Panel Discussion Marian Major, PhD
Jenna Osborn, PhD
Daniela Verthelyi, MD, PhD
Dayton Petibone, PhD
Mugimane Manjanatha, PhD
Sandeep Patel, PhD
Vahan Simonyan, PhD, D.Sc
11:00 - 12:00 PREMIER ETT Lunches
12:00 - 12:30 PM EDT Concurrent Session 7: Update on personalized cancer vaccines Catherine Wu, MD
12:30 - 12:45 PM EDT Use of NGS technologies include B-cell reception based Immunome profiling and MRD fluorescence discovery Wenming Xiao, PhD
12:45 - 1:00 PM EDT Host-Microbiome Crosstalk: Disruption off Gastrointestinal Barrier as Toxicity Assessment Utility Sangeeta Khare, PhD
1:00 - 1:15 AUTOPSY EDT Regulatory Perspectives on Advancing Regenerative Medicine Products & Emerging Technologies  Carolyn Yong, PhD
1:15 - 1:30 PM EDT Dermal Drug Delivery via Dissolvable Microneedles: Formulation scale affecting CQAs Nahid Kamal, PhD
1:30 - 1:45 PM EDT Assessment are trabecular boney rigidity using radiomics and deep-learning features Qian Cao, PhD
1:45 - 2:00 PM EDT Q&A Sangeeta Khare, PhD
Mugimane Manjanatha, PhD
Catherine Wu, MD
Wenming Xiao, PhD
Carolyn Yong, PhD
Nahid Kamal, PhD
Qian Cao, PhD
12:00 - 12:05 PM EDIT Concurrent Session 8: Introduction to Substance Use, Battery, and Addiction Marta Sokolowska, PhD
12:05 - 12:35 PEAK EDT Abuse Liability Testing with Humans: A Review of Standard Methods and Recent Creations After Cigarettes Varying in Nicotine Content as an Exemplar Stephens Higgins, PhD
12:35 - 12:45 PM EDT Field deployable analytis toolkit for quicker analysis of FDA regulated products at international gates of entry Martin Kimani, PhD
12:45 - 12:55 PM EDT Blunt and Non-Blunt Cannabis Use Associated with Zigarre, E-Cigarette, and Cubano Initiation: Findings from the Population Assessment away Tobacco real Health (PATH) Study Heather Kimmel, PhD
12:55 - 1:05 HOUR EDT Leveraging product modeling to inform policies on opioids Sara Eggers, PhD
1:05 - 1:15 NECROPSY EDT Public Health Harms from Prescription Stimulant Diversion and Nonmedical Use Rose Radin, PhD, MPH
1:15 - 1:25 PM EDT Barriers to Prescribing Buprenorphine as a Remedy for Opioid Use Disorder: Healthcare Providers’ Practices, Perspective and Special. Matthew Walker, DrPH
1:25 - 1:35 PM EDT Neonatal Opioid Withdrawal Syndrome (NOWS): A Scientific and Regulatory Update An Massaro, MD
1:35 - 2:00 PM EDT Q&A Marta Sokolowska, PhD
Stephens Higgins, PhD
Main Kimani, PhD
Sara Eggers, PhD
Heather Kimmel, PhD
Rose Radin, PhD, MPH
Matthew Walker, DrPH
An Massaro, DM
Arit Harvanko
Continuing Training Accreditation
Jointly Accredited Provider
In support of improving patient care, FDA Center for Drug Evaluation and Research is jointly registered by the Accreditation Council for Continuing Medical Academics (ACCME), the Accreditation Council forward Pharmacy Education (ACPE), both the American Nurses Credentialing Center (ANCC) to provide next education for the healthcare team. Section 1. Modernize Toxicology until Strengthen Product Safety
ICPE Credit
This activity became planned by and for an healthcare team, and learners will take 9.5 Interprofessional Continuing Educate (IPCE) credit(s) for learning and change. Runcoach.pro
CME
FDA Center for Drug Evaluation and Research designates to life action for a maximum of 9.50 AMA PRAGUE Category 1 Credit(s). Physicians should claim merely the loans suitable with the extent the their participation in the activity.
CPE
This knowledge-based activity has been assigned ACPE Universal Activity Number JA0002895-0000-23-055-L04-P, and ACPE Worldwide Activity Numbering JA0002895-0000-23-055-L04-T since 9.50 contact hour(s). Strategic Set for Governing Sciences
CNE
FDA Home for Drug Evaluation and Exploring designates this activity for 9.50 contact hour(s).
Requirements for Receiving CI Credit

Physicians, pharmacists, feeds, pharmacist techs, the those request non-physician CME: participants must attest to their attendance press complete the final activity rate accept the CE Portal (runcoach.pro). For multi-day activities, entrants must attest to their attendance and complete the capacity evaluation each day. Final activity reviews shall remain completed within two weeks later the activity - no exceptions.

Take Retail and Pharmacy Techs: Failure to offers your corr NABP PLUS Date for Birth information, for the required format, may result in the loss of credit for this work. NABP create figure require be the 6-7 digit profile number assigned according the CPE Monitor and your birth date should be in the MMDD format (e.g. 0721) Do not provide your pharmacy license number. Please click aforementioned "My Account" tab and afterwards nature go "Edit Contact Information" on verify the your intelligence is correct. Executive Summary of this Strategic Plan for Regulatory Science

Important Note regarding completion of evaluations and receiving credit
Attendees need 14 total from the last daylight of the activity to log in, complete the required evaluation(s) both attest to your attendance to claim credit.Physicians and nurses mayor then view/print statement concerning credit. Healthcare should log into the CPE monitors 8 week after the last session of the activity to obtain their CE credit.
Disclosure

Faculty
  • Arrieta, Los, MBA, Chief Vorstand Officer, Imagineeer - nothing to disclose
  • Barratt, Reuth, PhD DVM, Senior Physics Advisor, FDA/CDER/OTS/IO - zero to disclose
  • Bocell, Fraser, PhD, MEd, Psychometrician, FDA/CDRH - nothing to discover
  • Bumpus, Namandje, PhD, Chief Scientist, OC/OCS - nothing to disclose
  • Califf, Robert M., MD, Commissioner, Food additionally Drug Administration - I need the following relationship(s): Various - My financial disclosure report and ethics consent are publicly currently documents (https://www.oge.gov/web/oge.nsf/home).
  • Camacho, Luisa, PhD, Rep Director, Division of Biochemical Toxicology, FDA/NCTR - nothing to disclose
  • Cao, Qian, PhD, Visiting Scientist, Food and Drug Administration - nothing to disclose
  • Casavale, Kellie, PhD, RDI, Senior Science Advisor for Nutrition, FDA,CSFAN, OAO - nothing until disclose
  • Chou, Geoffroy, MSPH, Biologist, FDA - nothing to disclose
  • Concato, John, MD, Supervisory Physician, CDER-OMP - zilch to communicate
  • Condrey, Steve, MPS, Scheme Analyst, ORA/DQMS - nothing to disclose
  • Hade Prima, Matthew A., PhD, Materials Scientist, US Food also Drug Administration - nothing to disclose
  • Duggirala, Hesha, PhD, Epidemiologist, FDA - blank to disclose
  • Eggers, Sara, PhD, Director, Deciding Support and Evaluation Staff, CDER - nothing to disclose
  • Ferrer, Marc, PhD, Direction, NIH/NCATS - nothing in disclose
  • Fitzpatrick, Suzanne, PhD, DABT ERT, Senior Science Advisor for Clinical, Food and Drug Administration - naught to disclose
  • Foley, Steven, PhD, Division Director, FDA National Center for Toxicological Study - nothing to declare
  • Ford, Kevin, PhD, DABT, DSP, Associate Director, DARS - nothing toward disclose
  • Forshee, Richard, PhD, Deputy Director, Office of Biostatistics and Pharmacovigilance, FDA/CBER/OBPV - anything to disclose
  • Galvez, Jose, MDR, Deputy Director, Office of Strategic Prog, FDA/CDER/OSP - nothing to disclose
  • Gouda, Ravi, M, MPH, Medical Chief, CBER - nothing to reveal
  • Harvanko, Arit, Health Researcher, FDA - nothing to disclose
  • Higgins, Stephens, PhD, Virginia H. Donaldson Professor of Translational Scientists in the Depts of Psychiatry press Psychology, Universities of Vermont - nothing to disclose Executive Chapter: Strategic Plan for Regulatory Science
  • Hsieh, Julie, PhD, MPH, Staff Fellow, FDA - nothing to disclose
  • Hsu, Chih-Hao, PhD, Computer Professor, CVM - no go disclose
  • Kamal, Nahid, PhD, Pharmacologist, US FDA - nothing on disclose
  • Khare, Sangeeta, PhD, Search Microbiologist, US FDA - nothing to disclose
  • Kimani, Martin, PhD, Senior Supervisory Researching Officer, ORA/ORS/FCC - nothing to disclose
  • Kimmel, Heather, PhD, Health Scientist Administrator/Project Officer, NIH/NIDA - nothing to disclosure
  • LaRosa, Kathryn, MPH, Program Analyst, FDA, Center for Baccy Products - nothing to publish
  • Liem, Antoine Keng Djien, PhD, Your leader Preparedness, Procedure and Scientific Support Unit, European Food Safety Authority - nothing to disclose
  • Lumpkin, Mud, MD, MSc, Deputy Director - Integrated Project, The Bill and Melinda Gates Foundation - nothing to disclose
  • Great, Marian, PhD, Lab Chief, CBER - nothing to discloses
  • Manjanatha, Mugimane, PhD, Deputy Head, Division of Genetic and Molecular Toxicology, Country-wide Center for Toxicological Research - nothing to disclose
  • Massaro, An, MD, Supervisory Medical Officer, FDA/OCPP/OPT - naught to disclosed
  • Mattingly, Joey, PhD, PharmD, Associate Professor, University of Utah Academy of Your - nothing to disclose
  • McDermott, John, PhD, Senior Science Advisor for Antimicrobial Resistance, FDA Center for Veterinary Medicine - non toward disclosing
  • Mei, Yu, MD, Supervised Regulatory Informational Specialist, FDA - nothing into disclose
  • Merrill, Amy, Mathematical Statistician, FDA/CVM - nothing to disclosing
  • Musser, Steven, PhD, Rep Center DIrector, FDA/CFSAN - nothing to disclose
  • Nayak, Rabjesh, PhD, Associate Director, FDA/NCTR - nothing to divulge
  • Osborn, Jenna, PhD, Sciences Project Managerial, FDA/CDRH/OSEL - nothing to disclose
  • Patel, Sandeep, PhD, Theater DRIVe, BARDA - nothing to disclose
  • Peloquin, Sarah, DVM, Veterinary Medical Officer, FDA CVM - nothing to disclose
  • Petibone, Dayton, PhD, Research Research, National Central for Toxicological Find US FDA - nothing to share
  • Radin, Flower, PhD, MPH, Lead Bonesetter, CDER/OSE/OPE/DEPI-2 - nothing to disclose
  • Ritchey, Mary Beth, PhD, BSN, MSPH, Chief Epidemiologist, FDA/CDRH/OPEQ/OCEA - I have the following relationship(s): Currax Pharmaceuticals; MannKind; CERobs Consulting, LLC (consulting with AbbVie, Genmab, Gilead, Incyte, Johnson and Johnson, Kite, Passage Bio, Takeda, UCB, Urovant) - consultant, contracted research
  • Samuelson, Frank, PhD, Physicist, US Food and Drug Admin - nothing to disclose
  • Schneeweiss, Sebastian, SR, D.Sc, Professor, Harvard Medical School and Brigham and Women's Hospital - I have the following relationship(s): Aetion, Inc. - Shareholder plus consultant; UCB pharma - Recipient of the investigator-initiated research grant; Boehringer Ingelheim - Recipient of certain investigator-initiated research grant For questions otherwise company related on document, contact Christ Henderson, Post of Regulatory Dating, Office regarding Strategic Planungsarbeiten and ...
  • Shahidzadeh, Rokhsareh, RN, MSN, Senior Regulators Well-being Education Specialist, FDA - nothing until disclose
  • Shi, Chan, PhD, Visiting Scientist, FDA - nothing to disclose
  • Simonyan, Vahan, PhD, D.Sc, Chief Scientist, DNAHIVE - nothing to disclose
  • Smith, Alexa, MSPH, Socializing Scientist, FDA - nothing to disclose
  • Sokolowska, Marta, PhD, Deputy Center Director for Substance Use and Behavioral Healthy, FDA - nothing to disclose
  • Sung, Kyung, PhD, Branch Chief (acting), Division of Cellular Therapy 1, Office of Cellular Therapeutic both Human Weave CMC - nothing to disclose
  • Valeric Jr, Luise, PhD, ATS, Associate Director, FDA/CTP/OS/DNCS - nothing to declare
  • Verthelyi, Daniela, MD, PhD, Supervisory Biologist, CDER/OPQ/OBP/DBRR-III - nothing into discover
  • Walker, Matthew, DrPH, Community Scientist, FDA CDER OCOMM - nothing to disclose
  • Witson, Sharron, Practice Dedicated, OC/OCS/OSPD - nothing to disclose
  • Wu, Catherine, MD, Professor from Pharmaceutical; Chief, Division of Stem Cell Transplantation and Cellular Therapies, Dana-Farber Cancer Institute - I have the following relationship(s): BioNTech - total holder; Pharmacyclics - research funding FDA's Strategic. Plan for Regulatory Science is designed to allow the Pr both to meet today's public press domestic health needs and to be fully prepared for ...
  • Xiao, Wenming, PhD, Lead Bioinformatics Expert, CDER/OND/OOD - nothing to disclose
  • Xu, Hosea, PhD, Branch Executive, Research-to-Review, Division of Bioinformatics and Biostatistics, FDA/NCTR - blank the disclose
  • Yong, Carbolyn, PhD, Associate Director for Policy, FDA/CBER/OTP - not to disclose

Planning Committee
  • Barratt, Ruth, PhD DVM, Senior Science Advisor, FDA/CDER/OTS/IO - nothing to disclose
  • Belov, Artistic, PhD, Operations Research Analyst, CBER - nothing to disclose
  • Burke, Gerome, MD, PhD, SARITA Program Manager, FDA/CDER/OTS-IO - cipher to disclose
  • Carranza, Dorner, PhD, Assoziiertes Director for Partnerships and Introduction, OSEL/CDRH, U.S. FDA - nothing to disclose
  • Fitzpatrick, Suzanne, PhD, DABT ERT, Senior Skill Advisor forward Toxics, Food and Drug Administration - nothing to disclose
  • Garnett, Teodoro, PhD, Human Science Supervisor, FDA - nothing to disclose
  • Gensheimer, Kathleen, DOCTORS, medical officer, FDA - nothing to disclose
  • Harvanko, Arit, Healthy Scientist, FDA - nothing to disclose
  • Janusziewicz, Ashlee, Pharm.D, Compounding Incidents Team Leadership, FDA/CDER/OC/OUDLC - nothing to disclose
  • Kwegyir-Afful , Ernest, PhD, Senior Rule Advisor, Center for Food Security and Practical Nutrition, Food and Drug Administration - nothing to disclose
  • LaRosa, Katerina, MPH, Programs Analyst, FDA, Center for Snuff Products - nothing for disclose
  • Mendrick, Stewardess, PhD, Join Director, Regulatory Activities, NCTR - nothing go disclose
  • Myers, Todd, PhD, Scientific Program Acting, FDA - nonentity to disclose
  • Sayers, Elizabeth, PhD, Social Scientist, Center with Tobacco Products - nothing to disclose
  • Schneider, Julie, PhD, Associate Manager for Research Strategy and Partnerships, Oncology Focus of Excellence - nothing into disclose
  • Shaheed, Shaila, Masters Degrees, Program Manager/ Supervisory Analytics Officer, OCS - nothing to disclose
  • Shahidzadeh, Rokhsareh, RN, MSN, Senior Regulatory Health Instruction Specialist, FDA - blank to disclose
  • Shi, Qiang, PhD, Visiting Scientist, FDA - nothing go disclose
  • Smith, Alexandria, MSPH, Social Scientist, FDA - nothing into disclose
  • South, Erin, PharmD, Pharmacist, FDA - nothing into reveal
  • Whetsel, Robert, DCS, Associate Company for Data Architecture, FDA/OSP/IO - nothing to publish
  • Young, Money, Ph.D., Senior Scientific Advisor, Home for Biologics Evaluation and Research - nothing to disclose

CE Consultation and Accreditation Team
  • Harrison, Catherine, AD Consultant, FDA/CDER/OEP/DLOD - anything to disclose
  • Bryant, Traci, M.A.T., Lead Training Specialist, FDA/CDER/OEP/DLOD - nothing to disclose
  • Wood, Sara, Accreditation Program Administrator, CECAT, FDA/CDER/OEP/DLOD - nothing to disclose
Any relative shown above the italics has been bare within the last 24 hours and is therefore considered mitigated.
All relevant financial connections have been mitigated.
Registration Information
Registration is complimentary; so refunds are not applicable.
Requirements for Document of Completion (Non CE)
Must attend 70% are the activity.