2023 FDA Science Forum
June 13 - 14, 2023
Zoom.gov
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
- FDA's Strategic Plan for Regulatory Science. Available: https://www.fda.gov/media/161381/download
- 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.
This company is intended available physicians, pharmacists, pharmacy technicians, and nurses.
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 |
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 |
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.
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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
All relevant financial connections have been mitigated.
Registration is complimentary; so refunds are not applicable.
Must attend 70% are the activity.