All times are in Singapore Time Zone (GMT +8)
Day 1 ─ Wednesday, 19 October, 2022
8:30 – 9:00
9:00 – 9:15
9:15 – 9:30
Registration
Opening address by Dr Tan Lee Kim, PPA(P), PPA(G), Director General (FA) of SFA
Pre-recorded remarks by Dr Robert M. Califf M.D, FDA Commissioner
Remarks by Dr. Weida Tong, Director, Division of Bioinformatics and Biostatistics, National Center for Toxicological Research (NCTR), U.S. Food and Drug Administration (FDA)
Plenaries: Emerging Regulatory Science Topics in Nanotechnology related to Food and Medical Products
Co-chairs: Dr. Anil Patri and A/Prof. Joanne Chan
Notetakers: Herman Teo, Ivan Ng
9:30 – 9:40
Co-chair Session Opening Remarks
9:40 – 10:10
Plenary 1: Global Regulatory Science and Standards Landscape of Nanotechnology for Medical Products and Food ( Dr Anil Patri)
Poster Room
10:10 – 10:40
Plenary 2: Nanotechnology and Food: EFSA’s approach to safety (Dr. George Kass)
Set-up
10:40 – 11:00
Coffee Break
11:00 – 11:30
Plenary 3: Nanotechnology in food – a food safety perspective (Ms. Angela Li)
11:30 – 12:00
Plenary 4: Nanotechnology and food - the regulatory approach taken 'down under’ (Mr. Steve J. Crossley)
12:00 – 12:30
Plenary 5: Initiatives for Safety Assessment of Nanomaterials at Center for Biological Safety and Research, National Institute of Health Sciences (Dr. Yoko Hirabayashi)
12:30 – 14:00
Lunch
Poster presenters to pin up their posters during lunch
Session 2: Innovation in Nanotechnology for FoodCo-Chairs: Prof. Wu Yong Ning, A/Prof. Benjamin Smith
Notetakers: Yong Quan, Patrick Gan
Session 3: Nanomaterials for Gene DeliveryCo-Chairs: Dr. Takao Inoue, Dr Luigi Calzolai
Notetakers: Lim Chew Leng, Wesley Yu
Poster Display
Location: Level 2, Rosewood Room & Nutmeg Room
14:00 – 14:10
Co-Chairs Session Opening Remarks
Co-Chairs Session Opening Remarks
14:10 – 14:40
Talk 1: Advances in the physicochemical characterization of nanoparticles in a regulatory context. Dr. Jan Mast
Talk 1: Development of prototype LNP vaccines for Lyme disease. Dr. Michael Johnston
14:40 – 15:10
Talk 2: Safety assessment of nanoparticles in food: Current status and prospective. Prof. Liu Ying
Talk 2: Characterization of nanovaccines for COVID-19. Dr. Luigi Calzolai
15:10 – 15:40
Talk 3: Selenium nanoparticles functionalized by mushroom polysaccharide-protein complex: A novel nano-mineral for managing postmenopausal osteoporosis. Prof Wong Ka Hing
Talk 3: Validation of the effects of transport on COVID-19 mRNA vaccines. Dr. Takenori Yamamoto
Poster display room is open for viewing
15:40 – 16:10
Coffee Break
16:10 – 16:40
Talk 4: Nanotechnology for Biomedical and Food Applications. Prof Jackie Y. Ying
Talk 4: Analytical technology and regulatory concerns of liponanoparticle medicine – Taiwan FDA’s experience sharing in reviewing and testing mRNA COVID-19 vaccines. Dr. Hsu Jiachuan
16:40 – 17:10
Talk 5: Polymer Nanocomposite for Sustainable Food Packaging. Dr. Li Xu
Talk 5: Modular and adaptive dendrimer nanovectors for nucleic acid delivery. Dr. Ling Peng
17:30 – 19:00
Drinks reception
All times are in Singapore Time Zone (GMT +8)
Day 2 ─ Thursday, 20 October, 2022
Poster Display:8:00—12:40, 14:00—17:30, Location: Level 2, Rosewood Room & Nutmeg Room
Session 4: Monitoring and characterization of Microplastics & NanoplasticsCo-Chairs: Dr. Wu Yuansheng, Dr. Josefa Barrero
Notetakers: Hui Yi, Yi Li
Session 5: Progress in Nanotechnology StandardsCo-Chairs: Dr. Shan Zou, Dr. Asa Jamting
Notetakers: Lian Jie, Wesley Yu
Bioinformatics Workshop
Notetakers: Jia Qi, Stan
8:00 – 8:30
Session 0: Welcome and Session Overview
(Dr. William Slikker Jr, Dr. Tong Weida)
8:30 – 8:40
Co-Chairs Session Opening Remarks
Co-Chairs Session Opening Remarks
AI4TOX – An FDA Artificial Intelligence (AI) program for toxicology, Dr. Weida Tong (NCTR/FDA, USA)
Session 1: Food and Drug Safety
Co-Chairs: Dr. George Kass (EFSA, Italy) and Dr. William Slikker Jr. (Former GCRSR co-chair, USA)
8:40 – 9:10
Talk 1: Micro-plastics and other emerging issues: an overview on the food safety implications. Dr. Vittorio Fattori
Talk 1: Micro-plastics and other emerging issues: an overview on the food safety implications. Dr. Vittorio Fattori
20 min for each item
Talk 1: Data science for food safety: how to integrate new streams of data in the risk assessment process?
9:10 – 9:40
Talk 2: Microplastics in typical seafood in China: current status and future perspectives. Prof. Wu Yong Ning
Talk 2: Current Progress and Standards Needs for Nanomedicines. Dr. Caterina Minelli
George Kass (EFSA, Italy)
Talk 2: Text Analytics for Food Safety Monitoring, Mr. Benjamin Er (National Centre for Food Science, SFA, Singapore)
9:40 – 10:10
Talk 3: Monitoring of microplastics in drinking water. Stepping stones of developing a methodology. Dr. Dora Mehn
Talk 3: Certified reference materials for lipid-based nano-delivery systems – development and unique challenges. Dr. Shan Zou
Talk 3: Use of Machine-Learning and Artificial Intelligence for Drug Toxicology, Dr. Peter Newham (Clinical Pharmacology and Safety Sciences, AstraZeneca, UK)
Talk 4: Data science in early derisking of drug targets and discovery chemistry, Dr. Ruth Roberts (University of Birmingham, UK)
10:10 – 10:20
Coffee Break
Talk 5: Panel Discussion and Q/A
10:20 – 10:40
Coffee Break
Session 2: Standards and Best Practice
Co-Chairs: Prof. Tim Gant (UK Health Security Agency, UK) and Dr. Maurice Whelan (JRC, European Commission)
10:40 – 11:10
Talk 4: Micro-/Nanoplastics (MPs/NPs) in Food: Analytical Developments and Challenges. Dr. Yu Dingyi
Talk 4: NMIA’s Nanometrology Section: Supporting accurate and reproducible nanotechnology research and commercialization. Dr. Åsa Jämting
20 min per item
Talk 1: Open, FAIR and reproducible science, Prof. Susanna Sansone (Oxford University, UK)
11:10 – 11:40
Talk 5: Monitoring and Characterization of Microplastics and Nanoplastics. Dr. Kay Ho
Talk 5: ISO standards on Nanotechnology and Nanomaterials. A/Prof. Lanry Yung Lin Yue
Talk 2: Taking omics from concept to application in chemicals regulation, Prof. Tim Gant, (UK Health Security Agency, UK)
11:40 – 12:10
Talk 6: Understanding the health risks from exposure to micro- and nanoplastics in food: an overview of CUSP’ perspective. Prof. Alba Hernández Bonilla
Talk 6: Development of National Nanotechnology standard and guidelines in Thailand. Dr. Thongkam Waluree
Talk 3: Reference materials and datasets for improved reproducibility, Dr. Yuanting Zheng (Fudan University, Shanghai, China)
Talk 4: Bridging scientific data with evidence needs for regulatory safety assessment, Prof. Maurice Whelan (JRC, European Commission)
12:10 – 12:40
Talk 7: Standards relating to nanotechnology-based drug products in Japan, Dr. Kumiko Sakai-Kato
12:40 – 14:00
Lunch
Session 6: Emerging Nanomaterial Contaminants in FoodCo-Chairs: Dr. Yoko Hirabayashi, Mr. Neil Vary
Notetakers: Tan Yong Quan, Ivan Ng
Session 7: Generic Medical Products containing NanomaterialsCo-Chairs: Dr. Nadia Villar, Dr. Fanny Caputo
Notetakers: Herman Teo, Valerie Sin
14:00 – 14:10
Co-Chairs Remarks
Co-Chairs Remarks
20 min per item
14:10 – 14:40
Talk 1: Microplastics and Nanoplastics as an Emerging Food Contaminant: Gaps and Challenges. Dr. Calvin Yeo
Talk 1: ANMAT Regulatory pathway on Nanosimilarity: characterization strategies, comparability tests and specifications, Dr. Nadia Villar
Talk 5: Two decades of effort in developing best practices for genomics and its contribution to regulatory science, Leming Shi (Fudan University, Shanghai, China)
Panel Discussion and Q/A
Session 3: Innovative Application
Co-Chairs: Mr. Michael Renaudin (Swissmedic, Switzerland) and Prof. Lam Kwok Yan (Nanyang Technological University, Singapore)
14:40 – 15:10
Talk 2: A systematic approach to investigate microplastics hazards with specific consideration of the carrier hypothesis for polycyclic aromatic hydrocarbons (PAHs) Dr. Andrea Haase
Talk 2: European perspective on liposomal follow-on nanomedicinal products. Dr. Rene Thurmer
20 min per item
Talk 1: Tricia - Leveraging NLP to enhance risk assessment of incoming incident reports, Mr. Alexander Horst (Swissmedic, Switzerland)
15:10 – 15:40
Talk 3: Further facts from orally exposed nanomaterials. Dr. Kumiko Ogawa
Talk 3: The Harmonisation & Standardisation roadmap of the French metrology community for medicinal. Dr. Fanny Caputo
Talk 2: Medicrawl – Crawling online marketplaces for illegal products, Dr. Nicolas Perez Gonzalez (Swissmedic, Switzerland)
15:40 – 16:00
Coffee Break
15:20 – 15:40 Coffee Break
16:00 – 16:30
Talk 4: New developments in nanomaterial safety science for improved hazard assessment. Prof. Shareen Doak
Talk 4: Evaluation of nanomedicines. Dr Yasuhiro Abe
Talk 3: AI empowers the assessment for hepatotoxicity potential and clinical endpoints in drug development, Dr. Wenjun Bao (SAS, USA)
16:30 – 17:00
Talk 5: Guiding principles for the risk assessment of nanopesticides. Prof Melanie Kah
Talk 5: Matching the physi-chemical characterizations of nanostructures with their biomedical functions in vitro and in vivo. Dr. Xing-Jie Liang
Talk 4: Assessing allergenicity risk of proteins with AllerCatPro 2.0, Dr. Sebastian Maurer-Stroh, (Bioinformatics Institute, Agency for Science, Technology & Research, Singapore)
Panel Discussion and Q/A
Closing Remarks or Final Q&A (Discussion)
17:00 – 17:30
Talk 6: Finding the tiny plastic-needle in the haystack: how field flow fractionation can help to analyze nanoplastics in food. A/Prof. Katrin Loschner
Talk 6: Injectable Nanomedicines: Biopredictive Release Testing and IVIVC. A/Prof. Matthias Gerhard Wacker
All times are in Singapore Time Zone (GMT +8)
Day 3 ─ Friday, 21 October, 2022
Poster Display: 8:30 — 12:30, Location: Level 2, Rosewood Room & Nutmeg Room
Session 8: Nanotechnology in Agri-products and Feed
Co-Chairs: Dr. George Kass, Dr. Wannee Chinsirikul
Notetakers: Hui Yi, Patrick Gan
Session 9: Role of Nanotechnology in Precision Medicine
Co-Chairs: Dr. Luigi Calzolai, A/Prof. David Leong
Notetakers: Wang Yan Wen, Valerie Sin
Capacity Building Workshop
Co-Chairs: Dr Michael Johnston, Dr. Goncalo Gamboa
Notetakers: Yi Li, Zhi Ning
08:30 – 08:40
Co-Chairs Remarks
Co-Chairs Remarks
8:40 – 9:00
Talk 1: New EFSA guidances on nano risk-assessment - Implementation strategy in the area of feed additives. Dr. Orsolya Holczknecht
Talk 1: Regulatory challenges in development of Nanomedicine products. Dr. Amit K. Dinda
9:00 – 9:10
Introductions
9:10 – 9:40
Talk 2: Disruptive and Sustainable Technology for Agricultural Precision. Dr. Mervin Chunyi Ang
Talk 2: Continuous Manufacturing Platform for Nanoparticle-Based Therapeutics. Dr. Diane Burgess
30 min per item
An introduction to lipid nanoparticles (Dr. Michael Johnston, Health Canada)
9:40 – 10:05
Talk 3: Addressing Food Security at the Intersection of Digital and Drug Development Technologies. Prof. Dean Ho
Talk 3: Endothelial leakiness, a nanotoxic effect? A/Prof. David Leong
Considerations for the Quality, Safety, and Efficacy of Prophylactic Lipid Nanoparticle mRNA (Dr. Keith Peden, US FDA)
10:05 – 10:10
Q&A
10:10 – 10:20
Coffee Break
10:20 – 10:30
Coffee Break
10:30 – 10:40
Talk 4: Sustainable Approaches to Enhance Delivery of Nutrients and Agrichemicals for Maximizing Crop Yield. Prof. Ng Kee Woei
Talk 4: Safety assessment of nanomedicines- A snapshot of current practices and challenges. A/Prof. Ho Han Kiat
10:40 – 11:00
30 min per item
11:00 – 11:30
Talk 5: Indian landscape and achievements in the area of Nanotechnologies and products for Agriculture and food. Dr. Alok Adholeya
Talk 5: Taking Advantage of Disease Pathology for BBB transport: Development and Translation of Microglia -Targeted Systemic Dendrimer Nanomedicines. Dr. Kannan Rangaramanujam
Physicochemical characterization of lipid-based nanomedicines (Dr. Luigi Calzolai, Joint Research Center of the European Commission)
Lipid-Based Certified Reference Materials (Dr. Shan Zou, National Research Council Canada)
11:30 – 11:40
Talk 6: Application of advanced nanomaterials and nanostructured substrates
11:40 – 12:00
in In Vitro Diagnostics (IVD) and medical devices. Dr. Deanpen Japrung
Roundtable discussion
11:40 – 12:00
Talk 7: Translation of a Polymeric Nanomedicine: From Preclinical Data to Clinic Dr. Rana Sanyal
12:30 – 14:00
Lunch
Poster presenters to dismantle their posters
Session 10: Plenary Session on Safety Assessment & Closing Remarks
Co-Chairs: Dr George Kass, Ms Ligia Lindner Schreiner
Notetakers: Lian Jie, Wesley
14:00 – 14:10
Co-Chairs Remarks
14:10 – 14:40
Talk 1: Food for thought: Are we ready for new approach methodologies to assess nano-additives? A/Prof. Benjamin Smith
14:40 – 15:10
Talk 2: Advancing New Alternative Methods at The US Food and Drug Administration, Dr Suzanne Fitzpatrick
15:10 – 15:40
Talk 3: Biokinetics and biotransformation of nanomaterials in the body, Prof Cho Wan-seob
15:40 – 16:10
Talk 4: Exploring the use of New Approach Methodologies (NAMs) for the assessment of nanoscale considerations, Ms Maria Chiara Astuto
16:10 – 16:30
Coffee Break
16:30 – 16:40
Closing address by A/Prof. Joanne Chan
16:40 – 17:00
Closing Remarks by Dr. George Kass
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