Upcoming events

    • March 07, 2025
    • 8:00 AM
    • March 07, 2026
    • 8:00 PM

    CABS, a certifying organization of President’s Volunteer Service Award (PVSA)

    On March 7, 2025, Chinese American Bio/Pharmaceutical Society (CABS) was officially approved as a certifying organization empowered to confer the President’s Volunteer Service Award (PVSA). CABS will be responsible for verifying and certifying that volunteers have fulfilled the necessary requirements to qualify for the PVSA within a 12-month period.

    Any eligible adult or student volunteer who has contributed to CABS events will be required to self-track their hours on the service log sheet. The co-chairs of each committee will oversee the review and verification process. It is imperative that volunteers diligently maintain their hours tracking records as proof during potential audits. Please use the “PVSA Service Log” as a template.

    For any inquiries or clarifications, please reach out to O2 Chair: Liang He, PhD; heliangsu2018@gmail.com


    The President's Volunteer Service Award

    President's Volunteer Service Award - Wikipedia

    We are currently seeking sponsors to support this impactful event. If your organization is interested in partnering with us, please reach out via email at fundraising@cabsweb.org.


    • March 17, 2025
    • 12:00 AM
    • March 17, 2026
    • 11:59 PM

    Dear everyone,

    Greetings from the Chinese American Biopharmaceutical Society (CABS), Business and Career Development committee!

    Building upon the success of the CAN (Career Advisory Network) program last year, we have decided to launch the program again this year. We would like to extend a sincere invitation to you to join us as either a mentor or a mentee.

    The goal of CAN is to foster the development of future life sciences professionals and leaders through mentoring, skill enhancement, and networking platform, and also provide opportunities to give back to the community. The program runs for a period of six months and offers one-on-one mentoring sessions, as well as small and large group networking events. If you have any questions or concerns, please contact Feng Pan (fengpan.fox@gmail.com) or Jonathan Wong (jwong@enigmarecruiters.com).

    Program is scheduled to be formally launched on April 19 with a kick off meeting. Below is a tentative schedule:

          Mentor/Mentee registration opens: Monday, 3/17/2025

          Registration closes: Monday, 3/31/2025

          Program acceptance, notification emails sent: Monday, 4/7/2025

          Kick-off event: Saturday, 4/19/2025

          Mentoring groups convene: May to October

          Graduation: TBD

    Please visit http://www.cabsweb.org/can/ to learn more about CAN program. If you are interested in becoming a mentor or mentee, please complete the forms below.

          MENTOR registration:

    https://docs.google.com/forms/d/e/1FAIpQLSee9jAhkqnFaRMvI9l_ijafqBXsNFSj1X3a6ix6O5Au6Zhd8Q/viewform?usp=header 

          MENTEE application:

    https://docs.google.com/forms/d/e/1FAIpQLSfAq9pJM9wyVyGKsHtMf8kMsLuRRt-5bCXNpaSWLRJ6OBUb4Q/viewform?usp=header

    Please use the link or QR code above to register as a mentor or apply as a mentee.

    • April 28, 2025
    • 9:00 AM
    • April 28, 2026
    • 9:30 PM
    • 1633 Old Bayshore Hwy #280, Burlingame, CA 94010

    On April 26, 2025, the CABS Science and Technology Committee (STC) hosted the highly successful Clinical Development Workshop in Burlingame, CA, attracting over 80 attendees from the biotech and pharmaceutical community. This dynamic half-day event offered valuable insights into the clinical development, featuring industry experts from Genentech and ChemoCentryx/Amgen. Attendees engaged deeply with a comprehensive program covering study design, statistical considerations, clinical pharmacology, operational planning, and clinical trial protocol development, with enthusiastic participation throughout the day.

    The workshop opened with a warm introduction to CABS by its President, Dr. Kay Tong, followed by an overview of the agenda and speaker introductions by Dr. Liping Meng (Principal Scientist II, Gilead), Co-Chair of the STC.

    The first presentation featured Dr. Shichang Miao (Ex-VP, ChemoCentryx/Amgen), who delivered a comprehensive overview of clinical development fundamentals. Dr. Miao outlined the critical stages of drug development — from preclinical research to Phase 3 confirmatory studies, regulatory approval, and post-marketing surveillance. He also shared his personal 16-year journey leading the development of Tavneos, a small molecule drug, highlighting the many challenges and triumphs encountered before achieving FDA approval and the subsequent acquisition of ChemoCentryx by Amgen. His inspiring story deeply resonated with the audience, setting an encouraging tone for the day.

    Following that, Dr. Sara Glickstein Bar-Zeev (Principal Clinical Scientist, Genentech) presented "Foundations in Clinical Science and Study Design." She emphasized that clinical development is inherently long, costly, and high-risk, requiring careful strategic planning aligned with the desired product label. Dr. Glickstein explained the crucial role of the Clinical Development Plan (CDP) in guiding teams through iterative, learning-focused studies towards pivotal trials, and discussed the importance of rigorous clinical trial protocols to ensure study integrity and regulatory compliance. She also highlighted how artificial intelligence and large databases are increasingly shaping modern clinical development.

    Next, Dr. Chen Chen (Principal Statistical Scientist, Genentech) delivered an insightful presentation titled "Statistical Considerations in Clinical Trial Design and Analysis." Dr. Chen discussed the pivotal role of randomization in eliminating bias and ensuring statistical validity, as well as the strategic use of stratification to balance prognostic factors across treatment arms. He underscored the importance of careful endpoint selection, robust hypothesis testing, and proper sample size calculation. His discussion on the challenges posed by missing data, and the critical use of sensitivity analyses to ensure robustness, sparked lively and thoughtful audience engagement.

    After a brief break, Dr. Shichang Miao returned to deliver his second talk, "Clinical Pharmacology Studies." He emphasized that clinical pharmacology is a cornerstone of drug development, linking pharmacology, pharmacokinetics, toxicology, and clinical safety to guide dosing strategies and support regulatory submissions. Dr. Miao detailed key clinical pharmacology studies — including Food Effect, Drug-Drug Interaction, Mass Balance, and QTc evaluations — and addressed the unique considerations required for biologics versus small molecules. Attendees found this session particularly rich in practical insights and real-world examples.

    In the final talk, Dr. Sara Glickstein Bar-Zeev returned to present "Essential Elements of Clinical Trial Protocols." She outlined the critical components of a well-constructed protocol, including study rationale, objectives, design, safety and statistical methodologies, regulatory and ethical assurances, and data management policies. Dr. Glickstein emphasized that a poorly written protocol can result in added costs, delays, and challenges in data interpretation, and reinforced the fundamental importance of securing informed consent. Her detailed guidance provided attendees with a strong framework for effective protocol development.

    The workshop concluded with an engaging panel discussion and Q&A session led by Dr. Alex Yang (Senior Scientist, Vir Biotechnology), Co-Chair of STC. Panelists addressed a wide range of timely topics, including adaptive clinical trial designs, global regulatory variations, statistical considerations, and the impact of the FDA’s recent move to phase out mandatory of animal studies. The audience responded enthusiastically, raising numerous thoughtful questions and contributing valuable perspectives on the evolving clinical development landscape.

    The event concluded with loud applause and overwhelmingly positive feedback. The atmosphere remained vibrant as attendees enjoyed a networking lunch, fostering further discussions and new professional connections in a relaxed, collegial environment. Special thanks go to all the volunteers, whose dedication and hard work made this fully volunteer-supported event such a remarkable success. The 2025 CABS Clinical Development Workshop was a resounding success, leaving participants both inspired and better equipped to navigate the complex challenges of clinical development.

    This event was proudly sponsored by Sanyou Biopharmaceuticals Co., Ltd., whose generous support helped make this workshop possible.

    • September 13, 2025
    • 8:00 AM
    • March 09, 2026
    • 6:00 PM
    • South San Francisco Convention Center
    Register

    Welcome to 2025 BioPacific Conference  and thank you for sponsoring and exhibiting!

    This is Step 1. 

    To become a sponsor or exhibitor of 2025 CABS BioPacific Conference, please follow the steps below:

    1. Click the "Sponsor/Register" button at the right-corner and follow the step-by-step process to pay. The price will differ depends on level of sponsorship. Two payment methods:

    A. Pay by credit card.

    B. Pay by check. Click "invoice me" and then print out the invoice in your email. Mail the invoice together with the a check (payable to "CABS") to the following address: 268 Bush Street, #1888, San Francisco, CA 94104. U.S.A.

    2. You will receive an email to confirm your payment. High level sponsors will get free guest conference admission passes. Please go to Step 2 to register yourself and free guests for conference admission. 


    Any question? Please contact: fundraising@cabsweb.org  

    • January 01, 2026
    • May 15, 2026

    The Chinese American Biopharmaceutical Society (CABS) is pleased to announce the 2026 Data Science Summer Intern Program, a 10-week remote internship designed to train the next generation of data science leaders in the U.S. biopharma industry.

    Open to undergraduate, master’s, and Ph.D. students currently studying in the United States, this program offers hands-on experience applying AI, machine learning, and data analytics to real-world challenges across the drug development process — from target discovery to clinical research and commercialization.

    Interns will collaborate with data science teams from CABS member companies, attend professional workshops, and receive mentorship from industry experts.

      Timeline

    • Applications Open: January 1, 2025

    • Deadline: May 15, 2026

    • Internship Dates: June 15 – August 15, 2026

    This is a non-paid, remote, educational internship — CPT is not required.

      Contact Dr. Shicheng Guo (shicheng.guo@cabsweb.org) for more details.

      Registration Page: https://forms.gle/kfKVcw9N1ptJLaoj6



    • January 01, 2026

    Welcoming Liping Meng as President-Elect of CABS for 2026!

    Dear CABS Members, Partners, and Friends,

    It is with great pleasure that the Chinese American Biopharmaceutical Society (CABS) announce Liping Meng, PhD, Principal Scientist II at Gilead Sciences, as our President-Elect for 2026. With over 15 years of leadership experience in drug development and a longstanding commitment to CABS, Liping is well-prepared to guide the organization toward continued growth and innovation.

    Dr. Meng is a recognized scientific and CMC leader with a proven record of advancing therapeutics from preclinical development to commercialization. With a strong foundation in organic chemistry and broad expertise across analytical development, regulatory strategy, and quality control, she has successfully led more than 20 drug programs across all phases of development. Notably, she played a pivotal role in the regulatory journey of Sunlenca® (lenacapavir), leading to FDA approval as a groundbreaking, twice-yearly treatment for individuals with multidrug-resistant HIV. Before joining Gilead in 2015, Liping held a leadership position at AnaSpec. Prior to that, she conducted research at UC Davis after completing her doctoral degree in Organic Chemistry from the University of Tuebingen, Germany.

    Beyond her professional accomplishments, Liping has demonstrated exceptional leadership within CABS. Over the past decade, she has contributed significantly to the organization, serving as Co-Chair of the Membership Committee (2012–2017), Co-Chair of Business and Career Development Committee (2017-2023), and Co-Chair of Science and Technology Committee (2023–present).  Her outstanding contributions have been recognized with numerous accolades, including:

    ● 2014: CABS President’s Outstanding Service Award

    ● 2015: Outstanding Leadership and Service Award

    ● 2018: Distinguished Leadership and Contribution to CABS

    ● 2022: Ten Years of Extraordinary Leadership

    ● 2023: “Always There” Adamant Dedication Recognition

    ● 2024: Outstanding Co-Chair Award

    ● 2025: The USA President’s Volunteer Service Award

    Liping’s dedication to CABS and her remarkable professional journey make her an ideal leader for the next chapter of our organization. Her vision and expertise will ensure CABS continues to thrive as a hub for scientific excellence and global collaboration.

    With the election completed, Liping will now serve as the 2025-2026 President-Elect alongside Sihong Zhou, who will be the 2025-2026 President of CABS. Please join me in congratulating both Liping and Sihong on their new roles. We eagerly anticipate a dynamic tenure under their leadership and the continued growth of CABS through the collective efforts of our talented members and volunteers.

    Thank you for your continued support and dedication to CABS!

    Sincerely,

    Kay Tong,

    2024-2025 President of Chinese American Biopharmaceutical Society (CABS)




    • January 14, 2026
    • 8:30 AM - 3:00 PM
    • Morrison & Foerster LLP, 425 Market Street, San Francisco, CA 94105
    • 129
    Register

    CABS is a volunteer-based, non-profit organization headquartered in San Francisco, committed to advancing the life sciences and biotech industry through education, collaboration, and networking.

    The annual event, Investor Forum, held in conjunction with the JP Morgan Healthcare Conference, has been a hallmark of CABS for nearly 16 years. This year's forum is scheduled to take place on January 14th, 2026, from 8:30 am to 3:00 pm at Morrison Foerster’s San Francisco office (425 Market St, San Francisco, CA 94105).

    Our event will feature two insightful panel discussions—“Navigating Global Biotech Capital: Opportunities and Challenges in Cross-Border Investment” and “Investor–Entrepreneur Dialogue: Building the Next Generation of Global Biotech Leaders.” In addition, up to 10 early-stage companies will participate in the roadshow.

    Speakers Bio:

    Jonathan Norris  |  Managing Director, HSBC Innovation

    Jonathan Norris joined HSBC’s Innovation Banking Division in April 2023. He manages healthcare venture relationships and works with investors and companies on commercial banking and debt products.

    In addition, for more than a decade, Jonathan has written comprehensive reports on the venture healthcare ecosystem, covering venture fundraising, investment, valuations and exits. These reports have been widely cited in the ecosystem and he often speaks at major investor and industry conferences. He has more than 20 years of healthcare banking experience.

    Jonathan earned a B.S. in business administration from the University of California, Riverside, and a J.D. from Santa Clara University.

    Janet Xiao | Partner, Morrison & Foerster LLP

    Janet focuses her practice on worldwide patent procurement, patent portfolio management, and strategic planning for life sciences companies. Janet’s clients range from large multinational biopharmaceutical companies to emerging startup companies. Recognized as being highly sought after for patent prosecution and strategy mandates, Janet develops and strengthens her clients’ complex patent portfolios to maximize commercial value. She is instrumental in developing strategies for multibillion-dollar patent portfolios for pharmaceutical clients. She also works extensively in performing IP due diligence reviews in the contexts of VC investments, technology transactions, mergers and acquisitions, and marketing and manufacturing clearance for biopharmaceutical products.

    David Newman | Partner, Morrison & Foerster LLP

    David Newman serves as co-chair of the firm’s National Security and Crisis Management practices, drawing upon his deep experience in private practice and as a senior U.S. Department of Justice (DOJ) and White House official to represent clients in high stakes matters involving national security, geopolitical risk, emerging technology, and crisis management. David also leads the firm’s interdisciplinary Government Strategies group.

    A former Principal Deputy Assistant Attorney General for National Security (PDAAG) and Associate Deputy Attorney General, David advises companies navigating cybersecurity incidents, sanctions and export control enforcement, Committee on Foreign Investments in the United States (CFIUS) reviews, and Foreign Agents Registration Act (FARA) investigations. He has extensive experience conducting internal and government-facing cross-border investigations and representing clients in congressional inquiries and hearings.

    Qiang Lu |  Co-founder and Chairman of Board, GenFleet Therapeutics

    As GenFleet's Co-founder and Chairman of the Board, Dr. Qiang Lu oversees the company's strategic planning, financial management and business operations. With over 20 years of experience in life sciences research and the development of innovative therapies, Dr. Lu boasts extensive expertise across multiple sectors within the industry. Leveraging both practical approaches and strategic foresight, he has successfully advanced numerous products to pivotal clinical and commercial stages. Since its inception in 2017, GenFleet has built up industry-leading capabilities in developing novel drug candidates spanning small molecules and biologics and was publicly listed on the main board of Hong Kong Stock Exchange in September 2025. The company has set up a highly differentiated RAS-targeted matrix including selective and Pan RAS inhibitors of diverse molecular types, with most assets leading their categories in clinical progress in China or globally. In addition, the company has pioneered a series of first-in-class combination therapies based on dual-target synergistic mechanisms.

    Dr. Lu received his doctoral degree from Brandeis University and completed postdoctoral training at Tufts University. He joined Wyeth and Novartis in America and commanded numerous R&D programs to develop preclinical candidates. Following his overseas career, he served as vice president of WuXi AppTec in China, Chief Scientific Officer of Yangtze River Pharmaceutical Group and Gloria Pharmaceuticals, and senior vice president of CStone Pharmaceuticals. Besides spearheading many compounds into late-stage clinical trials, he also played a major role in operating and promoting multinational R&D platforms.

    Eric Hu | CBO, Expedition Therapeutics

    Eric Hu, Ph.D., serves as Chief Business Officer at Expedition Therapeutics, where he leads corporate strategy, business development, and partnerships, and supports fundraising and commercial initiatives. Prior to joining Expedition, Dr. Hu was Vice President of Corporate Development and Strategy and Head of U.S. Operations at Overland Pharmaceuticals, where he helped establish Overland Therapeutics and advance the company’s CAR-T programs. Before that, he was a senior member of the business development team at Turning Point Therapeutics prior to its $4.1 billion acquisition by Bristol Myers Squibb. Earlier in his career, Dr. Hu conducted research in antivirals, inflammation, and oncology before serving as an oncology search and evaluation liaison at Gilead Sciences. He earned his Ph.D. in Organic Chemistry from UCLA and his B.S. in Chemistry from Beijing Normal University.

    Leon Tang | Founder, InScienceWeTrust BioAdvisory

    Leon ‘Jun’ Tang, PhD is the founding partner of InScienceWeTrust BioAdvisory, a life sciences consulting company focused on the East-West cross-border BD&L and R&D collaborations in the pharmaceutical industry. ISWT BioAdvisory has advised 30+ biotech companies, investment funds, and other companies in the life sciences industry.

    Dr. Tang is also the founder of InScienceWeTrust Community, a US-based nonprofit that has more than 4,000 active members from the Asian biotech community. Dr. Tang serves as a scientific advisor to Mianus Capital, a boutique US-based healthcare PE/VC fund currently focused on ophthalmology. He is also an advisor to BioSpark, an Asian biotech professional’s association based in Massachusetts.

    Previously, Dr. Tang was a senior director of BD Search & Evaluation at Shanghai Henlius Biotech, a biotech sell-side analyst at Barclays Investment Bank, and a senior manager at the philanthropic venture fund of Cancer Research Institute of New York.

    Dr. Tang has published more than 50 academic papers in prestigious journals like Nature Reviews Drug Discovery, Lancet Oncology, Science Translational Medicine, Nature Communications, Science Advances, PNAS, etc.

    Dr. Tang received his bachelor’s degree from Tianjin University and master’s degree from Nankai University in China, a PhD degree from Icahn School of Medicine of Mount Sinai, and postdoctoral training at Memorial Sloan Kettering Cancer Center.

    Dr. Tang is well recognized expert in China biotech, and he was featured by Caixin Magazine, China Newsweek, Endpoints News, Fierce Pharma, and many leading investment banks.

    Wentao Zhang | Co-CEO, Frontage Laboratories, Inc.

    Hua Tu | President and CEO of Cerepeut

    Dr. Hua Tu is a scientist and biotech entrepreneur best known as the founder and former CEO of LakePharma, Inc., a leading U.S. biologics contract research, development, and manufacturing organization. He founded LakePharma in 2009 after more than 11 years at Tularik and Amgen, where he gained deep experience in biologics and drug development. Under his leadership, LakePharma expanded to six sites across California, Massachusetts, and Texas, serving hundreds of biopharmaceutical clients before being successfully acquired by Curia Global in 2021. Today, Dr. Tu serves as Chairman and CEO of the Maragin Health Foundation, a non-profit organization dedicated to advancing biomedical research. He is also President and CEO of Cerepeut, a leading longevity drug development company.

    Nan Ji | President and CEO of PAQ Therapeutics

    Dr. Nan Ji is President and CEO of PAQ Therapeutics. He is a prolific inventor and discoverer, with more than 30 patent applications filed. With three years spent at Kymera Therapeutics from the time the company was in its seed stage, he is also an expert at building an organization from the ground up. At Kymera, Dr Ji served as Vice President of Chemistry and played significant roles in driving the company scientific strategies, platform-building activities, and business development, as well as external collaborations crucial to the company’s success in targeted protein degradation technology. Before Kymera, Dr Ji spent 2 years at Mitobridge (now part of Astellas), where he was responsible for its NAD+-boosting portfolio with multiple approaches to modulate mitochondrial functions. Prior to that, he spent 7+ years at Novartis, where he contributed to and delivered multiple clinical and preclinical development candidates. Dr Ji earned his PhD in organic chemistry from Harvard University.

    Hu Li | Venture Partner, Eight Roads (ERVC)

    Dr. Hu Li is a Venture Partner of Eight Roads (ERVC). He manages existing portfolios, leads investment in therapeutics, participates in company creation including playing executive roles.

    Hu has over 25 years of multi-modality drug discovery, translational and preclinical development at strategic and operational levels within the global biopharmaceutical industry.

    Prior to ERVC, Hu was Vice President of Shanghai Miracogen, later acquired by Lepu Biopharma (2157.HK), a China biotech startup he cofounded. Hu was instrumental to the company’s R&D strategy, led pipeline construction, and advanced five ADC programs from discovery to the clinic, including one recent NMPA market approval, MRG003, three in registration trials including Claudin 18.2 ADC, CMG901, he co-invented and outlicensed to AZ for $1.1B USD.

    Before returning to China in 2015, Hu had 19-year tenure at GSK R&D in Philadelphia where he started as a bench biochemist and gained increasing responsibilities and significant experience in drug discovery in multiple TAs. From 2012 to 2014, Hu served as Discovery Biology Consultant for Scinovo providing drug discovery expertise for program evaluations for SR One and external alliances.

    Hu has B.Sc. in Chemistry from Nanjing University, M.Sc. from Chinese Academy of Sciences and Ph.D. in Biochemistry from Bryn Mawr College.



    • February 21, 2026
    • 12:00 PM - 4:00 PM
    • Sandpiper Community Center, 797 Redwood Shores Parkway, Redwood City, CA 94063
    Register

    You are cordially invited to attend 2026 Chinese New Year celebration party organized by the Chinese American Biopharmaceutical Society (CABS). Please come to enjoy music, singing, dancing,  and other entertainments performed by local Chinese dancers and artists, experience authentic Chinese foods, having fun solving riddles, prize draw and much more.

    Please mark your calendar for this free event, and please note:

    1, If you want to have lunch onsite, you have to make a donation to get a ticket for lunch. No ticket no lunch and no onsite donation accept.

    2, Without a lunch ticket, you are welcome to register free ticket to enjoy our free show, it's a must as there is a max capacity limit of activity center.

    3, Kids under 5 years old do not need a donation to get a lunch ticket.

    4, Your early online donation will be greatly appreciated.

    We look forward to seeing you there and celebrating Year of the Horse together!







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