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Exhibitor Webinar

Popular Suppliers Sneak Peek

  • 15:30~15:50 18 June (UTC+8)

    CREADY-Guarantee of registration and clinical trial for imported drug license based on comprehensive lab

    Wang Xinxin

    Shijiazhuang CREADY Pharmaceutical R&D Inc.


  • 09:00~09:20 19 June (UTC+8)

    Lachance Group, leading manufacturer of bile acids -An innovative product on protecting liver and gut health

    Fred Xu

    Shandong Longchang Animal Health Product Co. ,Ltd


  • 14:30~14:50 19 June (UTC+8)

    Heron Pharma - the Leading Supplier of Full Vitamin D Derivatives

    Simon Zi

    Heron (Shanghai) Pharmaceutical Sci & Tech Co., Ltd.


  • 15:30~15:50 19 June (UTC+8)

    1.Recombinant Human Epidermal Growth Factor 2.Recombinant Human Long Arg3-like Growth Factor-1

    Yongbo Yu

    Jilin Province Foen Biological Co., Ltd.


  • 16:00~16:20 19 June (UTC+8)

    Application of Yeast Nutrients on Bio-pharmaceutical industry

    Woodrow Xiong

    Angel Yeast Co.,Ltd.


  • 09:30~09:50 20 June (UTC+8)

    green veterinary drugs, service to global animals

    Polly Du

    Hebei Huarun Pharmacy Co., Ltd.


  • 13:00~13:20 23 June (UTC+8)

    The introduction of Bloomage Biotech and its product

    Li Dejie



  • 13:30~13:50 23 June (UTC+8)

    Choline, The ingredient we may have ignored!

    Isabella Zhao



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Conference Webcasts

A Wide Industrial Experts' Livestreams Programme

Best Practices in Pharmaceutical Remote Audits During COVID-19 and Beyond

This presentation will discuss the role that remote auditing has played in pharmaceutical quality during the coronavirus pandemic. It will discuss best practices, and observations from both the supplier and manufacturer point of view. The presentation will also cover the expected role that remote auditing will continue to play post COVID-19.

Language: English


How Indian API Register in China

"Drug Registration Management Approach" was newly revised after 13 years on March 30, 2020 to encourage innovation and optimize and improve the efficiency of the drug review. It introduced the new concept and system, updated the registration management, established a link between the review and approval system, and strengthened the concept of whole life cycle of drug management. Our company has been the exclusive agency of more than 80 international API suppliers and collaborated with over 700 domestic production enterprises. Referring to our business model and registration experience, the speech will focus on an overview of the registration and administration of imported APIs, related judicial institutions and laws and regulations, and declaration requirements and review process so as to together explore coping strategies and future industry trends.

Language: English


Continuous Manufacturing of Drug Products Opportunities and Challenges

One of the innovations in the field of pharmaceutical manufacturing has been continuous manufacturing. The talk will outline the concept, features, potential benefits and control strategies used for continuous manufacturing. Quality/ GMP considerations for implementing continuous manufacturing in the small molecules space along with a key factor- how to bridge existing batch manufacturing with continuous manufacturing, would be addressed. Regulatory and Quality Considerations including a summary of current regulatory environment, relevant regulations and guidelines including industry stand on current guidances would be discussed. Quality/GMP Considerations and Post-approval implementation would also be explored in the talk.

Language: English


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