Tuesday, June 16, 2020

Explore the Latest Knowledge and Trends of Pharma Packaging Industry

A wide industrial experts' livestreams programme during Virturl Expo Connect are now avaialbe with more than 10 sessoions.
Conference Webcasts
 
Pharmaceutical Packaging and Drug Delivery Device Updates
18:15 ~ 22:00 18 June (UTC+8 China Time)
Organizer: InnoPack China, Pharmapack Europe
Co-organizer: DrugTimes

Sponsor: Du Pont China Holding., Ltd
Introduction: The conference webcast will invite speakers from multinational pharmaceutical and R&D companies, as well as consulting companies such as Baxter, PharmaSynergy, Tengroth Consulting and IQVIA to interpret the development trend of packaging technology and standards, share new thinking and successful experience in the industry, and comprehensively demonstrate the global development process of pharmaceutical packaging and drug delivery devices.
Agenda 
18 June (UTC+8 China Time)
18:15 ~ 19:00
Discussion on the Quality Attribute of Drug Package Materials under Bundling Review of Drug and Packaging
Ms. Luo Hong Yu
Principle scientist of Baxter Healthcare, R&D, China
19:00 ~ 19:30
Protective Pharmaceutical Packaging -  Overview of market trends – DuPont™ Tyvek® applications
DuPont Medical and Pharmaceutical Packaging
19:30 ~ 20:15
How to Improve the Safety of Drug Use Through Packaging
Dr. Cheryl Li
CEO & Co-founder, PharmaSynergy
20:15 ~ 20:45
Trends in Auto-Injectors and Pre-filled Syringes
Ms. Yasemin Karanis
IQVIA
20:45 ~ 21:30
Tips for Developing the Right Device for Your Injectable Drug Formulation and Bring to Commercialization Phase
Mr. Charbel Tengroth, Tengroth ConsultingContent
21:30 ~ 22:00
Q&A
Keynote Speakers
Luo Hong Yu
Principle Scientist of Baxter Healthcare, R&D, China
Yasemin Karanis
IQVIA
Charbel Tengroth
Tengroth Consulting
Dr. Cheryl Li
CEO & Co-founder,
PharmaSynergy
Yunxia Zhang Ph.D.
AP Application Development Specialist, DuPont Medical and Pharmaceutical Packaging
Diana Dai
Global Industry Vertical Manager, Pharmaceutical Packaging, DuPont Medical and Pharmaceutical Packaging
Sponsor
DuPont™ Tyvek® medical and pharmaceutical packaging provides the tear resistance, durability, breathability and superior microbial barrier to keep medical equipment and pharmaceuticals sterile throughout their lifecycle—protecting the health and well-being of millions. 
The CPhI & P-MEC China team look forward to meeting you online!

Monday, June 15, 2020

Learn about the latest trends in pharma deals

At Conference Webcast with Clarivate
View this E-mail online
Conference Webcast
2019 Deals Review & Deals in China


18 June 2020  14:30-15:15 UTC+8 China Time

Organizer: CPhI China 
 
Co-organizer: Clarivate
With the decrease ROI in R & D spending, pharmaceutical companies are trying to grab the market share with Licensing or M&A as much as they can. On the one hand, they become cautious and discerning in transactions; on the other hand, they spend a lot of money on high-quality assets. The market has more uncertainty in 2020 due to the impact of coronavirus. Still, it does not seem to prevent the life science people from moving forward, either to begin clinical trial rapidly or to speed up a large number of mergers and acquisitions. Ms. Tina Zhao, from Clarivate, will review the major deals with you in the pharmaceutical field in the past year and will review and comment on the deals of the Chinese market. We believe the 2019 Deals Review and Deals in China will support your business decisions in the future.
Keynote Speaker
Tina Zhao 
Life Sciences Solution Consultant, Clarivate


Tina Zhao has 13 years of experience in IP industry and life science industry. She joined Clarivate Analytics in 2015 as solution consultant for LS and IP products and services to support clients in the pharmaceutical industry for business development, market assessment, portfolio management, and IP risk management.  She graduated from National Taiwan University and has an M.S. degree in biochemistry and. She passed China Patent Attorney Bar Examination in 2014.

The conference is only 3 days away!
Register to acquire the latest trends for pharma deals! 
More Learning Opportunities
Date & Time
18 June 2020
18:15-22:00 UTC+8
19 June 2020
16:00-17:00 UTC+8
22 June 2020
16:00-17:00 UTC+8
23 June 2020
16:00-17:00 UTC+8
24 June 2020
16:00-17:00 UTC+8
Conference Title
Pharmaceutical Packaging and Drug Delivery Device Updates
 
Pharmaceutical Market in China: Policy Reform, Impacts and Opportunities
Best Practices in Pharmaceutical Remote Audits During COVID-19 and Beyond
How Indian API Register in China
 
Continuous Manufacturing of Drug Products Opportunities and Challenges
The CPhI & P-MEC China team look forward to meeting you online!

Tuesday, June 9, 2020

Explore the Latest Knowledge and Trends of Pharma Industry

A wide industrial experts' livestreams programme during Virturl Expo Connect are now avaialbe with more than 10 sessoions.
Conference Webcasts
A wide industrial experts' livestreams programme during Virtual Expo Connect are now available with more than 10 sessions.

This free-to-attend conference webcasts series features topics including pharma deals review in China, pharma market outlook and policy reform in China, Indian API registration in China, pharmaceutical remote audits, continuous manufacturing of drug and packaging & drug delivery solutions.

Register now to explore the latest knowledge and trends of pharma industry.
18 June 
14:30 ~ 15:15 
(UTC+8 China Time)
Tina Zhao
Life Sciences Solution Consultant, Clarivate
18 June 
18:15 ~ 22:00
(UTC+8 China Time)
2019 Deals Review and Deals in China
Introduction: With the decrease ROI in R & D spending, pharmaceutical companies are trying to grab the market share with Licensing or M&A as much as they can. On the one hand, they become cautious and discerning in transactions; on the other hand, they spend a lot of money on high-quality assets. The market has more uncertainty in 2020 due to the impact of coronavirus. Still, it does not seem to prevent the life science people from moving forward, either to begin clinical trial rapidly or to speed up a large number of mergers and acquisitions. Ms. Zhao Yuwei, from Clarivate, will review the major deals with you in the pharmaceutical field in the past year and will review and comment on the deals of the Chinese market. We believe the 2019 Deals Review and Deals in China will support your business decisions in the future.
Pharmaceutical Packaging and Drug Delivery Device Updates
Organizer: InnoPack China, Pharmapack Europe
Co-organizer: DrugTimes
Sponsor: Du Pont China Holding., Ltd
Introduction: The conference webcast will invite speakers from multinational pharmaceutical and R&D companies, as well as consulting companies such as Baxter, PharmaSynergy, Tengroth Consulting and IQVIA to interpret the development trend of packaging technology and standards, share new thinking and successful experience in the industry, and comprehensively demonstrate the global development process of pharmaceutical packaging and drug delivery devices.
Luo Hong Yu
Principle Scientist of Baxter Healthcare, R&D, China
Yasemin Karanis
IQVIA
Charbel Tengroth
Tengroth Consulting
Dr. Cheryl Li
CEO & Co-founder,
PharmaSynergy
Yunxia Zhang Ph.D.
AP Application Development Specialist, DuPont Medical and Pharmaceutical Packaging
Diana Dai
Global Industry Vertical Manager, Pharmaceutical Packaging, DuPont Medical and Pharmaceutical Packaging
19 June 
16:00 ~ 17:00
(UTC+8 China Time)
Dr. Annie Siu
(PhD, MBA), Principal Analyst, Pharma Intelligence | Informa
Pharmaceutical Market in China: Policy Reform, Impacts and Opportunities
Introduction: The policy reform is expected to reshape the pharmaceutical market in China. In this presentation, we shall discuss the followings, but not limited to:
    • The reform streamlines the clinical trials approval process in China, how would it affect the clinical trial landscape?
    • What kind of drugs would potentially get expedited review and approval in China?
    • What pricing and reimbursement strategies were taken by generics manufactures and innovative drug developers under the downward pricing pressure?
    • What are the incentives for innovation?
    • How to capture and analysis the opportunities for 505(b)(2) drugs, pediatric drugs, orphan drugs, drugs with breakthrough designation?
22 June
16:00 ~17:00 
(UTC +8 China Time)
Best Practices in Pharmaceutical Remote Audits During COVID-19 and Beyond
Jim Fries
CEO, RX360
Introduction: 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. 
    • Welome and Introduction
    • What is a Remote Audit?
    • Why Conduct a Remote Audit?
    • Best Practices
    • What is Next in the Remote Audit Arena? 
23 June 
16:00 ~ 17:00
(UTC+8 China Time)
Chengpei, Liu 
Registration Manager
China Chimopharma
How Indian API Register in China
"Drug Registration Management Approach" was newly revised after 13 years on 30 March 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. 
24 June 
16:00 ~ 17:00
(UTC+8 China Time)
Continuous Manufacturing of Drug Products Opportunities and Challenges
Dr. Deepak Hegde
Senior Vice President-CMC
EOC Pharma
Introduction: 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.
The CPhI & P-MEC China team look forward to meeting you online!