Understanding Regulatory Framework for Chemical Products Registration in China
December 10, 2024
45 Minutes
Join the Webinar at your Convenient Time
For AMR & EU
10:00 EST | 9:00 CST | 11:00 BRT | 16:00 CET
For RoW
18:00 AEDT | 10:00 MSK | 15:00 MYT | 12:30 IST
What is it all about?
This webinar offers a comprehensive overview of China’s regulatory landscape for chemical products. We will delve into the roles of key regulatory bodies, including the NMPA, SAMR, and GACC, and discuss the compliance requirements for product safety and standards management.
Attendees will gain valuable insights into the steps necessary for successful registration and market entry in China. This session is essential for global brand owners, manufacturers, distributors, and importers of chemical substances looking to navigate the complexities of regulatory compliance.
We look forward to your participation!
The webinar will be hosted by Megha Barua and Yu Jing, and during this session, our experts will discuss:
1.Introduction to Chemical Products Registration in China
- Overview of China’s regulatory landscape
- Key regulatory bodies: NMPA, SAMR, and GACC
- Importance of compliance for product safety and standards management
- Steps for successful registration and market entry
2. Regulatory Requirements and Processes
- Compliance requirements for chemical products
- Best practices for product safety assessment and registration
- Challenges and strategies for navigating the registration process
Post-Marketing Surveillance and Monitoring
- Importance of post-marketing surveillance for chemical products
- Adverse reaction monitoring and reporting
Given these important topics, we understand your busy schedule and hope you can join us for this informative session on December 10, 2024.
Register now to stay informed and ensure compliance with Chemical Products Registration in China!
Megha Baruah is the Delivery Owner, handling the Consumer Division projects for Freyr’s Cosmetics, Food, and Chemicals Centre of Excellence (CoE). She mostly oversees the requirements and projects of the AMR and EU regions. Megha comes from a biotechnology background and has four (04)+ years of experience in the Healthcare and Regulatory industry. She liaises between cross-functional teams in the organization to complete various projects, thereby keeping up with clients’ expectations and handling all tasks and schedules that lead to overall profitability.
Yu Jing has over 10 years of experience in Regulatory Affairs for consumer products, specializing in raw materials and product safety assessment, product efficacy evaluation, and compliance review. She handles submissions for cosmetics, foods, disinfection products, hygiene products, and household cleaning items, conducting gap analyses and reviewing applications to health authorities. Her expertise also includes regulatory intelligence collection, strategy establishment, post-marketing surveillance, and adverse reaction monitoring. Holding a Master of Medicine with research in drug toxicology, Yu Jing is an active member of the Chinese Toxicology Society, demonstrating her commitment to safety and compliance in the industry.