Understanding Regulatory Framework for Chemical Products Registration in China

The webinar was successfully concluded on

December 10, 2024

Topics Covered:

Thank you for your interest in Freyr’s Webinar Series (FWS). The webinar ‘Understanding the Regulatory Framework for Chemical Products Registration in China’ was concluded on December 10, 2024. Here is an archived version for your perusal. 

Briefly, during the webinar, our presenters – Megha Barua and Yu Jing, discussed the following:

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

3. Post-Marketing Surveillance and Monitoring

  • Importance of post-marketing surveillance for chemical products
  • Adverse reaction monitoring and reporting

As a continuous practice, Freyr is destined to organize more webinar sessions related to Regulatory aspects of Life Sciences. We presume that you would like to be a part of all those sessions. If yes, let us have an opportunity to inform you about our next session.

   

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.

Host

Megha Barua

Speaker

Yu Jing