Presented by
Management Forum
Registration of Veterinary Pharmaceuticals in China Training Course
Learn how to navigate the regulatory system of veterinary pharmaceuticals in China.
16 October 2024
+ 27 February 2025, 26 June 2025, 23 October 2025 »
from £150
- Format: Live online
- CPD: 1.5 hours for your records
- Certificate of completion
- Veterinary Pharmaceutical Submissions in the EU
- A Practical Approach to Veterinary Vaccine Development and Registration in the EU
- The Animal Health Summer School: Working Through Veterinary Drug Development in the EU and USA
- Practical Implementation of GCP in Veterinary Field Studies
- A Practical Approach to Developing the CMC Package for Veterinary Pharmaceutical Products
- Registration of Veterinary Pharmaceuticals in China
- Animal Feed and Feed Additive Registration in China and Thailand
Course overview
The market demand for veterinary drugs in China is substantial. However, companies must navigate the regulatory barrier due to China’s distinct and separate regulatory system.
This course aims to provide practical advice and guidance on successfully obtaining market approval for veterinary drugs in China. Participants will gain a comprehensive understanding of the necessary requirements.
Throughout the programme, expert speakers will elucidate relevant regulations, and registration procedures through presentations, while also addressing participant questions.
This course is part of our Regulatory Affairs Training course collection, which features updates on the latest regulations to registration procedures and strategies.
Benefits of attending
- Understand the relevant regulatory systems and frameworks
- Gain an insight into the specific data requirements
- Explore registration processes
- Learn the associated testing requirements
- Consider the costs for obtaining market approval
- Confirm about the applicability of overseas registration files and common issues encountered during import registration
Who should attend
This event will be beneficial to companies interested in expanding into the Chinese markets, as well as to registration personnel responsible for market approval matters:
- New entrants to registration departments
- Veterinary medicinal product manufacturers
- Registration managers
- Research and development departments
- Academics with an interest in commercialising opportunities
You may also be interested in our Animal Feed and Feed Additive Registration in China and Thailand course running on the same day!
This course will cover:
China market access and regulatory requirements for veterinary drugs (VD)
Regulatory framework
- Competent authorities and responsibilities
- Definition of veterinary drugs (VD) in China
- Overview of regulations
Registration of imported feed/feed additives in China
- Registration types
- Data requirements
- Registration process
- Timeline
- Requirements for testing in China (e.g., confirmatory clinical trials)
- Validity period of registration
- Other key points (commissioned production, Good Manufacturing Practice (GMP), Chinese veterinary pharmacopoeia and other import legal standards, test guidance)
Bi Jun
knoell
Bi Jun is a pharmaceutical expert with more than 10 years of experience in health product development and registration in China. Currently in Knoell Shanghai, he is mainly responsible for regulatory support and the registration of pharmaceutical ingredients and packaging materials for human drugs (DMF), Biocides, feed/feed additives and veterinary drugs.
NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:
- 30% off the 2nd delegate*
- 40% off the 3rd delegate*
- 50% off the 4th delegate*
Please contact us for pricing if you are interested in booking 5 or more delegates
16 October 2024
Live online
11:45-13:15 UK (London) (UTC+01)
12:45-14:15 Paris (UTC+02)
06:45-08:15 New York (UTC-04)
Course code 15169
- GBP 175
- EUR 255
- USD 289
- 1.5 hours of live online training
- Browser-based, no download usually required
- See presenters and interact with fellow attendees
- Download documentation and certification of completion
- Fair transfer and cancellation policy
Not ready to book yet?
for 7 days, no obligation
27 February 2025
Live online
11:45-13:15 UK (London) (UTC+00)
12:45-14:15 Paris (UTC+01)
06:45-08:15 New York (UTC-05)
Course code 15170
- GBP 150 175
- EUR 220 255
- USD 250 289
Until 23 Jan
- 1.5 hours of live online training
- Browser-based, no download usually required
- See presenters and interact with fellow attendees
- Download documentation and certification of completion
- Fair transfer and cancellation policy
Not ready to book yet?
for 7 days, no obligation
26 June 2025
Live online
11:45-13:15 UK (London) (UTC+01)
12:45-14:15 Paris (UTC+02)
06:45-08:15 New York (UTC-04)
Course code 15256
- GBP 150 175
- EUR 220 255
- USD 250 289
Until 22 May
- 1.5 hours of live online training
- Browser-based, no download usually required
- See presenters and interact with fellow attendees
- Download documentation and certification of completion
- Fair transfer and cancellation policy
Not ready to book yet?
for 7 days, no obligation
23 October 2025
Live online
11:45-13:15 UK (London) (UTC+01)
12:45-14:15 Paris (UTC+02)
06:45-08:15 New York (UTC-04)
Course code 15257
- GBP 150 175
- EUR 220 255
- USD 250 289
Until 18 Sep
- 1.5 hours of live online training
- Browser-based, no download usually required
- See presenters and interact with fellow attendees
- Download documentation and certification of completion
- Fair transfer and cancellation policy
Not ready to book yet?
for 7 days, no obligation
* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price; and apply only when booking multiple delegates on the same date.
Finland
- Orion Corporation
- Orion Corporation Orion Pharma
