Company Name
Tigermed-Canny (Beijing) Consulting Inc.
Year of Establishment
2000
Annual Turnover(USD)
choose not to disclose
Company Introduction
Founded in 2000, BEIJING CANNY CONSULTING INC. is a consulting company focusing on regulatory compliance of drugs, health foods/dietary supplements, medical devices and functional cosmetics. Our providing services include marketing registration/application and GMP compliance in China and overseas, also the relevant strategic planning and the training. Now BEIJING CANNY CONSULTING, as a subsidiary of Hangzhou Tigermed Consulting Co, Ltd, has been a leading professional service provider in the industry of China.
For Your Attention, Scan the QRCode or Serch “china-canny 1998”
Main Competitive Advantages
N;
Website
http://www.china-canny.com
Other Competitive Advantages
1.Product Registration in China
Imported and domestic finished drugs, more than 40 cases
Imported and domestic APIs, more than 30 cases
Imported and domestic excipients, more than 10 cases
Imported packaging materials/containers, more than 5 cases
Health foods including imported, more than 30 cases
2. International drug registration
US ANDA/OTC/NDC, 6 cases
US-DMFs filed, more than 100 cases
EU MA application, 4 cases
COS/CEPs obtained, more than 50 cases
EDMF/ASMF filed, more than 60 cases
Australia ARTG, 5 cases
3.Plant Design & GMP Compliance
China and international GMP inspection, more than 200 successful cases including:
Small volume injection
Tyophilized powder for injection (including biologies, blood products)
Big volume injection
Solid dosage forms
Non-sterile API Sterile API
4.Training and Meeting Activities
Successfully held international meetings and training activities,
Together with both China and International regulatory authorities.
Milestone
Many 'First' We Made
China GMP compliance
FDA regulatory compliance
COS/CEP application
EU Feed FAMI-QS
Type III, IVDMF
Close FDA Warning Letter
Re-activating 'Suspended' COS/CEP
“Zero deficiency” passing FDA cGMP inspection
New Zealand GMP inspection
Sterile API FDA inspection
SFDA overseas inspection
Bio-product EU-GMP inspection ( phase II clinical trial)
……
Canny will, together with you, try to make more ' First' !