BEIJING CANNY CONSULTING INC.

Globally GMP Compliance Conculting Services

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BeijingCANNYConsultingInc.

Dependable advisor on pharmaceutical regulations

25YEARS’

Professional consulting experience in the pharmaceutical industry

700+

GMP certification projects for China, EU, FDA, UK, Japan, Australia and WHO inspection

320+

Validation execution and guidance projects

2400+

Globally RA registration projects

1370+

Globally clients and pharmaceutical partners

30+

Experts from China, US and EU

Scope of Our Business

Dependable advisor on pharmaceutical regulations

GMP
Compliance Consulting

We provide GMP compliance services for various pharmaceutical companies in China, USA, EU, Australia, WHO and other countries/international organizations to ensure compliance with GMP regulations in relevant target markets.
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Verification Testing

Canny can provide validation compliance solution services covering the whole life cycle of pharmaceutical products to meet customers' needs in the same period/phase for validation-related system building/enhancement.
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MAH Services

Provide solutions covering the whole life cycle of MAH system
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Registration Services

Provides product registration, consulting services to global biotechnology and pharmaceutical companies.
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Pharma Information

Integrated platform for GMP-based total quality management design (B/S architecture)
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News

News 2023/02/21

PDA-TR90-CCS
News 2023/01/20

Technical Guide for the Elaboration of Monographs
Activities 2022/12/19

CPHI China 2023

19-21 June 2023 SNIEC, Shanghai, China

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Global Locations & Partners

Our consulting practice covers more than 20 countries and regions worldwide.

Shire
2
阿斯利康
4
5
诺和诺德
7
CSL
海美
10
11
12
13
15
IBSA
16
辉瑞
丽珠医药
信达
三叶草
天士力
民海
豪森
绿叶
扬子江
华润
甘李
新华
广济
人福
舒泰神

Investment retention for consultation and cooperation

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