Founded in April 2021, Beijing Cowaymed Consulting is a Beijing-based consultancy focusing on regulatory compliance of drugs and other health products at home and abroad. Cowaymed provides consulting services including Regulatory affairs consultation for drugs, GMP compliance consultation for drugs and medical devices, Product launching & technology transfer, Marketing authorization holder consultation and Pharmaceutical translation.
The senior consultants of Cowaymed have more than 10 years of experience working in well-known consulting companies and pharmaceutical companies. They have professional skills and a strong knowledge of RA and GMP. With years of experience in RA and GMP compliance, Cowaymed has established a solid cooperation with authorities and field experts.
Our values of honesty and cooperation enable us to develop more business and cooperation. On the basis of win-win principle and mutual development, Cowaymed is presenting more mature and efficient services to help our customers seize opportunities and predict market performance.
Year of Establishment:
2017
Total Assets(USD):
less than 500,000
Total Number of Staff:
10-50
Main Competitive Advantages:
Brand Name,International Approvals/Standards,Experienced R&D Staff,Small Orders Accepted,Reputation,Quality Service
Other Competitive Advantages:
1. Rich experience of multiple types of projects and be able to predict potential difficulties.
2. Full-time staff, professional experience and operation.
3. Strong supports from more than 30 domestic and international experts.
4. Strong supports from strategy partners worldwide.
5. Covering the creation of R&D system, guidance for R&D, Registration, clinical trials, GMP compliance support
Patents and Copyrights:
Business Type:
Agent,Service Provider
R&D capacity:
Own Brand
Annual Turnover(USD):
500,000 to 99,999,999
Main Sales Markets:
North America,Western Europe,Eastern Europe,Australasia,Asia
Other Competitive Advantages:
1. Rich experience of multiple types of projects and be able to predict potential difficulties.
2. Full-time staff, professional experience and operation.
3. Strong supports from more than 30 domestic and international experts.
4. Strong supports from strategy partners worldwide.
5. Covering the creation of R&D system, guidance for R&D, Registration, clinical trials, GMP compliance support
Patents and Copyrights:
Audited Supplier
Pharma Sources Insight JANUARY 2024
