Hangzhou Tigermed Consulting Co LtdHangzhou Tigermed Consulting Co Ltd - ESG Rating & Company Profile powered by AI

Industry Group:Pharmaceuticals

If you work at Hangzhou Tigermed Consulting Co Ltd and you would like to licence your Sustainability rating, please contact us. This ESG rating includes 17 UN SDGs including: 'Gender Equality', 'Reduced Inequalities' and 'Partnerships for the Goals'. The webpage is a zero-cost Sustainability assessment for Hangzhou Tigermed Consulting Co Ltd.

Hangzhou Tigermed Consulting Co Ltd in the Pharmaceuticals industry gained a UN SDG ESG Transparency Score of 0.9; made up of an environmental score of 0.0, social score of 0.0 and governance score of 2.7.

SDG Transparency Score for Hangzhou Tigermed Consulting Co Ltd 

0.9

Low Impact
0 - 3
Medium
4 - 6
High
7 - 10
Last Score Update: 2023-07-01
What drives the score for Hangzhou Tigermed Consulting Co Ltd 
0.0

Environmental

0.0

Social

2.7

Governance

Detailed ESG Breakdown
SEVVA Platform offers unique drill down to the underlying sources powering the ratings. Break down your ESG analysis by 17 UN SDGs and 8 additional governance factors.

Peer Group Comparison

RankCompanySDG Transparency Score Performance
1Novartis AG
9.2
High
2Daiichi Sankyo Co Ltd
8.9
High
.........
2549Zhejiang Wecome Pharmaceutical Co Ltd
1.0
Low
2549Zhejiang Yatai Pharmaceutical Co Ltd
1.0
Low
2585Hangzhou Tigermed Consulting Co Ltd
0.9
Low
2585Agimexpharm Pharmaceutical JSC
0.9
Low
2585Alexza Pharmaceuticals Inc
0.9
Low
2749Xynomic Pharmaceuticals Holdings Inc
0.0
Low
2749Zyden Gentec Ltd
0.0
Low
.........
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Peer Companies Benchmark
SEVVA Platform benchmarks each company against a peer group. View the full score distribution for peers by logging into SEVVA

Frequently Asked Questions

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Potential Risks for Hangzhou Tigermed Consulting Co Ltd
These potential risks are based on the size, segment and geographies of the company.

Hangzhou Tigermed Consulting Co., Ltd. provides contract research organization services in China and internationally. It operates through Clinical Trial Solutions; and Clinical-Related and Laboratory Services. The company offers regulatory submission and approval, medical translation, and good manufacturing practice (GMP) consulting; clinical services in the areas of medical science, early clinical and late phase development, medical monitoring, project management, patient recruitment, and quality management system; and biometrics services covering data management, biostatistics, and statistical programming. It also provides integrated technology services, such as site management, pharmacovigilance, third party audit and training, medical imaging, clinical trial system solution, central laboratory, pre-clinical, and research hospital; medical device/ in vitro diagnostics (IVD) services comprising medical device testing, regulatory submission, clinical evaluation and trials, GMP certificate, EU MDR and IVDR preparation, and value added services; and post-marketing study, real world evidence, and vaccine clinical trial services. The company was incorporated in 2004 and is headquartered in Hangzhou, China.

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