Booth No.5R-09
CategoryOutsourcing

WDB COCO Co., Ltd.

Booth No.:5R-09
Category:Outsourcing
Company Information
Email: Sales_g@wdbcoco.com TEL: +81-3-5144-2250 Address: 104-6127
TritonSquareY27F,1-8-11 Harumi,Chuo-ku,Tokyo JAPAN
URL: https://www.wdbcoco.com/
WDB COCO's philosophy is "to solve our customers' problems by guaranteeing the results of our work and providing new value, thereby contributing to the future of medicine." As an outsourcing partner (CRO) for our clients, the pharmaceutical and medical device companies, we provide comprehensive support for various post-marketing tasks, such as post-marketing surveillance and clinical research, with a focus on safety information management.

Company information

Address 104-6127
TritonSquareY27F,1-8-11 Harumi,Chuo-ku,Tokyo JAPAN
TEL +81-3-5144-2250
URL https://www.wdbcoco.com/
Email Sales_g@wdbcoco.com
Product introduction 【Pharmacovigilance】Foreign case safety information processing (post-marketing/clinical trial)
【Pharmacovigilance】Domestic case safety information processing (post-marketing/clinical trials)
【Pharmacovigilance】Literature evaluation work
【Pharmacovigilance】Support services related to safety measures information
【Pharmacovigilance】Support services for regular safety reports
【Post Marketing Surveillance】Facility contract and payment procedures
【Post Marketing Surveillance】Survey monitoring
【Post Marketing Surveillance】Case registration and data management
【Post Marketing Surveillance】Statistical analysis
【Post Marketing Surveillance】Medical information database research
【Clinical Trial/Regulatory Affairs/Quality Assurance】Pharmaceutical application document support
【Clinical Trial/Regulatory Affairs/Quality Assurance】Quality related document support
【Clinical Trial/Regulatory Affairs/Quality Assurance】Clinical development documentation support
【Clinical Research】Clinical Research Consulting
【Clinical Research】Research Administration
【Clinical Research】Data Management
【Clinical Research】Monitoring
【Clinical Research】Statistical analysis
【Clinical Research】Medical Writing
【Clinical Research】Audit,Due Diligence

Product introduction

【Pharmacovigilance】Foreign case safety information processing (post-marketing/clinical trial)【Pharmacovigilance】Domestic case safety information processing (post-marketing/clinical trials)【Pharmacovigilance】Literature evaluation work【Pharmacovigilance】Support services related to safety measures information【Pharmacovigilance】Support services for regular safety reports【Post Marketing Surveillance】Facility contract and payment procedures【Post Marketing Surveillance】Survey monitoring【Post Marketing Surveillance】Case registration and data management【Post Marketing Surveillance】Statistical analysis【Post Marketing Surveillance】Medical information database research【Clinical Trial/Regulatory Affairs/Quality Assurance】Pharmaceutical application document support【Clinical Trial/Regulatory Affairs/Quality Assurance】Quality related document support【Clinical Trial/Regulatory Affairs/Quality Assurance】Clinical development documentation support【Clinical Research】Clinical Research Consulting【Clinical Research】Research Administration【Clinical Research】Data Management【Clinical Research】Monitoring【Clinical Research】Statistical analysis【Clinical Research】Medical Writing【Clinical Research】Audit,Due Diligence