About service
C&R Research provides comprehensive strategies and consulting services for global clinical trial development, through a number of professionals with extensive experience in multinational clinical trials in each country.
Global Regulatory Affairs Strategy
Global Feasibility Strategy
Budgeting
Market Access & Entrance Survey
CMC (Chemistry, Manufacturing and Controls)
CTD (Common Technical Document)
CDISC (Clinical Data Interchange Standards Consortium)
Global RA Expertise
C&R Research is able to manage real-time web based reporting from RA teams in the U.S., China, ASEAN countries, Japan and Taiwan. Then, Korea’s global RA consultants offer a range of database options and consulting to help clients establish regulatory strategies to suit multinational trials.
Feasibility & Budgeting
Through closer collaboration with its branch offices overseas, a global network of CROs and government-led clinical organizations, C&R Research acquires relevant data from each country to provide a streamlined global feasibility strategy per indication in each clinical development phase and a suitable study budget within a short period of time.
Global Market Survey
Based on the reports obtained from its branch offices overseas and partners, C&R Research selects a list of strategic countries suitable for multinational clinical trials and offer support in client’s development process in each country.
Global standardization
C&R Research provides regulatory compliance consulting on CMC, CTD and CDISC that are required in data submission for the U.S. Food and Drug Administration and European Medicines Agency.
For more information, Please click here.
For more information