COSMO CLINICAL RESEARCH
CCR is the first Clinical Research Organization in the Union Territory of Puducherry. Our facility is well connected with all modes of transport. As it is the first CRO in Puducherry, we have an early mover advantage with complete resource access.
CCR is a growing bioequivalence specialty organization providing end-to-end solutions for BA/BE studies for all dosage forms at an affordable cost.
CCR has a world class Clinical/Bioanalytical infrastructure located in Puducherry, India with a team of qualified and trained professional scientists.
MISSION
Cosmo Clinical Research focus is on disrupting the space of affordable research to the emerging markets with no compromise on quality and science.
To provide faster turnaround timelines for conventional healthy volunteer bioequivalence study and to offer academic research with industry standards.
Cosmo revolutionizes to ensure availability of quality generics in all geographies.
Our Strength
- Tailored approach to designing and conduct of bioequivalence.
- Quality system focused on continuous improvement.
- Integrity with great value and ethics.
Successfully Approved
- CDSCO (Central Drug Standard Control Organization)
Awaiting Regulatory Approvals
- ANVISA (The National Health Surveillance Agency)- Application submitted.
Targeted Regulatory Agency Approvals
- USFDA (United States Food and Drug Administration)
- WHO (World Health Organization)
- PICs (Pharmaceutical Inspection Co-operation Scheme)
CLINICAL
CCR is a GCP compliant DCGI ( Drug Controller General of India) approved facility managed by a team of about 30 researchers including 4 physicians.
- Clinical unit: 2
- Number of Beds : 60
- ICU unit – 1
- Number of Beds in ICU – 3
BIOANALYTICAL
State-of the-art Instrumentation with a team of qualified and experienced researchers with experience in method development, validation and sample bioanalysis per ICH M10.
- LC-MS/MS – 6 machines
- Number of Deep Freezers : 3 (ranging from -20ºC to -80ºC)
Cosmo provides cost effective solutions for clinical studies.
Bioanalytical Services
Clinical Trial Management
PK & Biostatistical services
Quality Assurance
Medical Writing
Regulatory Affairs
Auditing and Monitoring BE studies and clinical trials
Pharmacovigilance
Data Mangement Service
