Metta Clinical Research
Site management organization (SMO) providing clinical trial site services including site identification and feasibility, patient recruitment, regulatory submission support to ethics committees, placement of study coordinators and site management associates, and customized training. Operates from Nagpur, India and supports multiple therapeutic areas.
Industries
Nr. of Employees
small (1-50)
Metta Clinical Research
Products
Site Identification, Selection & Feasibility
Identification and selection of optimum sites, Key Investigators, and Opinion Leaders for clinical trials using local knowledge and established relationships.
Clinical Research Coordinator and Site Management Associate Services
Metta Clinical Research provides highly qualified and experienced study Coordinators (SCs) and Site Management Associates (SMAs) to help and support both principal investigators and sponsors, assisting with daily clinical trial activity and high patient recruitment.
Patient Recruitment
Multi-dimensional approach to ensuring accelerated patient recruitment and enhanced patient retention in clinical trials.
ARCHIVAL
Document archival services for clinical trials.
IP RETENTION
Investigational product retention and management services.
ICH-GCP TRAINING
Customized training courses to develop expertise necessary for effective clinical research and master practical aspects of clinical trial conduct.
Site Identification, Selection & Feasibility
Identification and selection of optimum sites, Key Investigators, and Opinion Leaders for clinical trials using local knowledge and established relationships.
Clinical Research Coordinator and Site Management Associate Services
Metta Clinical Research provides highly qualified and experienced study Coordinators (SCs) and Site Management Associates (SMAs) to help and support both principal investigators and sponsors, assisting with daily clinical trial activity and high patient recruitment.
Patient Recruitment
Multi-dimensional approach to ensuring accelerated patient recruitment and enhanced patient retention in clinical trials.
ARCHIVAL
Document archival services for clinical trials.
IP RETENTION
Investigational product retention and management services.
ICH-GCP TRAINING
Customized training courses to develop expertise necessary for effective clinical research and master practical aspects of clinical trial conduct.
Services
Identification and selection of sites and investigators plus feasibility assessment to align sites with study protocol requirements.
Execution of patient recruitment activities and strategies to support enrollment timelines.
Preparation and submission of regulatory and ethics documentation to obtain approvals for clinical trials.
Customized training courses and workshops on practical clinical research topics and Good Clinical Practice (GCP).
Supply and placement of trained study coordinators (SCs) and site management associates (SMAs) to support daily trial activities.
Online registration form and onboarding for investigators wishing to join the company's network.
Identification and selection of sites and investigators plus feasibility assessment to align sites with study protocol requirements.
Execution of patient recruitment activities and strategies to support enrollment timelines.
Preparation and submission of regulatory and ethics documentation to obtain approvals for clinical trials.
Customized training courses and workshops on practical clinical research topics and Good Clinical Practice (GCP).
Supply and placement of trained study coordinators (SCs) and site management associates (SMAs) to support daily trial activities.
Online registration form and onboarding for investigators wishing to join the company's network.
Expertise Areas
- Clinical trial site management
- Patient recruitment and enrollment
- Regulatory and ethics committee submissions
- Clinical staff training and GCP
Key Technologies
- Clinical trial site management
- Site feasibility assessment methodologies
- Patient recruitment methodologies
- Ethics committee submission preparation
News & Updates
A one-day workshop held at N. K. P. Salve Institute of Medical Sciences & Research Centre and Lata Mangeshkar Hospital, Nagpur covering Good Clinical Practices with speakers from industry.
A one-day workshop held at N. K. P. Salve Institute of Medical Sciences & Research Centre and Lata Mangeshkar Hospital, Nagpur covering Good Clinical Practices with speakers from industry.