Our Services
Site Identification, Selection & Feasibility
Identification and selection of the optimum sites, Key Investigators and Opinion Leaders are fundamental to the success of any clinical trial.
Metta’s Clinical Research expert’s have local knowledge and teams on the ground to facilitate close contact with investigators and sites. The existing relationships of our teams, with investigators and site staff, is fully leveraged during our feasibility process and throughout the study.
Strong and established relationships with experienced investigators help to facilitate a timely but comprehensive feasibility assessment to ensure the most appropriate and best recruiting sites chosen for our sponsor’s projects.
If you are planning to shorten your study timelines then the Metta’s Clinical Research targeted approach to Investigator recruitment, combined with our local experience, may be just what you need.
Patient Recruitment
It is a well-established fact that many clinical trials fail to meet their recruitment timelines. Delays in recruitment increase overall costs as the overall drug development timelines are pushed out with a negative impact on the product launch to market.
At Metta Clinical Research approach to ensuring accelerated patient recruitment and enhanced patient retention is multi-dimensional. The focus on patient recruitment and retention starts with the selection of the most appropriate sites where our structured feasibility indicates the best chance of recruiting the required patient population within the shortest time period.
In consultation with our sites and clients we utilize well defined processes and tools to accelerate patient recruitment e.g. recruitment projection calculator, site specific recruitment plans, patient outreach approaches, definition of patient flow and logistics etc.
Regulatory Services
Training
Metta Clinical Research offers customized training courses to the develop expertise necessary for effective clinical research. The training enables to master practical aspects of clinical trial conduct and management including a clinical trial, guideline, and ethical considerations.
- ICH-GCP TRAINING
- CLINICAL RESEARCH TRAINING
- PARTICULAR THERAPEUTIC AREA TRAINING
Other Services
- SOP DEVELOPMENT
- ARCHIVAL
- IP RETENTION
- PATHOLOGY AND RADIOLOGY SERVICES
- LOGISTICS
