The Current and growing complexity of the clinical studies requires to have methods and standardized processes to conduct efficiently the different activities and responsibilities which this activity demands.
Sponsors and CROs can centralize the main activities of different clinical research sites in Global Medical Logistics to ensure centralized and integral study management.
Likewise investigators and research sites can be supported on the experience and procedures of Global Medical Logistics.
Answer to feasibilities
With a broad knowledge in feasibility process of clinical studies, the documentation and quality information that must be submitted, we can support you to answer appropriately with certainty feasibility questionnaires for clinical studies.
Training
With qualified staff certified in Good clinical practices and specialists in different areas, we can offer courses and training in different areas:
GCP
Ethics/Bioethics
Methodology of the investigation
Local and international regulations
Regulatory support
Thanks to the knowledge in local regulations of our staff , we can support you in the preparation and presentation of the regulatory documents to applicable regulatory entities, Ethics Committees and Health authorities.
Handling of product of investigation
We have the experience and capacity to support research sites / principal investigators for the adequate handling of the product of investigation and clinical equipment in the different processes:
