-
Studies
of safety and tolerance.
- Individual and on population studies.
- Food effect studies.
|
-
Studies of bioavailability/bioequivalence.
- Studies of drugs interactions.
- Steady-sate studies. |
-
In Vivo/In Vitro and PK/PD correlations.
- Review of pre-clinical data and Toxicology
- Data management and Electronic Data Capture. |
-
Review and Development of ICH study protocols.
- Development and revision of CRF.
- ICH Integrated study report. |
| Pre-clinical
data review and Phase III Monitoring and Data Management. |
| Medication
administration: |
-
Oral administration.
- Pulmonary administration |
-
Routes
of administration via IM, IV, SC..
- Rectal and vaginal
administrations.
|
| Recruitment
of the study volunteers: |
|
By a
simple click, one knows the number of volunteers available
and eligible. We conduct one study at the time, the
volunteers are recruited quickly.
|
