Clinical Trial Services
Phase I to IV clinical trials in compliance with ICH/GCP guidelines and local regulations :
- Feasibility studies
- Site selection and study start up
- Ethics Committee submission, file preparation and tracking procedures
- Investigator selection and training
- Site management (pre-study site visits, initiation, monitoring and close-out)
- Serious Adverse Event (SAE) form checking and reporting
- ICH/ GCP training
- Biological sample logistics
Pharmacovigilance
- Post-marketing surveillance
- Periodic Safety Update Report (PSUR) compilation
Pharmaceutical Services
- Pharmaceutical Drug Registration
- Product Representation, Marketing and Sales
- Market research : drugs and medical devices
- Multi -Country solutions
Additional Services
We provide the following services with partners:
- Data Management
- Epidemiologic studies
- Pharmacoeconomic studies
- Consumer awareness programs
Clinical Trial Services
Phase I to IV clinical trials in compliance with ICH/GCP guidelines and local regulations :
- Feasibility studies
- Site selection and study start up
- Ethics Committee submission, file preparation and tracking procedures
- Investigator selection and training
- Site management (pre-study site visits, initiation, monitoring and close-out)
- Serious Adverse Event (SAE) form checking and reporting
- ICH/ GCP training
- Biological sample logistics
Pharmacovigilance
- Post-marketing surveillance
- Periodic Safety Update Report (PSUR) compilation
Pharmaceutical Services
- Pharmaceutical Drug Registration
- Product Representation, Marketing and Sales
- Market research : drugs and medical devices
- Multi -Country solutions
Additional Services
We provide the following services with partners:
- Data Management
- Epidemiologic studies
- Pharmacoeconomic studies
- Consumer awareness programs