Phase I - IV (Clinical Trials: Interventional and Observational Studies)
PRU/APIC provides client driven services through its experienced team of clinical research professionals by operating throughout many regions.
Country feasibility, site and investigator selections are crucial steps for any clinical trials, as it impacts the study for its whole duration, our culture and policy competent experts can help you walk through the markets forecasts safely.
PRU/APIC consultants are experienced professionals with the knowledge to develop optimal trial designs and write protocols for clinical development programs. From phase I - IV we can address your data management and biostatistics needs and recommend the best solution for your study.
We support our clients at FDA meetings in Jordan, GCC and many other countries, in protocol discussions and in the presentation of the results of previous studies.
Support, consultation and facilitation to our clients during investigators meetings.
When a project is initiated a plan is put in place and our team manages its different aspects starting from focus groups all the way to vendors management, reporting and progress follow up.
Site Management and Clinical Monitoring
PRU/APIC provides the following monitoring services:
- Qualification visits
- Site initiation visits
- Interim monitoring visits
- Close out visits
- Site management
