PDC provides regulatory consulting either as a customized stand-alone service or through our full-service clinical trials. Our regulatory experts have years of experiences with the SFDA, DOH, DHA, FDA, MoH and other national and international health authorities in the region and are familiar with differences in local regulatory requirements. Our experts can provide you with feasible strategies to ensures rapid achievement of tasks towards faster start up, closure and in compliance with applicable guidelines in KSA, UAE, GCC and over MEA region.
- Registration with submissions to the health Authorities (IRB/IEC & MoH)
- Laising with sites and investigators
- Providing Insurance Certificates
- Providing Medical Translation Services
- Regulatory Assessments
- Importing and Exporting Licenses