Pharma Clinical provides each client with tailored CRO services to deliver the most efficient clinical study. Our proven expertise and comprehensive services combined with our dedicated, experienced CRAs, enable us to deliver effective integrated planning and implementation. These services include:

• Phase I-IV clinical studies and medical surveys
• Worldwide project management
• Study design and protocol development
• CRF development
• Regulatory submissions
• Site selection
• Monitoring by experienced CRAs
• Data management and statistical evaluation*
• Central laboratory services*
• Quality management and audits
• Setting up of study related professional committees
• Pharmacovigilance services*, including narrative writing
• Clinical Study Report writing and publication support

* Provided through selected partners or external providers, Pharma Clinical delivers quality services in compliance with the ICH-GCP, EMA, FDA, local regulatory requirements and local law.