Pharma and biotech

 We conduct multinational clinical trials for pharma and biotech companies, as well as academic researchers, providing high-quality and cost-effective clinical trial management services. From start-to-finish, we have experience in designing and conducting Phase I to IV clinical trials and non-interventional studies (NIS) in compliance with ICH-GCP and other regulatory guidelines. We have successfully helped clients with drug development in a wide range of therapeutic areas e.g. cardiology, oncology, urology, CNS, endocrinology, HIV, gastroenterology, anaesthesia, and more. With our extensive experience, expertise, and continuously evolving service portfolio, we support our clients with either full-service solutions or specific components of their clinical trial projects, depending on their needs. 

 Our pharma and biotech CRO services include: 

• Clinical study start-up, including feasibility assessment and site evaluation, regulatory submissions, and preparation of the documentation
• Monitoring and site management
• Clinical project management
• Quality assurance and vendor management
• Pharmacovigilance/safety services
• Medical writing
• Data management and biostatistics
• Equipment rental services
• Outsourcing services when you need extra resources/interims solutions such as Clinical Project Managers (CPMs), Clinical Research Associates (CRAs), etc.