In the evolving landscape of healthcare and medicine, the journey from innovative research to patient-ready treatments is complex and fraught with challenges. At Baupharma, we are dedicated to making this journey smoother, faster, and more efficient. From early-stage development to post-marketing surveillance, our team of experts provides end-to-end support across all phases of clinical research.

Our range of clinical research services includes:

● Project Management
● Feasibility and Site Selection
● Start-up
● Recruitment
● Site Management
● IP Management

● Protocol development
● Manuscript development
● Clinical Study Report ICH E3
● Advisory Board Support
● SAS and SPSS
● Tables, Listing and Figures

● CRF Development: paper or EDC
● Database set-up within
   o Oracle Clinical for paper-CRF
   o ORDC and Viedoc for e-CRF
● In-stream Data Cleaning
● External data transfers
● CDISC & Coding
● Query process metrics, and data reporting
● AE/SAE reconciliation and reporting
● Database lock

● CRA In/Out-sourcing
   o Full-time
   o Part-time
● Clinical Trials Assistant
● Study Coordinator
● Accredited GCP training programs for site and sponsor staff ¨

● Clinical Trial Applications
● Safety reporting
● IP logistics (import and export licenses) Central lab logistics

● Local expertise with regulatory procedures of each country
● Strong network with key regulators of clinical trials
● Extensive up-to-date knowledge of regulations
● Constant mapping of regulatory procedures and updates
● Understanding of challenges and expertise in handling delays

Ready to Elevate Your Clinical Research? Discover the Baupharma difference. Contact us today to learn how our expert team, comprehensive services, and commitment to excellence can bring your clinical research projects to new heights.