Drawing upon our 30 years of expertise,
we are honored to facilitate the seamless
execution of your clinical trials
- Product development studies
- Selection and supply of reference products and/or test products
- Generation of study protocols and documentation for Bioethics
- Pharmacovigilance and safety monitoring service
- Post-authorization safety studies
- Import/export and supply of Investigational Medicinal Products (IMP) and Medicines for Clinical trials from non-EU countries