Arandi Development - Safe development of better medical products
 

 

  Our services    
     
       
 

Medical monitor

We provide around-the-clock medical support for CRAs and study sites. Patient eligibility, protocol issues and patient safety questions can be resolved with minimum delay. Our MDs may also serve as liaisons with regulatory authorities and ethics committees.

Safety physicians available 24/7

An EU-based safety physician to support pharmacovigilance activities is a legal requirement for clinical trials and marketing of prescription drugs in the European Union.
Arandi has organized around-the-clock physician coverage for clinical trials and marketed products, responding to any calls and emails from study sites, laboratories, and  authorities.

 

 

Study logistics support

Since we have more than twenty years of hands-on management experience of clinical trials in Europe we can offer full project management services for phase I/II trials. This includes:
 
- Investigator recruitment & contracts
- Budgets,
- Site qualification visits & site training
- Regulatory agency & ethics committee contacts
- Pharmacy contacts
- Clinical trial applications.
- Feasibility investigations
- Pre-screening of patients
- Investigator site support, including planning & documenting the 
  patient’s site visits, archiving, SAE reports and follow-up.

   

Arandi Development AB • Karlbergsvägen 30, 113 27 Stockholm • Email: