Clinical Trials Supported
Community Partner
New Cancer Patients in 2023
Facility Info
- +34 932 54 50 30
- Monday - Friday | 8am - 4pm CEST
- Avinguda de Vallcarca, 151, 08023 Barcelona, Spain
Founded in 2022 by START, HM Nou Delfos Hospital, Dr. Emiliano Calvo and Dr. Tatiana Hernández-Guerrero, the START Barcelona facility is newly-renovated with ~350 sq meters of dedicated research space and a quickly growing team of clinical research experts, led by Principal Investigator Dr. Tatiana Hernández.
Explore START Barcelona's Clinical Trials
Phase I Clinical Trials
START Barcelona Nou Delfos has an on-site laboratory that can perform same day testing. This includes:
- CBC
- CMP
- UA with microscopy
- Thyroid panels
- Select Hepatitis panels
Clinical Laboratory
- CBC
- CMP
- PT/INR; PTT
- Tumor markers
- UA with microscopy
- Thyroid panels
- Select Hepatitis panels
- Troponin
Clinical Equipment
All equipment is annually inspected and calibrated and includes:
- Crash cart complete with intubation equipment
- Infusion pumps
- Syringe pumps
- Electronic vital signs monitoring
ECGS
Our clinicians have experience with utilizing ELI 150 and ELI 250 equipment from central vendors
Investigational Drug Section (IDS)
Pharmacy Equipment
- Biological safety cabinets
- Negative pressure clean room
- Positive pressure anteroom
- Secure medication storage room with continuous temperature monitoring
- Pharmaceutical grade -20°C freezers
- Room temperature storage shelving (20-25°C)
- All equipment is annually inspected and calibrated
Pharmacokinetics
Biopsy Specimens
PK department staff are IATA shipping certified. Specimens may be shipped same day, weekly, or monthly.
Laboratory Equipment
All equipment is annually inspected and calibrated and includes the following:
- Refrigerated / room temperature centrifuges
- Microfuges with refrigeration/room temp.
- -80°C / -20°C freezer with continuous temperature monitoring
- Refrigerator
- Room temperature storage shelving
- Dry ice delivered twice a week
Regulatory Affairs & Data Management
The Regulatory Affairs Department ensures compliance with all regulatory and industry requirements by following FDA and GCP guidelines for every study.
- Rapid IRB review and approval turnaround
- Competitive start-up timelines
The dedicated Data Management team ensures clean, accurate, and timely data entry and query resolution.
- Experience with a wide variety of electronic data capture systems (i.e., Medidata RAVE, InForm, Veeva, etc.)
- Monitoring suites with high speed Internet access
facility Tour of START Barcelona
facility Tour of START Barcelona
