Clinical Trials — From Early-Phase to Market-Ready Solutions
Integrated Expertise Across Therapeutic and Cosmetic Fields
QIMA Life Sciences offers end-to-end clinical development services designed to accelerate innovation across pharmaceutical, dermo-cosmetic, cosmetic, and nutraceutical markets.
Our multidisciplinary clinical network combines medical rigor, dermatological and cosmetic expertise, and analytical precision to support every stage of product evaluation — from early-phase trials to confirmatory studies.
We operate under full GCP compliance and collaborate closely with sponsors to design fit-for-purpose protocols, ensuring robust, reliable, and regulatory-aligned data.
With specialized sites across Europe and Latin America, we provide global reach combined with local regulatory insight.
Our teams deliver customized study designs, efficient volunteer recruitment, and comprehensive data management, helping sponsors bring safe and effective products to market faster.
Comprehensive Clinical Trial Capabilities
Our clinical teams manage a wide range of study types and therapeutic areas, including:
- Phase I to IV clinical trials
- Bioequivalence and pharmacokinetic studies
- Topical and transdermal drug development
- Dermo-cosmetic and cosmetic efficacy studies
- Nutraceutical and food supplement trials
- Medical device evaluations
This flexibility allows us to adapt our methodologies to each project’s unique objectives — from efficacy and safety demonstration to mechanism-of-action investigations or real-world performance assessments.
State-of-the-Art Clinical Infrastructure
Our facilities are equipped to handle both ambulatory and in-patient studies under stringent medical supervision.
Key assets include:
- 86 beds for overnight stays and continuous monitoring (BE & early-phase trials)
- Volunteer orientation lecture hall and dedicated drug administration rooms
- Emergency care station and access to Intensive Care Unit (ICU)
- Four secure pharmacies with biometric access
- Refrigerators & freezers (-20°C and -70°C)
- On-site analytical laboratories (biochemical, ECG, spirometry, vital signs monitoring)
- In-house Ethics Committee ensuring regulatory and ethical compliance
Our volunteer database includes over 200,000 registered participants, segmented by therapeutic area and indication, including both healthy subjects and patients.
We collaborate with specialized physicians across multiple disciplines, ensuring appropriate medical oversight for all clinical programs.
