20+
Therapeutic areas
Therapeutic Areas
Deep expertise across indications
Validcare has delivered clinical trials across 20+ therapeutic areas—from women's health and oncology to metabolic disorders and rare diseases.
Our experience isn't just broad—it's deep. We understand the unique challenges of each therapeutic area: patient populations, endpoint selection, regulatory pathways, and site requirements. That expertise shapes how we design, execute, and deliver your trial.
Proven across therapeutic areas and study types
Since 2014, Validcare has supported sponsors in pharma, biotech, medical devices, and nutraceuticals—delivering trials that span early development through pivotal studies.
Global
Trials across Americas, Europe, Asia Pacific, MENA
All Phases
Phase I through Phase III and post-market
Areas of deep expertise
These therapeutic areas represent our deepest experience—where we've delivered multiple trials and developed specialized knowledge of patient populations, endpoints, and regulatory requirements.
Women's Health
Validcare has extensive experience in women's health trials spanning reproductive health, menopause, contraception, and maternal-fetal medicine. We understand the unique recruitment challenges, endpoint sensitivities, and regulatory considerations in this space.
Experience Includes:
- Reproductive health and fertility
- Menopause and hormone therapy
- Contraception studies
- Maternal-fetal medicine
- Gynecologic conditions
Oncology
From solid tumors to hematologic malignancies, Validcare supports oncology sponsors with trials designed for the complexity of cancer research. Our platform handles the intensive data requirements and safety monitoring that oncology trials demand.
Experience Includes:
- Solid tumor studies
- Hematologic malignancies
- Immuno-oncology
- Supportive care
- Survivorship studies
Cardiovascular
Cardiovascular trials require precise endpoint measurement, experienced sites, and careful safety monitoring. Validcare has delivered CV studies across risk factors, acute conditions, and device interventions.
Experience Includes:
- Lipid disorders and atherosclerosis
- Hypertension
- Heart failure
- Arrhythmia
- Cardiovascular devices
Endocrinology & Metabolism
Metabolic disorders—from diabetes to obesity to rare endocrine conditions—require deep understanding of biomarkers, patient adherence, and long-term outcome measurement. Validcare has delivered trials across the metabolic spectrum.
Experience Includes:
- Diabetes (Type 1 and Type 2)
- Obesity and weight management
- Thyroid disorders
- Metabolic syndrome
- Rare endocrine disorders
Neurology
Neurological trials present unique challenges in endpoint assessment, patient selection, and data capture. Validcare's platform supports the complex assessments and longitudinal monitoring that CNS studies require.
Experience Includes:
- Neurodegenerative diseases
- Movement disorders
- Epilepsy
- Neuropathic pain
- Multiple sclerosis
Gastroenterology
From inflammatory bowel disease to functional GI disorders, Validcare supports GI trials with expertise in patient-reported outcomes, endoscopic endpoints, and the recruitment challenges unique to this space.
Experience Includes:
- Inflammatory bowel disease (IBD)
- Irritable bowel syndrome (IBS)
- GERD and acid-related disorders
- Liver disease (NASH/NAFLD)
- Microbiome studies
Proven capability across indications
Beyond our areas of deepest expertise, Validcare has delivered trials across a broad range of therapeutic areas. Our platform and processes adapt to the specific requirements of each indication.
Allergy & Immunology
- Allergic rhinitis
- Atopic dermatitis
- Food allergy
- Autoimmune disorders
Dermatology
- Psoriasis
- Acne
- Wound healing
- Aesthetic indications
Infectious Disease
- Bacterial infections
- Viral infections
- Vaccine studies
- Antimicrobial resistance
Ophthalmology
- Dry eye disease
- Glaucoma
- Retinal disorders
- Ocular devices
Psychiatry & Sleep
- Depression and anxiety
- Schizophrenia
- Sleep disorders
- ADHD
Pulmonology
- Asthma
- COPD
- Pulmonary fibrosis
- Respiratory infections
Rheumatology
- Rheumatoid arthritis
- Osteoarthritis
- Lupus
- Gout
Nephrology & Urology
- Chronic kidney disease
- Overactive bladder
- BPH
- Kidney stones
Hematology
- Anemia
- Bleeding disorders
- Thrombosis
- Rare blood disorders
Orphan & Rare Diseases
- Ultra-rare conditions
- Pediatric rare diseases
- Natural history studies
- Expanded access
Pediatrics
- Pediatric formulations
- Growth and development
- Pediatric indications
- Age-appropriate endpoints
Vaccines
- Prophylactic vaccines
- Therapeutic vaccines
- Adjuvant studies
- Immunogenicity
Medical Device Expertise
Validcare supports medical device sponsors through IDE submissions, pivotal trials, and post-market surveillance—with understanding of device-specific regulatory pathways and endpoint requirements.
Diagnostic Devices
- In vitro diagnostics
- Imaging devices
- Monitoring systems
Therapeutic Devices
- Implantable devices
- Drug-device combinations
- Surgical instruments
Digital Health
- Software as Medical Device (SaMD)
- Connected devices
- Digital therapeutics
Nutraceutical & Food Studies
Validcare has deep experience in infant formula, dietary supplements, and functional food studies—understanding FDA and international regulatory requirements for food and nutrition research.
Infant Formula & Nutrition
- Infant formula studies
- Growth and tolerance
- Nutritional adequacy
- Regulatory submissions
Dietary Supplements
- Efficacy studies
- Safety assessments
- Bioavailability
- Structure/function claims
Functional Foods
- Health claim support
- Ingredient studies
- Consumer research
- Regulatory strategy
Supporting trials across the development continuum
From first-in-human through post-market, Validcare delivers trials designed for each phase of development.
1
Phase I
- First-in-human studies
- PK/PD studies
- Dose escalation
- Food effect studies
- Healthy volunteer studies
2
Phase II
- Proof-of-concept
- Dose-ranging studies
- Biomarker studies
- Signal detection
- Adaptive designs
3
Phase III
- Pivotal efficacy trials
- Multi-center global studies
- Regulatory submissions
- NDA/BLA support
- Pediatric studies
4
Phase IV / Post-Market
- Post-marketing commitments
- Real-world evidence
- Registry studies
- Long-term safety
- Observational research
Indication knowledge that shapes trial success
A CRO that doesn't understand your therapeutic area will learn on your timeline and your budget. Validcare brings indication expertise from day one.
Smarter Protocol Design
We know which endpoints regulators expect, which assessments work in practice, and which inclusion criteria will actually recruit. That knowledge shapes protocols that succeed.
Better Site Selection
We know which sites perform in each indication—not just who promises patients, but who actually delivers. Our feasibility is based on real experience, not database queries.
Faster Problem-Solving
When issues arise—and they always do—we've seen them before. Our teams recognize indication-specific challenges and resolve them faster because we've been there.
Therapeutic expertise, global reach
Validcare delivers trials across regions—with operational capabilities and regulatory knowledge in each geography.
Legal presence
Operational reach
8 Legal entities
40+ Countries
Americas 6 countries
Legal presence: USA
Operational: Canada, Argentina, Brazil, Chile, Mexico
Europe 10 countries
Legal presence: UK, Germany, Poland, Czechia
Operational: France, Italy, Spain, Hungary, Romania, Nordic countries
Asia Pacific 7 countries
Legal presence: Australia
Operational: New Zealand, Japan, Taiwan, Philippines, Singapore, Malaysia
MENA 3 countries
Legal presence: Israel, Turkey
Operational: Lebanon
Let's Discuss Your Trial
Ready to talk about your indication?
Tell us about your therapeutic area and study design. We'll share our relevant experience and show you how Validcare can deliver.