Cliantha Research Limited

Overview

Cliantha Research Limited is a full-service Clinical Research Organization (CRO) based in Ahmedabad, India, established in 2004. The company specializes in providing comprehensive clinical development services to pharmaceutical, biotech, and healthcare companies. It is committed to ethical research practices and operates under the motto "Science with Integrity." With over 1,000 professionals, the organization has a strong track record of regulatory compliance, having been inspected by major authorities such as the USFDA, EMA, and WHO.

Cliantha offers a range of integrated clinical research solutions, including early-phase studies like Bioavailability-Bioequivalence and Phase I trials, as well as late-phase trials (Phases II-IV). Their specialized studies cover areas such as respiratory research, dermatology, and consumer research. Additionally, Cliantha provides laboratory and technical services, including pharmacovigilance and biometrics, supporting clinical development needs across North America, India, and other regions. The company has expanded its global presence through strategic acquisitions and operates advanced clinical sites and bio-analytical labs in multiple countries.

Basic Information

Contact Details

• Phone: +91 79268 53088
• Website: cliantha.com
• LinkedIn: linkedin.com/company/cliantharesearch

Key Focus Areas & Initiatives

• clinical trials
• central reference lab
• dermatology
• oncology
• bioanalytical
• immunochemistry
• phase i
• phase ii iv
• clinical laboratory
• biometrics
• early phase
• late phase
• consumer research
• data management
• cdisc
• biosimilars
• ba be
• respiratory
• tobacco research
• pharmaceuticals
• life sciences
• research services
• clinical data management platform (codeangelo)
• services
• clinical trial management
• gcp compliant clinical sites
• patient recruitment
• b2b
• clinical project management
• clinical site operations
• bioanalytical laboratories
• north america cro
• specialized dermatology testing
• regulatory audits by usfda, ema, who
• cap accreditation
• clinical study support
• cro
• drug development support
• therapeutic areas
• healthcare
• data management solutions
• bioequivalence studies
• clinical monitoring
• tobacco research studies
• clinical research consulting
• pharmacovigilance services
• drug development
• clinical trial site management in multiple countries
• clinical data analysis
• regulatory submissions
• india cro
• clinical research innovation
• pharmacokinetics
• global presence
• usfda inspection
• clinical data management
• early phase clinical trials
• environmental exposure chambers (eecs)
• pharmaceutical services
• clinical laboratory services
• cdisc data standards
• pharmaceutical industry
• clinical research quality assurance
• in vitro release testing (ivrt)
• global clinical trial support
• clinical trial feasibility studies
• biostatistics
• cro services
• consulting
• clinical research regulatory affairs
• clinical trial monitoring
• clinical research infrastructure
• ivrt testing
• clinical sites
• late phase clinical trials
• patient-centric clinical trial services
• regulatory inspections
• regulatory strategy consulting
• medical services
• veterinary therapeutics research
• europe cro
• regulatory compliance
• pharmacodynamics
• canada cro
• biotech research
• regulatory audits
• biotechnology
• advanced clinical laboratory infrastructure
• data management systems
• gcp compliance
• environmental allergen challenge models
• market research
• long housing studies
• therapeutic expertise
• veterinary therapeutics
• clinical research training
• clinical site management
• environmental exposure chambers
• bioanalytical lab
• bioequivalence / bioavailability studies
• clinical research technology
• medical and diagnostic laboratories
• bioanalytical services
• clinical trial logistics
• clinical research
• nabl accreditation
• clinical trial technology
• gcp standards
• medical laboratories
• clinical research outsourcing
• clinical research organization
• early phase studies
• late phase studies
• respiratory studies
• dermatology research
• eclinical
• elearning
• clinical study management
• phase i trials
• phase ii trials
• phase iii trials
• phase iv trials
• safety testing
• efficacy testing
• laboratory services
• immunogenicity testing
• study design
• statistical analysis
• volunteer recruitment
• patient safety
• risk mitigation
• quality assurance
• protocol development
• data analysis
• clinical operations
• biosimilar studies
• digital therapeutics
• academic partnerships
• cross-functional teams
• healthcare research
• education
• health care
• health, wellness & fitness
• hospital & health care
• medical
• medical & diagnostic laboratories
• medical practice
• e-learning
• internet
• information technology & services
• computer software
• education management
• data analytics

Technologies Used

• Amazon AWS
• Apache
• Bootstrap Framework
• Facebook Custom Audiences
• Facebook Login (Connect)
• Facebook Widget
• Google Font API
• Google Maps
• Google Tag Manager
• Microsoft Office 365
• Mobile Friendly
• Outlook
• Remote
• SendInBlue
• Sendgrid
• Ubuntu
• YouTube
• reCAPTCHA