Clientele

We serve

Clintask supports CROs, Biopharma, eClinical, medical device companies and IT service providers with quality, compliance and validation services.

CROs (Contract Research Organisations)

GCP audits, investigator site and vendor audits, inspection readiness and quality support for clinical research and CRO operations.

Biopharma

Quality, compliance and validation services for pharmaceutical and biopharmaceutical organisations, including GxP audits, quality management systems and pharmacovigilance SLA/QC compliance.

eClinical

Computerised system validation, quality management systems and GDPR/HIPAA assessments for eClinical companies and products, including EDC and ePRO/eCOA systems.

Medical Devices

Quality and compliance support for medical device companies, with a focus on regulatory requirements, quality management and operational efficiency.

IT and IT-Enabled Services

Audit, validation and data privacy assessment support for IT service providers and computerised systems used in life sciences.

Our clients

Trusted by 25+ life science organisations across the USA, China, India, Japan and Europe

25+Life-science organisations4Sectors served5Regions: USA, China, India, Japan, Europe
Global Pharma
  • Biopharmaceutical company: India | Mock US FDA inspection
  • US affiliate of a global pharmaceutical: USA | GCP, GLP and GMP audits
  • Global specialty pharmaceutical: Europe | GCP and GCLP audits
Biotech
  • Clinical-stage biotech, genetic medicines: USA | GCP and GLP audits
  • Clinical-stage biotech, rare diseases: USA | GCP and GLP audits
  • Clinical-stage biotech, oncology: USA | GCP and GLP audits; GLP safety and toxicology audits
  • Clinical-stage biotech, RNA therapeutics: USA | GCP and GLP audits
  • Clinical-stage biotech, immuno: USA | GCP audits, eTMF QC and inspection readiness
  • Clinical-stage biotech, ophthalmology: USA | GCP audits
  • Pre-clinical stage biotech: USA | GLP safety and toxicology audits
  • Pre-clinical biotech: USA | GCP and GLP audits
  • Clinical-stage biotech: USA | GLP audits; GCP audits
CROs & Service Providers
  • Clinical data and biostatistics CRO: USA | GDPR assessment of eClinical products
  • Clinical research organisation: India | GCP gap assessment audit
  • Functional service provider: USA | Multiple GxP services
eClinical & Technology
  • eClinical technology: USA | QMS, CSV/CSA release validation and client audit support
  • Global IT services (life-sciences): Global | Medical device CSV and validation support
  • eClinical Technology Data and Analytics: India | GCP gap assessment audit
  • Life-sciences training and engagement platform: USA | CSV/CSA to GxP requirements
  • Technology company: USA | Life-science consulting

Years of cumulative experience

Unique Collaborations

Service lines

Countries served