News & Updates

GxP and QMS setup for eClinical companies

GxP and QMS setup for eClinical companies

GxP and QMS setup for eClinical companies GxP and QMS setup for eClinical companies- (India) Clintask provides full QMS setup and operationalization support for Indian

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DPDP Act and GDPR compliance consulting

DPDP Act and GDPR compliance consulting

DPDP Act and GDPR compliance consulting DPDP Act and GDPR compliance consulting- (India) Clintask supports organizations in aligning their data management practices with India’s Digital

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Data privacy compliance under APPI and GDPR

Data privacy compliance under APPI and GDPR

Data privacy compliance under APPI and GDPR Data privacy compliance under APPI and GDPR- (Japan) Clintask’s data privacy team supports Japanese companies in implementing privacy-by-design

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GxP compliance for Japanese CROs

GxP compliance for Japanese CROs

GxP compliance for Japanese CROs GxP compliance for Japanese CROs- (Japan) Clintask’s bilingual experts assist Japanese CROs in aligning PMDA expectations with global GCP, GLP,

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CAPA and Quality metrics management

CAPA and Quality metrics management

CAPA and Quality metrics management CAPA and Quality metrics management Clintask’s CAPA management framework ensures deviations and audit findings are addressed through structured root cause

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Global

Validation as a Service

Validation as a Service Validation as a Service Clintask offers Validation as a Service globally, ensuring continuous CSV, periodic review, and change control management. Our

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Global

QaaS – Quality as a Service

QaaS – Quality as a Service QaaS – Quality as a Service Through Clintask’s QaaS model, organizations access virtual QA experts who perform audits, CAPA

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Global

Mock inspections & audit readiness

Mock inspections & audit readiness Mock inspections & audit readiness Clintask conducts mock inspections replicating FDA, EMA, and MHRA conditions to prepare sites for regulatory

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China

CSV and GDPR–China DSL compliance

CSV and GDPR–China DSL compliance CSV and GDPR–China DSL compliance- (China) Clintask assists Chinese CROs and CDMOs in integrating GxP CSV and data privacy requirements

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SEO

SLA QA & QC program

SLA QA & QC program SLA QA & QC program Clintask provides independent SLA QA and SLA QC oversight, ensuring service-level agreements are not only

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Uncategorized

QMS consulting for biotech

QMS consulting for biotech QMS consulting for biotech Clintask specializes in Quality Management System (QMS) implementation for biotech and eClinical organizations. From SOP creation, document

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CSV services for pharma

CSV Services for pharma (United States)

CSV Services for pharma (United States) CSV Services for pharma Clintask delivers full-spectrum Computer System Validation (CSV) solutions across laboratory, manufacturing, and clinical systems, ensuring

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news & updates

Forbes, India of the year 2024-2025

Prominent Companies of the year 2024-2025 Prominent Companies of the year 2024-2025 We are truly honored to share that Clintask Solutions has been recognized by

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news & updates

India Pharma Outlook 2024

India Pharma Outlook India Pharma Outlook We are thrilled to celebrate a momentous achievement as Clintask Solutions is proudly recognized and selected by India Pharma

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Clintask Solutions : Value Based Service

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