Computer System Validation

CSV Services by Tech Qualitas

In the modern life sciences and regulated industries, computerised systems are the backbone of R&D, manufacturing, clinical trials, quality assurance, and pharmacovigilance. At Tech Qualitas, we help organisations achieve and maintain compliance by offering end-to-end Computer System Validation (CSV) services that are audit-ready, risk-based, and aligned with global regulatory standards.

With over 40 years of combined expertise, we have successfully supported numerous clients in validating critical systems — ensuring data integrity, patient safety, and product quality throughout the system life cycle.

Computer System Validation | Tech Qualitas

Why CSV Matters

Unvalidated systems can jeopardise:

  • Compliance with 21 CFR Part 11, EU Annex 11, GAMP 5, ISO 13485

  • Regulatory inspection outcomes

  • Data traceability and security

  • Business continuity and operational quality

Computer System Validation ensures:

  • Your systems function as intended

  • Risks are identified and mitigated

  • Documentation is compliant and audit-ready

  • Lifecycle control and change management are maintained

Our CSV Services

We deliver a full spectrum of CSV services tailored to system complexity and risk, including:

  • CSV risk assessment and planning

  • 21 CFR Part 11 and Annex 11 GAP analysis

  • GxP applicability assessments

  • SDLC development or optimisation
  • Validation planning and project execution
  • Creation of URS, FS, DS, and traceability matrices
  • Development of validation protocols (IQ, OQ, PQ)
  • Controlled execution and deviation handling
  • Validation Summary Report (VSR) delivery
  • Application-specific validation audits
  • Data centre qualification
  • Backup and disaster recovery validation
  • Business continuity and IT security review
  • Periodic review and revalidation
  • Legacy system retrospective validation
  • Change control, incident management, and audit trail assessments
  • Integration with QMS and SOP governance

Tech Qualitas CSV Methodology

Our scalable and proven CSV methodology follows a process-oriented and risk-based approach. Inspired by GAMP 5 and international regulatory standards, our validation framework includes:

  • Standard Operating Procedures (SOPs)
  • Document templates for each lifecycle phase
  • Testing tools and best practices
  • Training modules for internal teams
  • Integration into your existing SDLC and QMS

Common Causes of CSV Failure

  • Lack of a structured plan

  • Poor documentation and traceability

  • Inadequate testing and coverage

  • Weak risk management processes

How We Help You Avoid Them

Tech Qualitas partners with clients to build comprehensive validation plans, ensure documentation excellence, execute robust testing, and apply industry-standard risk controls to keep your systems validated and compliant.

Validated System Types We Support

  • ERP, QMS, LIMS, DMS, LMS

  • Clinical Trial and PV Systems

  • Custom-built applications and SaaS solutions

  • Cloud-hosted platforms and spreadsheets

Why Choose Tech Qualitas?

Expertise You Can Trust
Decades of hands-on experience with validated systems across multiple regulated industries.

Inspection-Ready Documentation
Our deliverables meet the highest standards and are designed to withstand the scrutiny of regulatory inspections.

Tailored Solutions
From full-service validation to modular consulting packages, our approach adapts to your needs.

Risk-Based, Cost-Effective Execution
Focused on quality and compliance without excessive cost or time burden.

Training & Knowledge Transfer
We empower your team through dedicated training, ensuring sustainability of compliance practices.

Neeru Bakshi

Founder






    Expert quality and compliance solutions for organizations with efficiency as a priority.

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