Specialized Services

Specialized Services

Specialized Services

Data integrity failures can damage regulatory approvals and long-term business trust. We provide specialised services designed to control data integrity risks across pharmaceutical, API, and biotechnology manufacturing units. Our structured packages help strengthen documentation control, system validation, and ethical data practices. We align our support with USFDA, EU GMP, MHRA, TGA, MFDS, COFEPRIS, HEALTH CANADA and PMDA expectations. Our focus remains on building reliable systems that protect electronic and paper records from manipulation, loss, or regulatory concern.

Our first package begins with detailed gap analysis of existing data management practices. We review audit trails, access controls, backup systems, and documentation flow. After identifying weaknesses, we prepare clear and practical SOPs that define data handling responsibilities. Strong procedures reduce human error and prevent regulatory observations. This foundation creates a controlled and traceable documentation environment.

Our second package addresses software controls and computer system validation. We evaluate electronic systems used in laboratories, manufacturing, and quality functions. Validation ensures systems operate as intended and maintain secure data storage. When systems lack validation, regulatory risk increases. We guide structured validation protocols, testing procedures, and documentation to strengthen compliance confidence.

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Our third package focuses on data integrity policies and ethics training. We help establish written policies that define acceptable data practices and escalation processes. Training programmes build awareness around audit trail review and ethical conduct. When personnel understand the impact of poor data practices, behaviour improves naturally. Compliance becomes a shared responsibility across departments.

Our fourth package provides retrospective data verification of electronic and paper records. We review historical records to identify inconsistencies and potential compliance gaps. Corrective actions are implemented to strengthen long-term system reliability. Our specialised services protect regulatory approvals and ensure sustainable data integrity across operations.

What CPC Offers

How Can We Help You?

We protect your organisation from data integrity risks through structured controls and disciplined documentation systems. Our support strengthens compliance stability across electronic and paper records.

We work closely with your teams to embed ethical data practices, validated systems, and sustainable inspection readiness.

Chemical Specialised Services Support

Chemical Specialised Services Support

  • Data Integrity Gap Analysis for Chemical Manufacturing
  • SOP Preparation for Laboratory and Production Controls
  • Electronic Record and Audit Trail Review
  • Computer System Validation for Analytical Software
  • Impurity Data Verification and Documentation Control
  • Retrospective Batch Record Review and Correction
  • Data Governance Policy Development
  • Risk Assessment for Electronic and Paper Records
  • Ethics and Compliance Training for Chemical Units
  • Remediation Planning After Data Integrity Findings
Biotech Specialised Services Support

Biotech Specialised Services Support

  • Data Integrity Assessment for Biotech Facilities
  • SOP Development for Controlled Bioprocess Documentation
  • Computer System Validation for Biotech Control Systems
  • Audit Trail Review for Laboratory Information Systems
  • Contamination Data Record Verification
  • Retrospective Electronic Data Review and Correction
  • Data Governance and Ethical Practice Framework
  • Risk-Based Data Integrity Monitoring Systems
  • Training on Ethical Data Handling in Biotech Operations
  • Regulatory Remediation Support for Data Observations
Pharmaceutical Specialised Services Support:

Pharmaceutical Specialised Services Support:

  • Data Integrity Gap Assessment for Drug Manufacturing Units
  • SOP Preparation for Quality and Production Documentation
  • Computer System Validation for eQMS Platforms
  • Audit Trail Review for Manufacturing and Laboratory Systems
  • Retrospective Batch and Analytical Record Verification
  • Data Integrity Policy and Governance Framework Development
  • Risk Evaluation of Electronic Documentation Systems
  • Ethics and Compliance Awareness Training
  • Corrective and Preventive Action Planning for Data Issues
  • Long-Term Data Integrity Monitoring and Compliance Strengthening