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Consultation Audit for pharmaceuticals Industry

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Consultation Services – 4D Technologies

ISO/IEC 17025 is the international standard for the competence of testing and calibration laboratories. Whether your laboratory is involved in research, quality control, or compliance testing, obtaining ISO 17025 accreditation ensures that you meet the highest quality standards in the industry. At 4D Technologies, we provide expert ISO 17025 audit consultation to help laboratories prepare for successful accreditation and maintain their compliance with global standards.

Consultation for WHO Audit

A WHO audit evaluates every aspect of a company’s operations, from manufacturing processes and quality assurance to documentation and regulatory compliance. It’s essential for:

  • Global Market Access – WHO certification opens doors to international markets, ensuring products meet international health standards.
  • Compliance with Health Guidelines – Meeting WHO’s strict standards is essential for maintaining public trust and safety.
  • Building Reputation – WHO certification demonstrates a commitment to quality, safety, and regulatory compliance.
  • Audit Success – Proper preparation minimizes the risk of audit failures, non-compliance issues, and delays in product approval.

Consultation for PIC/S Audit

The Pharmaceutical Inspection Co-operation Scheme (PIC/S) sets some of the most stringent global standards for Good Manufacturing Practices (GMP) in the pharmaceutical industry. Companies seeking to operate internationally or export medicines to PIC/S member countries must be fully prepared for PIC/S inspections and audits. At 4D Technologies, we provide expert PIC/S Audit Consultation Services that help pharmaceutical companies achieve, maintain, and demonstrate compliance with these rigorous standards.

  • Audit-ready systems that pass international inspections
  • Comprehensive gap analysis and corrective action planning
  • Enhanced staff readiness and compliance culture
  • Reduced risk of audit failures and penalties
  • Stronger market positioning through global GMP recognition

Consultation for ISO 17025 Audit

ISO/IEC 17025 is the internationally recognized standard that specifies requirements for the competence of testing and calibration laboratories. Achieving ISO 17025 accreditation demonstrates that a laboratory operates with the highest standards of quality, reliability, and technical competence. At 4D Technologies, we provide expert ISO 17025 Audit Consultation Services to help pharmaceutical and analytical laboratories achieve and maintain compliance with this globally respected standard.

  • Increased confidence in test data and calibration results
  • Enhanced laboratory credibility and global recognition
  • Fully compliant and audit-ready laboratories
  • Reduced risk of audit failures and penalties
  • Continuous improvement through strong QMS implementation

Consultation for international drug ragulaty authoritirs

Expanding into international pharmaceutical markets requires strict compliance with the regulations of global drug regulatory authorities. Each country has its own framework, submission requirements, and compliance standards that must be met for product approval and market entry. At 4D Technologies, we provide expert consultation services to help pharmaceutical companies navigate the complex requirements of international drug regulatory authorities, ensuring smooth registrations and faster approvals.

  • Faster approvals and smoother registrations across multiple countries
  • Full compliance with ICH, WHO, FDA, EMA, and regional guidelines
  • Reduced risk of regulatory rejection and costly delays
  • Global expansion opportunities for your pharmaceutical products
  • End-to-end support from submission to post-approval maintenance
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