Precision. Compliance. Quality.

Pharmaceutical GMP Consulting, Auditing & Regulatory Compliance Advisory

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Introduction

Precise. Compliant. Reliable.

End-to-end GMP consulting and auditing for confident, inspection-ready operations.

Pharmaceutical process

Built around your products, processes, and markets.

Tailored solutions that align with your specific pharmaceutical operations and regulatory requirements.

Quality assurance

Clear findings. Actionable remediation.

Comprehensive assessments with practical recommendations for sustainable compliance improvements.

End-to-End GMP

From strategy to inspection readiness.

Our Services

GMP expertise, across the compliance lifecycle.

Practical, regulator-aligned services that strengthen quality systems and ensure inspection readiness.

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GMP Consulting & Advisory

Strategic guidance to design, scale, and optimize GMP-compliant operations aligned with global regulations.

GMP Auditing & Compliance Assessments

Comprehensive audits and assessments to identify gaps and ensure regulatory compliance across all operations.

Regulatory Inspection Readiness & Remediation

Prepare for regulatory inspections and implement effective remediation strategies for identified issues.

Quality Management Systems (QMS)

Design and implement robust quality management systems that meet international standards and best practices.

Validation & Qualification Services

Comprehensive validation and qualification services for equipment, processes, and facilities.

GxP & Pharmacovigilance Compliance

Ensure compliance with Good Practice guidelines and pharmacovigilance requirements across your organization.

Industries We Serve

GMP expertise across diverse life-sciences sectors.

Supporting compliance, quality, and inspection readiness across regulated industries.

Pharmaceutical Manufacturers

Pharmaceutical Manufacturers

API Manufacturers

API & Intermediate Manufacturers

Biotech Organizations

Biotech & Biologics Organizations

Medical Device Manufacturers

Medical Device Manufacturers

CMOs

Contract Manufacturing Organizations (CMOs)

CROs

Contract Research Organizations (CROs)

Why Threedpharma?

Trusted GMP expertise, built on clarity and integrity.

Independent, regulator-aligned support focused on practical outcomes and sustainable compliance.

  • Independent & Objective Audits

    Unbiased, third-party assessments delivering clear insights without conflict of interest.

  • Deep Regulatory Expertise

    Extensive knowledge of global pharmaceutical regulations and industry best practices.

  • Practical, Implementable Solutions

    Actionable recommendations that are realistic, cost-effective, and sustainable for your organization.

  • Risk-Based, Inspection-Ready Approach

    Proactive strategies that prioritize critical areas and ensure readiness for regulatory inspections.

  • Global Standards, Local Regulatory Insight

    Combining international best practices with deep understanding of local regulatory requirements.

  • Strict Confidentiality & Professional Integrity

    Maintaining the highest standards of confidentiality and ethical conduct in all engagements.

GMP Excellence

We don't just prepare you for audits. We help you build sustainable GMP excellence.

Global Reach

Delivering globally aligned GMP compliance with deep local regulatory understanding.

We support clients across

Middle East

Middle East

Asia

Asia

Europe

Europe

Africa

Africa

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