Sara Soroush Tiedemann +45 26116630

Sara Soroush Tiedemann +45 26116630

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    • Home
    • About Us
    • Our Services
    • Careers
      • Open positions
    • Contact Us
  • Home
  • About Us
  • Our Services
  • Careers
    • Open positions
  • Contact Us

We offer

Our Mission

Flexible Engagement

Our Mission

Our mission is to strengthen pharmaceutical production and project execution by delivering practical, compliant, and high‑quality solutions. We bridge the gap between operations, quality, and engineering, ensuring that our clients achieve reliable processes, successful projects, and sustained GMP compliance.

Our Team

Flexible Engagement

Our Mission

Our team brings extensive experience from pharmaceutical production, quality assurance, and engineering projects. We combine hands‑on operational knowledge with a strong understanding of GMP requirements, enabling us to solve complex challenges efficiently and deliver reliable results for our clients.

Flexible Engagement

Flexible Engagement

Flexible Engagement

We support pharmaceutical companies with expert guidance in production, quality, and technical projects. Our services include process support, GMP compliance, equipment qualification, documentation, and project execution.

Our Core Areas

Quality Assurance & Compliance (GXP)

Optimizing Manufacturing Processes

We support pharmaceutical production by improving process flow, reducing downtime, and strengthening GMP compliance. Our expertise ensures reliable operations, consistent product quality, and efficient troubleshooting of manufacturing challenges.

Project Management Back log Reduction Regulatory Affairs

Ensuring Equipment and Facilities Readiness

We support pharmaceutical production by improving process flow, reducing downtime, and strengthening GMP compliance. Our expertise ensures reliable operations, consistent product quality, and efficient troubleshooting of manufacturing challenges.

Engineering and Technical Support Clinical & Medical Affairs

Strengthening Documentation and Regulatory Alignment

We prepare and update essential GMP documents such as SOPs, protocols, reports, and risk assessments. Our support ensures documentation accuracy, audit readiness, and alignment with both internal and regulatory standards.

Manufacturing, Qualifications, Validation & Tech Transfer

Managing Projects From Design to Handover
We provide expertise across the full project lifecycle—planning, execution, commissioning, qualification, and handover. Our structured approach ensures that timelines, budgets, and compliance requirements are consistently met.

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Pharma Consulting ApS

+45 26116630

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