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Improve your team with industry expert training 

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  • At ECTD Pharma, we deliver practical, industry-focused training designed to build real-world regulatory and eCTD publishing capability.

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  • Our courses are created and delivered by regulatory professionals with hands-on experience supporting global pharmaceutical, biotech, and life sciences organisations. We focus on how regulatory work is actually done in practice, not just theory.

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  • Whether you are new to regulatory affairs, transitioning into eCTD publishing, or strengthening existing expertise, our training provides clear, structured learning aligned to current industry expectations.

EMEA
MHRA
FDA
swissmedic
Health CA

Regulatory Submission Services | eCTD Publishing Experts – eCTD Pharma
At eCTD Pharma, we deliver industry-leading regulatory submission services tailored for the pharmaceutical, biotech, and healthcare sectors. Our expertise in eCTD publishing, regulatory gap analysis, and legacy submission conversions ensures your submissions are 100% compliant with EMA, FDA, and global health authority standards. Using advanced Freyr software, we provide fast, accurate, and secure electronic submissions, reducing approval timelines and minimizing compliance risks. Whether you need end-to-end eCTD submission support, lifecycle management, or expert consultancy, eCTD Pharma is your trusted partner. Maximize compliance. Minimize delays. Accelerate approvals. Contact eCTD Pharma today to streamline your regulatory process.

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