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Our Locations

Nottingham and London. We're a remote consultancy that endeavors to provide high quality solutions to regulatory partners.    

Tel: +447506975972  & +447734219260 

ectdpharma@outlook.com

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Find Us

Tel:  +447506975972  &  +447734219260

ectdpharma@outlook.com

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Cheryl.Allen@ectdpharma.com

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Thomas.Marsden@ectdpharma.com

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Offices based in London & Nottingham, United Kingdom

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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