News | Ectd Pharma

top of page

Green Gradient Technology ProfessionalBu

Home
Services
Contact Us
Meet the Team
FAQ's
News
Training
More

Use tab to navigate through the menu items.

ECTD Pharma News

All Posts

Search

From NeeS to eCTD: The Digital Transformation of Pharmaceutical Submissions

From NeeS to eCTD: The Digital Transformation of Pharmaceutical Submissions

From NeeS to eCTD: The Digital Transformation of Pharmaceutical Submissions

May 17, 20255 min read

From Paper to Approval: The Power of Regulatory Publishing Services for Medical Devices

From Paper to Approval: The Power of Regulatory Publishing Services for Medical Devices

From Paper to Approval: The Power of Regulatory Publishing Services for Medical Devices

May 9, 20253 min read

Top 5 eCTD Submission Mistakes and How Our eCTD and Regulatory Publishing Services is at the forefront

Top 5 eCTD Submission Mistakes and How Our eCTD and Regulatory Publishing Services is at the forefront

Top 5 eCTD Submission Mistakes and How Our eCTD and Regulatory Publishing Services is at the forefront

Apr 26, 20253 min read

Sequence 0001 and Beyond: How eCTD Pharma is Navigating the FDA’s New Submission Frontier

Sequence 0001 and Beyond: How eCTD Pharma is Navigating the FDA’s New Submission Frontier

Sequence 0001 and Beyond: How eCTD Pharma is Navigating the FDA’s New Submission Frontier

Apr 25, 20254 min read

Key Challenges for Life Sciences, Biotech, and Pharma companies in 2025

Key Challenges for Life Sciences, Biotech, and Pharma companies in 2025

Key Challenges for Life Sciences, Biotech, and Pharma companies in 2025

Apr 21, 20254 min read

Custom Solutions for Every Client!

Custom Solutions for Every Client!

Custom Solutions for Every Client!

Apr 17, 20253 min read

Why Small and Mid-Sized Regulatory Consultancies Rely on Expert Regulatory Publishing Services

Why Small and Mid-Sized Regulatory Consultancies Rely on Expert Regulatory Publishing Services

Why Small and Mid-Sized Regulatory Consultancies Rely on Expert Regulatory Publishing Services

Apr 16, 20253 min read

How AI Will Transform Regulatory Affairs Over the Next Decade — and Why eCTD Remains the Cornerstone

How AI Will Transform Regulatory Affairs Over the Next Decade — and Why eCTD Remains the Cornerstone

How AI Will Transform Regulatory Affairs Over the Next Decade — and Why eCTD Remains the Cornerstone

Apr 11, 20254 min read

Having trouble getting your product to market?

Having trouble getting your product to market?

Having trouble getting your product to market?

Apr 5, 20253 min read

ECTD Pharma: Your Premier Regulatory Publishing Consultancy for Expert eCTD Publishing

ECTD Pharma: Your Premier Regulatory Publishing Consultancy for Expert eCTD Publishing

ECTD Pharma: Your Premier Regulatory Publishing Consultancy for Expert eCTD Publishing

Mar 31, 20254 min read

FDA’s ESG NextGen: A New Era for eCTD Submissions & How ECTD Pharma Consultants Can Help

FDA’s ESG NextGen: A New Era for eCTD Submissions & How ECTD Pharma Consultants Can Help

FDA’s ESG NextGen: A New Era for eCTD Submissions & How ECTD Pharma Consultants Can Help

Mar 30, 20253 min read

Embracing FDA’s DTD v4.0: How ECTD Pharma Leads the Way in Regulatory Submissions

Embracing FDA’s DTD v4.0: How ECTD Pharma Leads the Way in Regulatory Submissions

Embracing FDA’s DTD v4.0: How ECTD Pharma Leads the Way in Regulatory Submissions

Mar 27, 20253 min read

The Strategic Advantage of Outsourcing eCTD Regulatory Submissions to a Specialized Consultancy

The Strategic Advantage of Outsourcing eCTD Regulatory Submissions to a Specialized Consultancy

The Strategic Advantage of Outsourcing eCTD Regulatory Submissions to a Specialized Consultancy

Mar 26, 20253 min read

The birth of ECTD submissions

The birth of ECTD submissions

The birth of ECTD submissions

Mar 18, 20253 min read

What is ECTD publishing and why it's a key part of regulatory affairs

What is ECTD publishing and why it's a key part of regulatory affairs

What is ECTD publishing and why it's a key part of regulatory affairs

Mar 7, 20252 min read

Streamline Your Regulatory Process with ECTD Pharma

Streamline Your Regulatory Process with ECTD Pharma

Streamline Your Regulatory Process with ECTD Pharma

Mar 3, 20251 min read

Navigating FDA Queries: ECTD Pharma's Technical Support Solutions

Navigating FDA Queries: ECTD Pharma's Technical Support Solutions

Navigating FDA Queries: ECTD Pharma's Technical Support Solutions

Mar 3, 20251 min read

Expert Tips for Flawless eCTD Submissions

Expert Tips for Flawless eCTD Submissions

Expert Tips for Flawless eCTD Submissions

Mar 3, 20252 min read

Find Us

Tel: +447506975972 & +447734219260

ectdpharma@outlook.com

Cheryl.Allen@ectdpharma.com

Thomas.Marsden@ectdpharma.com

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.

bottom of page