Onboard Our Consultants

Seamless Onboarding for eCTD Consulting & Submission Support

At eCTD Pharma, we offer flexible, expert regulatory support by integrating seamlessly into your existing workflows. Whether you use AWS, cloud-based regulatory platforms, or internal submission systems, we can be onboarded directly into your projects to provide specialized eCTD submission expertise on a consultant basis.

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How Our Onboarding Process Works

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We make it easy for pharmaceutical, biotech, and medical device companies to leverage our expertise without disrupting their internal processes. Our onboarding process includes:

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• Secure Integration – We can be granted access via AWS, VPN, or other secure gateways to work directly within your submission platforms.

• Use of Your Preferred Software – Our experts are proficient in various eCTD publishing and validation tools, ensuring we fit seamlessly into your workflow.

• Regulatory Compliance & Best Practices – We bring in-depth global regulatory knowledge while aligning with your internal compliance protocols.

• Dedicated Submission Support – Whether you need full submission management or ad-hoc consultancy, we provide the expertise you need, when you need it.

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Why Choose eCTD Pharma for Consultant-Based Submission Support?

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• Fully Remote & Secure Access – Work with us from anywhere via secure cloud-based platforms.

• Expertise Across Multiple Health Authorities – FDA, EMA, MHRA, Health Canada, Swissmedic, and more.

• Cost-Effective & Scalable Support – Flexible consultancy services that adapt to your project needs.

• End-to-End Submission Expertise – From initial dossier preparation to final eCTD publishing and validation.

• Minimal Disruptions to Your Workflow – We integrate smoothly into your processes, avoiding delays or operational changes.

Leverage Our Expertise Within Your Regulatory Systems

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With eCTD Pharma, you gain access to leading regulatory professionals who can work directly within your own submission infrastructure. Whether it’s a single submission or ongoing lifecycle management, we provide the knowledge, efficiency, and precision needed for successful regulatory approvals.

Get in touch today to onboard our regulatory experts and streamline your eCTD submissions!