eCTD Submissions & Lifecycle Management
CTR &
CTIS Support
CTIS Support
Word & PDF Publishing,
CTD Templates
CTD Templates
Regulatory Intelligence
Here
to get your
science
there
We Make Complex Regulatory Submissions Simple
Simplify eCTD Submissions: Overcome complexity and reduce costs with expert guidance.
Avoid Delays and Rejections: Collaborate with our experts for streamlined processes.
Expert Partnerships: Working with Pharmaceuticals, Biotech, Medical Devices, CROs, and Regulatory Consultants.
Guaranteed Timeliness: We've never missed a deadline or had an eCTD technical rejection.
Measured by Your Success: From strategy through submission to post-approval maintenance, we're measured by your success. Our global expertise spans major markets including FDA, EMA and MHRA submissions.
Avoid Delays and Rejections: Collaborate with our experts for streamlined processes.
Expert Partnerships: Working with Pharmaceuticals, Biotech, Medical Devices, CROs, and Regulatory Consultants.
Guaranteed Timeliness: We've never missed a deadline or had an eCTD technical rejection.
Measured by Your Success: From strategy through submission to post-approval maintenance, we're measured by your success. Our global expertise spans major markets including FDA, EMA and MHRA submissions.
Let's Connect
Why Canopy?
- Trusted Industry Partner: Serving the Life Sciences community for over 15 years with more than 250 clients.
- Global eCTD Expertise: Benefit from our extensive experience in preparing and managing eCTD submissions across multiple regulatory regions, ensuring compliance and efficiency in your global drug approval processes.
- Proven Success: Rely on our 25+ years of eCTD experience and over 4,000 successful submissions with a 100% technical approval rate.
- Focus on Your Core Priorities: Stay dedicated to science, research, and your team while we manage all your Regulatory Operations.
