Manage clinical trials, track quality processes and organize regulatory submissions.
A single solution for document, label, and structured content management.
Organize, collaborate and review documents with your team online.
Quickly create documents with pre-made forms and templates.
Boost productivity with automated workflows, notifications and reporting.
Create and manage submission documents, manage administrative and archiving tasks more efficiently.
Connect all trial participants and processes in a single application and ensure best practices by documenting all activities.
Assign automatic quality control workflows while using risk assessment tools to identify and counter threats before they happen.
Automatically manage workflows for the review, approval, and periodic review of your SOP documents.
Tailored specifically to the needs of regulatory and related stakeholders, EXTEDO’s business process and regulatory consulting services are designed to support you during and after your eCTD submissions. Through a series of workshops, our team of experienced consultants will establish your business needs, understand your processes, and help you to define the most appropriate implementation approach.
To ensure you get the most out of your purchased solution, we offer detailed training for each product within the EXTEDOpulse solution portfolio. Training sessions are tailored to your individual needs and cover a broad range of technical and regulatory topics.
Purchasing a new EXTEDO application is the first step to streamlining business and regulatory processes within your organization. However, ensuring correct installation, implementation and integration is a crucial step in the process of deploying your new solution.