Services

With our committed subject matter experts, Qdossier supports Life Science organizations with the management of recordings and documentation of regulated information across data, documents, and dossiers.

We provide regulatory outsourcing services and can take either full responsibility of regulatory deliverables or engage remotely and/or on-site in operational activities within your company. Our team has vast experience with the compilation, submission, and maintenance of regulatory dossiers, registration tracking, IDMP/XEVMPD and document- and data migration.

Our areas of expertise are:

• Submission management
• Document authoring
• Local regulatory affairs
• Hosted submission management platform
• Registration tracking
• XEVMPD (and IDMP)
• Document- and data migration