Qdossier

Over Qdossier

Proper management of data, documents and dossiers saves the pharmaceutical industry and agency time and money. Qdossier takes complete ownership and is fully committed to create compliant submissions right first time. We understand the importance of technical- and business validation of regulatory dossiers. Our business knowledge, clear communication and approach towards information ensures that our sponsors can remain focused on their core business. We manage and implement eCTD, NEES, DMF, XEVMPD and IDMP across product types and countries, using sponsor's tools or our own tools, remote or onsite. Looking forward to hear about your challenges so we can offer help.

Trefwoorden

• Brexit
• Cmc Authoring
• Data Migration
• Document Migration
• Document Templates
• Dossier Migration
• Due Diligence
• Ectd
• Ectd Viewing Tool
• Hosting
• Idmp
• Lean Authoring
• Medical Writing
• Module 3 Baselines
• Procedural Support
• Process Development
• Regulatory Information Management
• Regulatory Operations
• Regulatory Strategy
• Structured Content Management
• Submission Management

Adres

• Hoofdkantoor

  Cartografenweg 28C5141MT WaalwijkNoord-Brabant, Nederland

Team per functiegebied

Gebaseerd op 8 openbare functieprofielen, stand van 3 september 2026.

• Legal / Compliance6
• Product Management1
• Research / R&D1