DocShifter
Exhibiting Companies
Information
Accelerating regulatory document preparation in Life Sciences
Automate PDF conversion, enrichment and quality control.
- Scalable, compliant and fast
- On premise, or in your cloud
- Integrates seamlessly with all your existing systems
High volume, high-quality document conversion, on-premise or in the cloud.
Automation, compliance, quality, speed, dynamic scalability, and configurability is why life sciences companies of all sizes choose DocShifter. We support the regulatory teams by:
- Accelerating the drug submission process through automation of renditions for submission-ready PDF documents in eCTD submissions.
- Automating checks and fixes to Word and PDF files to ensure that pharma companies meet the most stringent technical requirements by the health authorities (FDA, EMA, PMDA, Health Canada).
- Automatically merging documents into a single PDF and generate (compliant) reports for submission and documentation. Including 510k and PMA medical device submissions.
- Converting all required digital files for storage in a long-term archive. PDF/A or the latest file format in use to ensure digital sustainability. For MS Office, image, audio and video files.