DocShifter

High volume, high-quality document conversion, on-premise or in the cloud. Automation, compliance, quality, speed, dynamic scalability, and configurability is why regulated enterprises choose DocShifter. In Life Sciences, 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...

Document refresh,web viewing,regulatory compliance,long term archiving,hi-fidelity rendering,data transformation,pdf transformation,ectd,document management,document management for life sciences,regulatory software solution,e-submission management,e-submission,regulatory information management,regulatory submission software,pdf,pdf/a,electronic regulatory submissions,pdf conversion,ecm integration,automated document generation,regulatory operations,and regulatory publishing

Docshifter operates in the It services and it consulting industry.

Docshifter's revenue is 11m - 100m

Docshifter has 11 - 50 employees.