Documentation is essential to good science, and that’s especially true for companies developing new science and technology products in biologics, pharmaceuticals, medical devices, and enterprise software. Each stage your product and business goes through will require different types of documents and records, and Doxpub’s services can meet your needs from lab and engineering to trial and market. We work onsite in the 206 and 425 area codes of Washington State, USA, and our remote services can be delivered globally.
Areas of expertise:
- Laboratory
- Clinical
- Engineering
- Manufacturing
- Quality
- Regulatory
- Intellectual Property
Service offerings:
- Documents and Records
Our document and record services focus on preparing and coordinating your documents. We write, edit, format, design, verify, publish, scan, and archive documents like policies, procedures, forms, protocols, reports, plans, specifications, templates, controlled docs, CTD submissions, TMFs, DMFs, BPRs, MBRs, DMRs, DHFs, spreadsheets, presentations, and help files. We also coordinate the review and approval of documents amongst your team members, and we support your audit and due diligence activities. - Information Systems
Years of experience have given us in-house expertise in the information systems that generate and store your electronic records and signatures. We analyze, design, migrate, validate, and administer systems for handwritten, printed, & electronic records including LIMS, SDMS, CTMS, File Sytem Auditor, Author-IT, SharePoint, file servers, FTP, Pipeline Exchange, wikis, SQL, PACS/DICOM, Part 11 and GAMP systems. - Training
We train groups and individuals on good documentation practices, lab notebooks, doc control, records mgmt, Microsoft Word, Excel, Visio, PowerPoint, SharePoint, Adobe Acrobat, ISI PharmaReady ToolBox, Mission3, NextDocs
Contact us if you have any questions about good documentation practices or Doxpub’s products and services.