Expert FrameMaker Authoring Services: Structured and Unstructured Solutions at Affordable Rates
Professional technical documentation that meets S1000D, ATA Spec 2200, FDA, and ISO 9001 standards, and more
Professional technical documentation is more than just words on a page—it’s the foundation of regulatory compliance, operational efficiency, and customer success. Whether you’re navigating S1000D requirements in aerospace and defense, meeting FDA submission standards for pharmaceutical and medical devices, or ensuring ISO 13485 compliance for quality management systems, the complexity of modern documentation demands expertise that understands both the technical requirements and the authoring tools that deliver results efficiently.
Our structured and unstructured FrameMaker authoring services specialize in the most demanding regulated industries, including aerospace and defense, pharmaceutical and medical devices, clinical documentation improvement, healthcare systems, manufacturing quality management, and defense contracting. We have deep expertise in industry-specific documentation standards such as S1000D for aerospace technical publications, ATA Spec 2200 and iSpec 2200 for aviation maintenance, FDA 21 CFR Part 11 for pharmaceutical and medical device submissions, ISO 9001 and ISO 13485 for quality management systems, and DITA-based structured content for multi-channel publishing.
From data modules and Interactive Electronic Technical Publications (IETP) to Clinical Evaluation Reports (CERs) and Standard Operating Procedures (SOPs), we deliver documentation that meets the stringent requirements of global regulators and industry standards bodies.
What sets us apart is our unique combination of affordable pricing—typically 30-40% below industry standard rates—and uncompromising professional quality backed by decades of experience in regulated documentation environments. We understand that compliance deadlines are non-negotiable, budgets are constrained, and documentation quality directly impacts your ability to bring products to market, maintain certifications, and ensure operational safety. Our structured authoring approach using FrameMaker enables modular, reusable content that adapts as regulations evolve, reducing long-term maintenance costs while ensuring consistency across your entire documentation portfolio. Whether you need a complete documentation system developed from scratch, legacy content migrated to modern standards, or expert support during critical regulatory submissions, we provide the expertise, responsiveness, and affordability that growing organizations require.
Request Your Free Review
Regulatory Deadline Approaching? Get Expert Documentation Support Now QMSR, IVDR, S1000D, FDA submissions, and more
We deliver compliant documentation on your schedule
FrameMaker Regulatory Documentation Services
Structured FrameMaker Authoring
- DITA/XML authoring and conversion
- Unstructured to structured conversions
- S1000D-compliant documentation
- ATA iSpec 2200 technical publications
- FDA regulatory documentation
- EDD development and template customization
Unstructured FrameMaker Authoring
- Technical manuals and user guides
- Product documentation
- Training materials
- Marketing collateral with technical specifications
🔔 REGULATORY ALERT: QMSR Compliance Deadline – 3.5 Months Away!
⚠️ Medical device manufacturers: February 2, 2026 is approaching fast. The FDA’s Quality Management System Regulation (QMSR) requires transition from QSR to ISO 13485:2016-aligned systems. This is the biggest quality system change in 25+ years.
📋 KEY REQUIREMENTS: → ISO 13485:2016-compliant QMS documentation → Updated lifecycle management documentation → New document control procedures → ISO 14971-aligned risk management docs
⏱️ TIMELINE: 6-12 months needed for comprehensive overhaul
💡 START NOW: Gap analysis of QSR vs ISO 13485 requirements
We specialize in QMSR compliance documentation using structured authoring that saves 30-40% development time. FREE compliance review included
Source: https://www.fda.gov/medical-devices
Industry Specialization
- Aerospace and Defense (S1000D expertise)
- Aviation (ATA Spec 2200)
- Medical Devices and Pharmaceuticals (FDA compliance)
- Manufacturing (ISO 9001 documentation)
Why Work With Us?
- Transparent, Affordable Pricing at 30-50% below industry standard rates
- Flat fee, project-based versus hourly options available
- Free Compliance Review to ensure best practices documentation
Knowledgeable and Professional
- Exceptional Quality and deep industry knowledge for alll standards covered
- Wide range of documentation expertise to best suit your requirements.
- Free Compliance Review to ensure best practices documentation.
Documentation Gap Analysis
Schedule a Free Compliance Documentation Review
Discover gaps in your current documentation and planned submissions. Get expert guidance on meeting your regulatory requirements
No obligation review