Technical Documentation and Training for
Medical Device & Regulated Industries
Meet compliance and improve product adoption
Product managers oversee complex product launch plans in the face of tight timelines, regulatory compliance requirements, and quickly evolving user needs. Product and process documentation are critical, but few companies have the in-house technical writing resources to deliver.
Novatek creates instructions, manuals, tutorials, and online help for:
- Users – to operate equipment and devices accurately and reliably
- Field engineers – to fix and maintain, so products are reliable and always available
- FDA regulators – to ensure that the device is safe and effective
- Sales people – to sell it
- Manufacturing & assembly – to ensure consistent quality
Novatek helps meet compliance and improve product adoption by:
- Proving ease of use through the creation of simplified user and technical documentation and training.
- Completing labeling requirement for achieving regulatory compliance faster.
- Improving usability for healthcare staff therefore enabling them to better focus on patient outcomes.