Meet Compliance and Improve Product Adoption

 

Learn More

Medical   |   Manufacturing   |   Cyber Security

Product Documentation and Training
for Medical Device & Regulated Industries

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 to success. If you lack the in-house resources to meet deadlines and compliance requirements, Novatek's outsourced technical writers can create instructions, manuals, tutorials, and online help.

 EU MDR

How Can We Help?

Product-Manager

Product Manager

Get the user-friendly product documentation and IFUs to successfully launch your product on time and improve product adoption.
Quality-Manager

Quality Manager

Meet compliance requirements and minimize company risk with accurate, up-to-date procedures and process documentation.
IT-Manager

IT Manager

Document your IT policies and procedures – and train your employees – to mitigate risk of cyber attacks.
Marketing-Manager

Marketing Manager

Increase product utility and sales revenue with customer training and documentation resources. 
Case-study-background

Documented standards + procedures for
ISO 13485, EU MDR, ISO 27001, and MDSAP compliance.

Get in Touch

Proven Expertise

For over 30 years, Novatek’s outsourced technical writers and instructional designers have reduced strain on manufacturers, producing materials that deliver on companies' needs for compliance and usability, while still staying on budget. Our team of experts ensures you'll have all the necessary documentation and training to:

  • Meet compliance
  • Support customers
  • Prepare for audits or inspections
  • Handle a serious incident

Case Studies