Targeted Regulatory Writing offers flexible and efficient solutions to meet your regulatory and writing needs: Targeted to each stage of your product development and your product’s life cycle (drugs, medical devices and borderlines).
All documents are clear and well-written, designed to exceed your expectations. During document development, there is regular communication with the client (if requested) to ensure that all documents follow client preferences in terms of content and formatting.
Dedicated checklists per document are available to ensure high quality and full compliance with any applicable regulatory guidelines.
Save your own personal resources by means of strategic outsourcing. Let me support you with the creation/quality control of your documents and ask me whatever regulatory question might come up during the development of your product.