Creation and updating of the technical documentation for medical devices is time-consuming and expensive, but it is essential to achieve market approval. However, part of the work is wasted time. Regulatory requirements for the content of documents lead to redundancies of information in several documents. With Word/Excel/PDF files, manual copy & paste and a multitude of references is required. Maintaining these not only costs time, but sooner or later leads to inconsistencies. With digital software solutions, this is no longer necessary.

In this webinar, we will go through all phases of the creation of digital technical documentation:

1. Management of the product development process
2. Digital creation of documents with information units, e.g. in product development, risk management or clinical evaluation
3. Electronic review and approval process
4. Filing of the approved records and compilation of the submission file

We are looking forward to welcome you!