EryonStudio, healthcare motion design studio
Our films, the method, the communication kit and the process, from idea to final version.
A medical device explainer video shows what your product does and how to use it: how it works, exploded view, instructions for use, training. For product managers, regulatory affairs and training managers, EryonStudio, Eryon's video studio in Lille, France, delivers a first version within a few days. Every line refers to the instructions for use, the intended purpose or its reference, with the exact passage.
Depending on the audience and where it is shown, the same animation serves to explain, train or present, with the rules specific to each use.
What the device does, for whom and how: from the overview to the internal mechanism, in the words of the instructions for use and the intended purpose. Nothing on screen suggests a use that the conformity assessment has not covered.
Cap, needle cover, syringe, spring: in 3D animation, each part comes away, is named and returns to its place. The exploded view shows the inside of the finished product. A single-use prefilled auto-injector forms one product with its medicine: its video then follows medicine rules (marketing authorisation, SmPC and, for advertising, ANSM approval). Images commit you as much as text, and every diagram stays labelled as an illustration.
The steps in the instructions for use, in order: prepare, use, remove, dispose of. The procedure is shown at the user's pace, and every warning in the instructions appears at the moment it matters.
For patients who use the device at home: the information in the instructions for use and the product's characteristics, in images and plain words, given after prescription or fitting. Without promotional claims, it is not classified as advertising by the ANSM, the French regulator.
Demonstration of use, maintenance, reprocessing of the device: the video trains nurses, pharmacists or theatre teams. Consistent with the instructions for use and without claims about the product's advantages, it remains a correct-use tool.
To present the device to healthcare professionals: claimed intended purpose and performance, class, notified body number, statements legible on screen. It is an advertisement: we write it as such, ready for your review and, if the device requires it in France, for the ANSM authorisation.
This film explains a device without selling it: its principle and its limits, in plain words, with no name or brand. For your product, the method is the same, starting from your instructions for use and your intended purpose.
A well-referenced animation can be reused at every stage of the device's life, from launch to updates of the instructions for use.
A launch: presenting the device to healthcare professionals, at congresses or on sales calls, with its mandatory statements.
Training: teaching clinicians to prepare, use, maintain and reprocess the device, in hospital or in the community.
A handover to the patient: the correct-use video, given after prescription or fitting, turns the instructions for use into images.
An update to the instructions for use: the film, cut step by step, is revised where the instructions change.
A new market: the video in that market's language, every line tied to that country's instructions for use, and local advertising rules checked at scoping.
For a device, the first sources are your own: instructions for use, intended purpose, labelling, then the scientific literature. Every line of the script is tied to them, with the page and the exact passage, before the first frame.
Objective, audience, where the video will be shown, available references and regulatory points to watch.
Every line is tied to a reference, with its page and the exact passage that supports it.
Motion design and medical animation, with AI assisting part of the production. Diagrams remain illustrations.
An automated check finds every passage, word for word, on the page cited; two independent AI-assisted audits then re-check a sample in the documents; your review committee, or your MLR review in a pharmaceutical company, approves the final version.
The film comes with its broadcast files and the file that justifies it, ready for your approval process and, if the advertisement requires it in France, for the authorisation application to the ANSM.
Landscape for your website, YouTube and the training room; portrait, square or 4:5 for social media.
SRT file and full text: accessibility, viewing without sound and search visibility for the page that hosts the film.
Every line, its reference, its page and the exact passage, ready for your internal review.
The full list, in order of appearance, with links to the public sources.
Short excerpts, stills, a poster or slides, depending on your channels. Quoted with the final version.
The languages you choose: every translated line keeps its source and exact passage, and the rules of the country where the video is shown are checked at scoping.
In France, a video that promotes the prescription, sale or use of a device is an advertisement (Article L.5213-1 of the French Public Health Code): objective, with the notified body number (Article L.5213-2), and suggesting no use outside the intended purpose (Regulation (EU) 2017/745, Article 7). For the devices listed in the amended ministerial order of 24 September 2012, the ANSM authorises in advance advertising aimed at healthcare professionals and, to the public, advertising for dermal fillers (Article L.5213-4). To the public, a device covered by national health insurance can only be promoted if it is class I or IIa (Article L.5213-3). A correct-use video faithful to the instructions for use, without claims, is not advertising according to the ANSM, and no video replaces the instructions for use. We write within this framework; the decision to release it remains yours.