Solution

Technical Day

You have a concept to validate, a strategic question to answer, a new direction to explore or you want to understand the requirements applicable to your product before committing your teams. The Technical Day is designed for exactly that.

In a single day, in a small group, you review all the parameters that will determine the success of your project: regulatory, technical, clinical, quality and strategic.

What you get :

  • A clear picture of the regulatory, technical, quality, clinical and strategic considerations to anticipate
  • An assessment of the impact on your timeline and resources
  • Concrete recommendations to manage financial and business risks
  • The elements needed to decide with confidence: proceed, adapt or pivot

For whom?

Executives, R&D or innovation project leaders who want to validate the feasibility of a project or resolve a strategic question before committing significant resources.

How does the Day unfold?

1.

Pre-session scoping

Preparatory exchange to understand your project, objectives and constraints. Definition of the day’s programme.

2.

Preparation

Analysis of the elements provided and preparation of evaluation frameworks by One Health Compliance.

3.

The day

Structured review of all key parameters: regulation, product qualification, technical and clinical requirements, impact on timeline and resources.

4.

Q&A and discussion

Dedicated time for your specific questions, alternative scenarios and priority decisions.

5.

Written debrief

A structured summary document delivered within a few days: key points, concrete recommendations and prioritised decision elements.

6.

Follow-up

A post-debrief exchange to answer questions raised on reading the document.

FAQ

  • What type of project is the Technical Day suited to?

    The Technical Day adapts to a wide range of situations: a concept at the idea stage, an existing product for which you are considering a new indication or market, or a strategic question about the relevance of a regulatory approach or understanding the ISO 13485 requirements applicable to your activity as a medical sector service provider or supplier. For example: a company marketing equine care products wondering about the steps needed for a first clinical study in human health, or a wellness products company wanting to understand whether a medical device approach would be strategically relevant.

  • How many people can participate?

    The Technical Day is designed for a small group, ideally 1 to 3 people. This format allows for in-depth exchanges and enables the programme to be adapted in real time to your questions.

  • What do I need to prepare beforehand?

    Very little on your side by design. A preparatory exchange and a few elements of context about your project are sufficient. One Health Compliance takes care of structuring and preparing the content.

  • What form does the debrief take?

    A clear and actionable written document is delivered within a few days of the session. It covers the key points discussed, concrete recommendations and the elements needed to decide with confidence: proceed, adapt or pivot.

  • Can the Technical Day lead to a longer engagement?

    Yes, and this is often the case. The Technical Day may reveal that a Project Audit is needed, or identify concrete actions that One Health Compliance can support. But it is also designed to be valuable in its own right, with no obligation to continue.

  • Is the Technical Day held in person or remotely?

    Both formats are possible, depending on your preferences and location. One Health Compliance operates in France and internationally.