Training schedule 2022


The first morning will be devoted to the regulation of cosmetic products in Europe. The second morning will focus on the product information file and cosmetovigilance. 

2 Webinar mornings in January 

24 – 25 January 2022 at distance

Program and registration form


The first morning will cover the regulation of food supplements, bases to know. The second morning will provide an update on “health claims” regulation as well as current and future regulatory changes.

…in Europe

1st session in February 

24 – 25 February 2022 at distance

…in France

1st session in March 

7 – 8 March 2022 at distance

…in Europe

2nd sessionin September 

26 – 27 September 2022

Program and registration form

…in France

2nd session in October 

3 – 4 October 2022


Two mornings dedicated to the creation of your labels and packaging. What are the compulsory indications to be displayed on your packaging? What are the new requirements imposed by the AGEC Act in terms of consumer information, eco-design and waste management? What developments are still to come?

1st session in March 

10 – 11 March 2022 at distance

2nd session in October 

6 – 7 0ctober 2022

A morning to understand the regulation of herbal medicines (framework, monographs, procedures…), coupled with a second morning to talk about food supplements and their borderline products (DM, COS, MED, AGS): what are the constraints and opportunities, costs, and deadlines? Discussions on practical cases will conclude these two mornings.

2 Webinar morningsin March 

21 – 22 March 2022 at distance

« Health Communication : Which Health Communication for Food Supplements? »

Two mornings dedicated to health communication : « Which health communication for Food Supplements – Consumer tests, clinical studies, scientific publications – Valuing and highlighting the results ». 

1st session in April 

4 – 5 April 2022 at distance

2nd session in October 

17 – 18 October 2022


« Canadian Natural Health Products Regulation»

Two mornings dedicated to the regulation of NHPs in Canada: regulatory framework, labelling requirements, registration procedures, operators’ obligations…

1st session in April 

28 – 29 April 2022 at distance

2nd session in November 

7 – 8 November 2022


« Regulation of animal feed in the EU – Feed : What are the regulatory constraints and opportunities? »

Two mornings dedicated to animal nutrition : “Feed : What are the regulatory constraints and opportunities ? “. 

1st session in May 

19 – 20 May 2022 at distance

2nd session in December 

5 – 6 December 2022


« Manufacturing and distribution of medical devices : How to control them from a regulatory point of view ? What are the impacts of the new regulation ? »

This training course provides an overview of the regulatory framework for medical devices. It will enable you to know the steps and obligations required for the manufacturing and distribution of medical devices, know how to recognize the mandatory information on the labelling and the leaflet of a MD and to become aware of the transition periods granted by the MDR. 

1st session in June 

16 – 17 June 2022 at distance

2nd session in November 

21 – 22 November 2022


« Understanding and anticipating the controls of your food supplements by the administration»

Two mornings dedicated to the requirements for those placing products on the market and to controls carried out in the field: what are your obligations as a person responsible for placing products on the market? technical files, subcontracting contracts/contracting specifications, registration… How do the DDPP controls work? frequency, procedure, sanctions…

2 Webinar mornings in June 

27 – 28 June 2022 at distance




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