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Training schedule 2022

DOUBLE WEBINAR MORNINGS

 

« Regulation of herbal medicines (1st morning) + Food supplement border products (2nd morning)»

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 mornings in March 

15 – 16 September 2022 at distance

PROGRAM AND REGISTRATION FORM

 

« Food supplements regulation… »

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

2nd sessionin September 

26 – 27 September 2022

Program and registration form

…in France

2nd session in October 

3 – 4 October 2022

Program and registration form

 

« Labelling of food supplements (1st morning) – AGEC law (2nd morning)»

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?

2nd session in October 

6 – 7 0ctober 2022

Program and registration form

 

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

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

2nd session in October 

17 – 18 October 2022

PROGRAM AND REGISTRATION FORM

 

« Canadian Natural Health Products Regulation»

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

2nd session in November 

7 – 8 November 2022

PROGRAM AND REGISTRATION FORM

 

« 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. 

2nd session in November 

21 – 22 November 2022

PROGRAM AND REGISTRATION FORM

 

« 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 ? “. 

2nd session in December 

5 – 6 December 2022

PROGRAM AND REGISTRATION FORM

 

« Regulation of cosmetic products in Europe and its latest news (endocrine disruptors, AGEC law, allergen labelling…) »

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

 

« 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 morningsin June 

27 – 28 June 2022 at distance

PROGRAM AND REGISTRATION FORM

 

 

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