CROSS-SECTOR INNOVATIONS & LEGAL LOOPHOLES

Similar documents
COMMISSION OF THE EUROPEAN COMMUNITIES REPORT FROM THE COMMISSION TO THE COUNCIL AND THE EUROPEAN PARLIAMENT

GENERAL PRINCIPLES ON FLEXIBILITY OF WORDING FOR HEALTH CLAIMS

Presentation on Food Supplements. French practice. Stéphane Martin CEO ARPP/France. Bucharest, 22 of April of 2016

The Italian approach to probiotics

Claims about health in ads for e-cigarettes. CAP and BCAP s regulatory statement

Discussion Paper on NUTRITION CLAIMS AND FUNCTIONAL CLAIMS

Nutrition and Health Claims Regulation (EC) Nº 1924/2006 on Nutrition and Health Claims made on foods

ACS Submission: Consultation on the advertising of electronic cigarettes

MEDICINES, MEDICAL DEVICES, TREATMENTS AND HEALTH

Roadmap to review the Nutrition and Health Claims legislation expression of interest to contribute to the upcoming external study

EUROPEAN COMMISSION SUMMARY REPORT OF THE STANDING COMMITTEE ON THE FOOD CHAIN AND ANIMAL HEALTH HELD IN BRUSSELS ON 13 JUNE 2014

EUROPEAN COMMISSION HEALTH AND FOOD SAFETY DIRECTORATE-GENERAL. PHARMACEUTICAL COMMITTEE 21 October 2015

Industry and globalisation of herbal medicines

SUMMARY REPORT OF THE STANDING COMMITTEE ON THE FOOD CHAIN AND ANIMAL HEALTH HELD IN BRUSSELS ON 10 DECEMBER 2012 (Section General Food Law)

A Seminar on EU Regulations on Food Labelling

(Text with EEA relevance)

COMMISSION DELEGATED REGULATION (EU).../... of XXX

AGREEMENT ON COMMON PRINCIPLES AND RULES OF CIRCULATION OF MEDICINAL PRODUCTS WITHIN THE EURASIAN ECONOMIC UNION. (Moscow, 23 December 2014)

Medical Devices. SOUTH AFRICA Bowman Gilfillan

AIDS LAW PROJECT/TREATMENT ACTION CAMPAIGN: SUBMISSION ON THE REGULATIONS RELATING TO THE LABELLING AND ADVERTISING OF FOODSTUFFS 1

on the advertising of medicinal products for human use

The Food for Specific Groups (Information and Compositional Requirements) (England) Regulations 2016

Determining Whether A Dietary Supplement Study Requires an Investigational New Drug (IND)

(OJ L 276, , p. 40)

COUNCIL OF THE EUROPEAN UNION. Brussels, 7 September 2009 (OR. en) 11261/09 Interinstitutional File: 2008/0002 (COD) DENLEG 51 CODEC 893

Plain Packaging and Intellectual Property Rights. Cheng Tan, Head of Trade Marks

Aligning a Product s Marketing, Regulatory and IP Plans

Healthy Living. with Arbonne

Introduction on the Regulations on Imported Nutrition Supplements of the Republic of China

Food Legislation. Janet Worrell July 2014

Dagmar Roth-Behrendt Vice-President of the European Parliament

References to people who are obese in weight loss advertising

European Union legislation on Food additives, Food enzymes, Extractions solvents and Food flavourings

European Commission request to the European Food Safety Authority for scientific advice on:


Policy Options for the Regulation of Electronic Cigarettes

COMMISSION OF THE EUROPEAN COMMUNITIES. Proposal for a DIRECTIVE OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL

IPPT , ECJ, Commission v Germany (garlic extract powder capsule) No medicinal product by function

CNHC Guidance on The Cancer Act (Please note this does not constitute legal advice)

JUDGMENT OF THE COURT (First Chamber) 15 November 2007 * ACTION under Article 226 EC for failure to fulfil obligations, brought on 19 August 2005,

FDA Regulation of Claims on Dietary Supplement and Food Products

C 178/2 Official Journal of the European Union

Bill C-51 and Natural Health Products - The Facts

CIAA COMMENTS ON DG SANCO DISCUSSION PAPER ON NUTRITIONAL AND FUNCTIONAL CLAIMS

15 years of the European Union s Food Supplement Directive

The Uses and Abuses of Negative Claims

COUNCIL OF THE EUROPEAN UNION. Brussels, 15 November 2005 (OR. en) 9858/05 Interinstitutional File: 2003/0165 (COD) DENLEG 25 SAN 105 CODEC 481 OC 382

CHAPTER 34 LINN COUNTY DRUG PARAPHERNALIA ORDINANCE

IMPORTANT DISCLAIMER. Note

Health Claims and Botanicals: How to Proceed with European Harmonisation?

Understanding the New Access to Cannabis for Medical Purposes Regulations

The Nutrition (Amendment) (EU Exit) Regulations 2018

EUROPEAN COMMISSION SUMMARY REPORT OF THE STANDING COMMITTEE ON PLANTS, ANIMALS, FOOD AND FEED HELD IN BRUSSELS ON 07 MARCH 2017

Permitted Cannabis Marketing Activities

What Regulators and Other Attorneys Will Not Tell You About FDA, FTC, and Class Action Lawsuits Venable LLP

New Novel Food Regulation

Third Seminar on Bad Faith TM Filings. Ignacio de Medrano Caballero, OHIM TM5, Tokyo, 1 March 2016

Cannabis Legalization August 22, Ministry of Attorney General Ministry of Finance

Regulation of Foods Containing Probiotics - Codex Alimentarius, Japan, European Union and India

Guidelines to Commission Regulation (EU) No 655/2013. laying down common criteria for the justification of claims used

ADVANCED TECHNOLOGY CONFERENCE. The definition of a cosmeceutical. Anthony C. Dweck Research Director, Peter Black Medicare Ltd.

Permitted Cannabis Marketing Activities

PROMOTION AND SALE OF IVDS IN EU

ENERGIZE REVITALIZE DETOXIFY

Kansas Sheriffs Association PO Box 1122 Pittsburg, KS (620)

Recent Developments in Regulation of Nutrition and Health Claims

CED GUIDELINES TO INTERPRET AND IMPLEMENT COUNCIL DIRECTIVE 2011/84/EU ON TOOTH WHITENING PRODUCTS

Dutch consumers association with members Since 1953 Mission: to defend consumers rights and help them make informed choices

Ornsurang Teerawat

Republika e Kosovës Republika Kosovo - Republic of Kosovo Kuvendi - Skupština - Assembly

Getting Your Ingredient to Market: Understanding Your Regulatory Options Venable LLP

COMMISSION OF THE EUROPEAN COMMUNITIES REPORT FROM THE COMMISSION TO THE EUROPEAN PARLIAMENT AND THE COUNCIL

Update from the European Commission s Working Group meeting on health claims, 31 March 2015

(Information) INFORMATION FROM EUROPEAN UNION INSTITUTIONS, BODIES, OFFICES AND AGENCIES EUROPEAN COMMISSION

Claims related to Whole Grains

Medical Devices. BARBADOS Clarke Gittens Farmer

SCIENTIFIC OPINION. EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA) 2. European Food Safety Authority (EFSA), Parma, Italy

Guideline on Health Food Exportation to China

M I L L E R T H O M S O N LLP Barristers & Solicitors, Patent & Trade Mark Agents

The legal basis of this draft Regulation is Art. 11 (4) of Regulation (EC) No. 882/2204.

Food additives and nutrient sources added to food: developments since the creation of EFSA

Standards for Professional Conduct In The Practice of Dentistry

Secretary of the Senate. Chief Clerk of the Assembly. Private Secretary of the Governor

Emanuela Turla Scientific Officer Nutrition Unit - EFSA

British American Tobacco Snus Marketing Standards

GUIDELINES FOR USE OF NUTRITION AND HEALTH CLAIMS

COMMISSION OF THE EUROPEAN COMMUNITIES. Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL

Guidelines c o n n e c t t o t h e w o r l d o f d a i r y

Food additives. FAO guidelines on the structure and content of the document called "Chemical and Technical Assessment (CTA)" Rome, February 2003

UKAS Guidance on the Application of ISO/IEC Dealing with Expressions of Opinions and Interpretations

Presentation: Philip G. Hampton, II Haynes and Boone, LLP (202) September 14, 2017

JOSEFIEN VENDRIK, QUALITY MANAGER IRENE JONGENELEN, COÖRDINATOR CLINICAL SUPPLIES MANAGEMENT/ SENIOR CLINICAL STUDY MANAGER

QUESTIONS AND ANSWERS

Response to the European Commission Discussion Paper on the setting of maximum and minimum amounts for vitamins and minerals in foodstuffs

Genetically Modified Organism (GMO) Legislation and Litigation: Challenges and Opportunities

Regulatory and Investment Framework for Traditional Chinese Medicine in Hong Kong

STANDING COMMITTEE ON THE FOOD CHAIN AND ANIMAL HEALTH SECTION ON GENERAL FOOD LAW. Summary Record of Meeting of 30 April 2012

perpetuate -- and perhaps even intensify -- that controversy. 1 On July 18th, the Fifth Circuit affirmed FDA s longstanding position that

SECOND MEDICAL USE CLAIMS

An update on the regulatory framework for labelling across the EU Dr David Jukes Department of Food and Nutritional Sciences University of Reading

Transcription:

CROSS-SECTOR INNOVATIONS & LEGAL LOOPHOLES Dutch Life Sciences Conference Leiden, 24 November 2016 Karin Verzijden www.axonlawyers.com

Agenda Warming-up: testing your knowledge on product qualification Legal framework for distinction between various types of life sciences products Legal consequences on product qualification Take home 2

Product qualification (1) 3

Product qualification (2) Decision of Dutch Supreme Court 11 November 2016 ECLI:NL:HR:2016:2560 4

Product qualification (3) Lucovitaal puur en groen Improves the digestion of food containing gluten and lactose

Product qualification (4) NutriBullet blender Pulverizes food at cell level, enabling the body to easily absorb nutrients such as vitamins, mineral and fibers Testimonial as to positive effects by former cancer patient 6

Product qualification (5) XL-S Medical aangeprezen door René Froger 7

Legal framework (1) Product definitions Medicinal product: any product aimed at curing, preventing or diagnosing a disease Article 1.2 Medicinal Products Directive 2001/83 Article 1.1 (b) Dutch Medicinal Product Act Food product: any product intended to be ingested by humans Article 2 General Food Law Regulation 178/2002 Article 1 (b) Dutch Commodities Act

Legal framework (2) Interpretation of product definitions As to medicinal products, the following criteria were developed in case law as of the 80-ies and are still applied nowadays: Distinction between medicinal products by presentation or by function (aandieningscriterium vs. toedieningscriterium) As to the distinction between medicinal product and any other product, art. 2.2 Medicinal Products Directive and art. 1 (6) Dutch Act on Medicinal Products provide: When in doubt, rules relating to medicinal products shall prevail

Legal framework (3) How about advertising? It is prohibited to advertise medicinal products without having a market authorization Article 6 Medicinal Products Directive Article 84 Dutch Medicinal Product Act Article 4 Dutch Advertising Code Medicinal Products For advertising food products, it is permitted to use authorized nutrition & health claims, but it is prohibited to use medical claims Recital 3 Claims Regulation 1924/2006 + NVWA guidance # 79 Article 7.1 (b) Labelling Regulation 1169/2011

Legal framework (4) What are medical claims exactly? Chardonnay grape seeds offer inflammation mitigating advantages Aloë Vera benefits digestion or to calm down the bowl system Black cumic seeds boost the immune system Dutch Advertising Code Committee 23 August 2016 ruling on Rain Core and Rain Soul seed mixes. Bottom line: communications claiming that advertised products improve health problems imply that these products have a medical effect. Thin line between non-authorized medical claims and authorized disease reduction claims!

Legal framework (5) What should be understood by advertising? Depending on source, notion can be pretty broad and not only factual. According to Dutch Advertising Code advertising covers any public and /or systematic direct or indirect recommendation of goods, services or views for the benefit of an advertiser, whether or not using third parties Covers so-called influencers Social Media Code (1 January 2014) Can cover client reviews when circulated systematically

Case law (1) Medicinal product by presentation ECJ van Bennekom (227/82) Facts Large quantity of (multi) vitamin preparations traded by Dutch national van Bennekom was seized > Medicinal Products Supply Act. Preparations in pharmaceutical form and highly concentrated. Van Bennekom did not meet registrations & authorization requirements. According to him, products were foodstuffs, not medicinal products. Ruling Concept of presentation broadly construed > consumer protection. No benchmark for vitamins to qualify as a medicinal product > evaluation on case-by-case basis. As long as there is no full harmonization in place, MS may apply their national legislation requiring market authorisation for such products.

Case law (2) Medicinal product by function (ECJ Hecht-Pharma, case C-140/07) Facts Hecht Pharma was marketing a fermented red rice product in the form of capsules presented as food supplements. Further marketing in Germany was prohibited, as it contained significant levels of monalin k > inhibitor of cholesterol synthesis. In sum, the product was considered to be a medicinal product by function, for which no marketing authorisation had been obtained. Ruling Regarding a medicinal product by function, it should be scientifically established that it is capable of restoring / correcting / modifying physiological functions of the human body assessment case-by-case!

Case law (3) Melatonine based food supplements (The Hague Court 1 June 2016) Facts Dutch Health Inspectorate (IGZ) had announced enforcement measures regarding various melatonin based food supplement containing > 0,3 mg melatonin marketed by different manufacturers. Central announcement of enforcement action via health products association NPN. Ruling Prior to enforcement measures, IGZ should motivate why a particular product qualifies as a medicinal product. Each product should be assessed on an individual basis, applying the criteria developed in standing EU case law (Van Bennekom, Hecht i.a.).

Case law (4) What are functional foods? Appeal Court The Hague 7 June 2016 Facts Both Unilever and Ablynx had obtained a license from Brussels University (VUB) under certain antibodies patents owned by VUB. License Unilever food products, license Ablynx medicinal products. Under its license, Unilever developed so-called functional foods having certain beneficial effects against infections caused by the rota-virus. Ablynx claimed Unilever thereby had operated outside its licensed field. Ruling Unilever s license was directed at non-pharmaceutical products. It can target general health benefits but not specific pathogens.

Case law (5) Food product = medical device Dutch Advertising Code Cie. 2 June 2016 Facts Dutch singer René Froger claims he lost 8 kg. thanks to XL-S Medical. According to claimant, such claims for food products are prohibited according to art. 12.b Claims Regulation 1924/2006. Based on NVWA website info, testimonials re. before and after are prohibited. Ruling XL-S is medical device food law not applicable. Applicable framework is Medical Device Code (MDC). Art. 7.2 MDC prohibits stating the amount of weight loss / time unit, but allows stating achieved results.

Take home (1) How to obtain pre-market clearance for communication on health products? Take guidance from Advertising Code Health Products (Code Aanprijzing gezondheidsproducten), applicable to products having a pharmaceutical form and a health related primary function, however without being medicinal products Commodities Act (Warenwet) Obtain approval from KOAG / KAG Keuringsraad, whom actively evaluates claims and provides endorsements

Take home (2) How to deal with enforcement measures? In case of violation of applicable laws, usually IGZ and NVWA do not fine immediately, but initially share their intention to do so and offer the opportunity to respond. Buy some time by claiming an extension for response. Carefully consider if claims made by enforcement authorities are factually & scientifically correct and legally enforceable.

Conclusions Begin with the end in mind: what type of product will you be marketing? Prevention is better than curing: know the rules! Pay careful attention to the grey area of borderline products. If and when confronted with enforcement measures..