Legal Requirements for the Control of Contaminants in Herbal Medicinal Products and Related Areas

Similar documents
QUALITY OF HERBAL MEDICINAL PRODUCTS: PRESENT REQUIREMENTS

ASEAN GUIDELINES ON LIMITS OF CONTAMINANTS FOR TRADITIONAL MEDICINES (TM) AND HEALTH SUPPLEMENTS (HS)

ANNEX III ASEAN GUIDELINES ON LIMITS OF CONTAMINANTS FOR TRADITIONAL MEDICINES

Risk Management of Contaminants in Herbal Substances and Herbal Preparations

(notified under document C(2017) 4975) (Only the English text is authentic)

DRS 169 RWANDA STANDARD. Chilli oil Specification. Second edition mm-dd. Reference number DRS 169:2017

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

DRAFT EAST AFRICAN STANDARD

TANZANIA BUREAU OF STANDARDS

Formulation stability studies. 9.1 OBJECTIVE To monitor the stability of the developed herbal formulations using the limited and specific methods.

Sweetpotato puree - specification

Product Data Sheet Hemp Oil 3% CBD. 1. General information. Best before: 06 / Product information: Appearance Ingredients CBD oil

Good pharmacopoeial practices: Chapter on monographs on herbal medicines

TANZANIA BUREAU OF STANDARDS

DRAFT UGANDA STANDARD

SANCO/10616/2009 rev. 7 ( )

DRAFT EAST AFRICAN STANDARD

EUROPEAN COMMISSION SUMMARY REPORT OF THE STANDING COMMITTEE ON PLANTS, ANIMALS, FOOD AND FEED HELD IN BRUSSELS ON 23 SEPTEMBER 2015

EAST AFRICAN STANDARD

QUALITY OF HERBAL REMEDIES

TANZANIA BUREAU OF STANDARDS

DUS 872 UGANDA STANDARD. Second Edition 2018-mm-dd. Fermented (non-alcoholic) cereal beverages Specification. Reference number DUS 872: 2018

The regulatory landscape. The now and the not yet

Discussion at the HMPC January March Draft agreed by Quality Working Party April Adoption by CHMP for release for consultation 26 May 2005

Safety Assessment of Paprika Extract EXS0570IND. Contact person(s): Céline Burgaud; Pharmanager Ingredients Céline Pozza, Pharmanager development

Scientific and Regulatory Basis for Development, Quality Assurance and Marketing Authorisation

FINAL DRAFT EAST AFRICAN STANDARD

DRS 125 RWANDA STANDARD. Fresh tofu Specification. Second edition mm-dd. Reference number DRS 125: 2018

REGIONAL STANDARD 1: DRAFT CASSAVA FLOUR - Specifications. Latest edition October 1, Reference number CARSPS 1: 2017

Regulatory changes and challenges in relation to cocoa

TANZANIA BUREAU OF STANDARDS

NORTHERN CORRIDORSTANDARD NC 4:2018. Roasted Macadamia Specification

Discussion by HMPC Drafting Group on Quality September Start of public consultation 15 February 2013

DRS RWANDA STANDARD. Spirulina products Specification. Part 1: Ground spirulina. First edition mm-dd. Reference number DRS 359-1: 2017

REGULATION concerning Marketing Authorisations for Natural Medicinal Products and Registration of Traditional Herbal Medicinal Products, No. 142/2011.

All Member States were represented except Cyprus and Lithuania.

Public Assessment Report Scientific discussion

H e r b a l M e dicines' Q U A L I T Y M ANUAL. I. Introduction

US EAS 801 UGANDA STANDARD. First Edition Soya protein products Specification. Reference number US EAS 801: 2014

Guideline on quality of herbal medicinal products 1 /traditional herbal medicinal products

ON FOOD SAFETY. April Paola Testori Coggi Directorate D/Food Safety DG SANCO European Commission

DRAFT EAST AFRICAN STANDARD

DRAFT UGANDA STANDARD

As extraction is done by critical CO 2

Final. Organisations and/or individuals. 1 Association of the European Self-Medication Industry (AESGP) 2 European Herb Growers Association (EUROPAM)

Guideline on quality of herbal medicinal products 2 /traditional herbal medicinal products

Development of risk-based standard on aflatoxin in peanuts

INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE

Results of border checks carried out by the EU Member States and Norway on imports of feed and food of non-animal origin subject to increased level

(notified under document C(2017) 7418) (Only the English text is authentic)

MEDICNES CONTROL AGENCY GUIDELINE FOR REGISTRATION OF HERBAL MEDICINAL PRODUCTS IN THE GAMBIA

Public Assessment Report Scientific discussion

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

COMMISSION REGULATION (EU) No /.. of XXX. amending Regulation (EC) No 1881/2006 as regards maximum levels of lead in certain foodstuffs

Ornsurang Teerawat

From the Ministry of Food, Agriculture and Livestock: TURKISH FOOD CODEX COMMUNIQUÉ ON ICED PRODUCTS (Draft 2017/.)

Overview of European Legislation on Food Contaminants. Dr Iona Pratt, Food Safety Authority of Ireland

KENYA STANDARD KS 2431: 2018 ICS Garlic paste Specification

Setting of new MRLs for fluxapyroxad (BAS 700 F) in various commodities of plant and animal origin 1

TECHNICAL REPORT OF EFSA. List of guidance, guidelines and working documents developed or in use by EFSA 1

Technical Specifications for the manufacture of: CANNED BEEF

U.S. Requirements for Dietary Supplement Ingredients and USP <2232> Elemental Impurities Is Your Company Ready for Implementation?

Public Assessment Report Scientific discussion

Draft of Sanitation Standards for General Foods

Evaluation of active substances in plant protection products Residues Anja Friel European Food Safetey Authority, Parma/ Italy

General Chapter/Section: <232> Elemental Impurities - Limits Expert Committee(s): General Chapters Chemical Analysis No.

INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICALS FOR HUMAN USE

COMMISSION STAFF WORKING DOCUMENT 1. Review report for the active substance Copper compounds

EUROPEAN COMMISSION DIRECTORATE-GENERAL FOR HEALTH AND FOOD SAFETY

REASONED OPINION. European Food Safety Authority 2, 3. European Food Safety Authority (EFSA), Parma, Italy

Increased checks on import of food of non-animal origin. Overview Controls carried out by the EU Member States. Food Safety

Dietary exposure assessment in the Slovak Republic

Organic Camelina Seed Virgin Oil

CBD CAPSULE (5MG) DESCRIPTION HempFlax s CBD capsule is made of a decarboxylated supercritical CO 2 GENERAL INFORMATION

232 ELEMENTAL IMPURITIES LIMITS

DIRECTIVE 2004/24/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL. of 31 March 2004

DRAFT TANZANIA STANDARD

EUROPEAN COMMISSION ENTERPRISE AND INDUSTRY DIRECTORATE-GENERAL. EudraLex The Rules Governing Medicinal Products in the European Union

Heavy metals, mycotoxins and pesticides in herbal drugs and extracts. Dr. Michael Schwarz PhytoLab GmbH & Co. KG

STANDARD FOR PROCESSED TOMATO CONCENTRATES CODEX STAN * Adopted in Revised in 2007, Amended in 2013.

COMMISSION REGULATION (EU)

KENYA STANDARD DKS Moringa leaf products Specification

Guideline on the use of the CTD format in the preparation of a registration application for traditional herbal medicinal products 1

The National Food Administration's Regulations on Certain Foreign Substances in Food 1

Practical guidance for applicants on the submission of applications on food additives, food enzymes and food flavourings

EUROPEAN COMMISSION HEALTH & CONSUMER PROTECTION DIRECTORATE-GENERAL

EUROPEAN COMMISSION DIRECTORATE-GENERAL FOR HEALTH AND FOOD SAFETY

TANZANIA BUREAU OF STANDARDS

(notified under document C(2017) 8431) (Only the English text is authentic)

Questions & answers on quality of herbal medicinal products/traditional herbal medicinal products 1

Test Results Standard. Appearance Light yellow, fine powder Matches std. Odour Characteristic Matches std. Taste Characteristic Matches std

General concepts in the Ph. Eur.: theory and rationale

Applying Risk Assessment Outcomes to Establish Food Standards

Discussion by HMPC Drafting Group on Quality February Start of public consultation 27 June 2012

Public Assessment Report Scientific discussion. Ginsana, soft capsule. Asp.no.:

(Text with EEA relevance)

COMMISSION STAFF WORKING DOCUMENT

European Medicines Agency Inspections

Organisations and/or individuals

Official Journal of the European Union. (Non-legislative acts) REGULATIONS

Transcription:

Legal Requirements for the Control of Contaminants in Herbal Medicinal Products and Related Areas AOAC International Workshop Erlangen, 11 October 2011 Dr. Barbara Steinhoff Contents Heavy metals Microorganisms Mycotoxins Polycyclic aromatic hydrocarbons Plant protection products Maximum residue limits Approval/ authorisation of active substances/products Integrated pest management 2 1

Heavy Metals: European Pharmacopoeia Monograph Herbal drugs (draft Extracts ) Lead 5 mg/kg Cadmium 1 mg/kg Mercury 0.1 mg/kg Database of the BAH WG on Contaminants 7100 samples tested on Cd and Pb, 2002-2007 Published* with proposals for limits of 5 mg/kg for Pb and 0.5 mg/kg for Cd with certain exemptions * Gasser U, Klier B, Kühn AV, Steinhoff B. Pharmeuropa Scientific Notes 2009-1 3 Heavy Metals: European Pharmacopoeia Exemptions in individual monographs, e.g. Cd Fumitory 1.5 mg/kg Tormentil 2.0 mg/kg Willow bark 2.0 mg/kg Pb Nettle root (draft) 7.0 mg/kg Iceland moss 10.0 mg/kg 4 2

Heavy Metals: Food and Food Supplements Regulation (EC) No 1881/2006 setting maximum levels for certain contaminants in foodstuffs (in force since 1 March 2007, several amendments), e.g. Pb in vegetables excl. fresh herbs: 0.10 mg/kg Pb in berries and small fruit: 0.20 mg/kg Cd in vegetables excl. fresh herbs: 0.050 mg/kg Cd in fresh herbs: 0.20 mg/kg 5 Heavy Metals: Food and Food Supplements Regulation (EC) No 1881/2006 Pb in food supplements: 3.0 mg/kg Cd in food supplements: 1.0 mg/kg (except seaweed 3.0 mg/kg) 6 3

Heavy Metals: USP Draft monograph no. 2232: Elemental contaminants in dietary supplements Individual component limits for arsenic 1.5 µg/g, cadmium 0.5 µg/g, lead 1.0 µg/g, mercury (total) 1.5 µg/g, methylmercury 0.2 µg/g 10 fold permitted daily exposure (PDE) Three options for compliance: (1) analysis of the serving size compared to PDE, (2) individual component option with daily intake of 10 g, (3) summation option for > 10 g daily intake or individual component limit exceeded 7 Heavy Metals: ICH Development of a Guideline Q3D on Metal Impurities Proposal for class 1 metals ( big four ): arsenic 1.5 ppm, cadmium 0.5 ppm, lead 1 ppm, mercury 1.5. ppm Class 2 metals (moderate safety concerns) and class 3 metals (low safety concern) Herbals are excluded from the scope 8 4

Microorganisms Acceptance Criteria Ph.Eur. Chapter 5.1.4. Microbiological quality of nonsterile pharmaceutical preparations Chapter 5.1.8. Microbiological quality of herbal medicinal products for oral use: Categories A, B, C depending on treatment or pre-treatment which reduces microbial load 9 Microorganisms Acceptance Criteria Ph.Eur. 5.1.8, categories: A. Herbal medicinal products containing herbal drugs, with or without excipients, intended for the preparation of infusions and decoctions using boiling water (for example herbal teas, with or without added flavourings) TAMC (2.6.12) Acceptance criterion: 10 7 CFU/g Maximum acceptable count: 50 000 000 CFU/g TYMC (2.6.12) Acceptance criterion: 10 5 CFU/g Maximum acceptable count: 500 000 CFU/g Escherichia coli (2.6.31) Acceptance criterion: 10 3 CFU/g Salmonella (2.6.31) Absence (25 g) 10 5

Microorganisms B. Herbal medicinal products containing, for example, extracts and/or herbal drugs, with or without excipients, where the method of processing (for example, extraction) or, where appropriate, in the case of herbal drugs, of pretreatment reduces the levels of organisms to below those stated for this category TAMC (2.6.12) Acceptance criterion: 10 4 CFU/g or CFU/mL Maximum acceptable count: 50 000 CFU/g or CFU/mL TYMC (2.6.12) Acceptance criterion: 10 2 CFU/g or CFU/mL Maximum acceptable count: 500 CFU/g or CFU/mL Bile-tolerant gram-negative bacteria (2.6.31) Acceptance criterion: 10 2 CFU/g or CFU/mL Escherichia coli (2.6.31) Absence (1 g or 1 ml) Salmonella (2.6.31) Absence (25 g or 25 ml) 11 Microorganisms C. Herbal medicinal products containing, for example, extracts and/or herbal drugs, with or without excipients, where it can be demonstrated that the method of processing (for example, extraction with low strength ethanol or water that is not boiling or low temperature concentration) or, in the case of herbal drugs, of pre-treatment, would not reduce the level of organisms sufficiently to reach the criteria required under B TAMC (2.6.12) Acceptance criterion: 10 5 CFU/g or CFU/mL Maximum acceptable count: 500 000 CFU/g or CFU/mL TYMC (2.6.12) Acceptance criterion: 10 4 CFU/g or CFU/mL Maximum acceptable count: 50 000 CFU/g or CFU/mL Bile-tolerant gram-negative bacteria (2.6.31) Acceptance criterion: 10 4 CFU/g or CFU/mL Escherichia coli (2.6.31) Absence (1 g or 1 ml) Salmonella (2.6.31) Absence (25 g or 25 ml) 12 6

Microorganisms Method of Determination Ph.Eur. 2.6.12 and 2.6.13: Microbiological examination of non-sterile products 2.6.31: Microbiological examination of herbal medicinal products for oral use: TAMC and TYMC according to 2.6.12 plus tests on specified microorganisms 13 Mycotoxins (Medicinal Products) German Aflatoxin-Verbotsverordnung Not more than 5 µg aflatoxin B 1 per kg and not more than 20 µg aflatoxins B 1, B 2, G 1 and G 2 per kg 14 7

Mycotoxins (Medicinal Products) European Pharmacopoeia Herbal Drugs and Herbal Drugs for Homoeopathic Preparations : where appropriate, limits for aflatoxins/ a limit for ochratoxin A may be required Liquorice dry extract and Liquorice dry extract for flavouring purposes: 80 µg/kg ochratoxin A 15 Mycotoxins (Food) Regulation (EC) No 1881/2006 setting maximum levels for certain contaminants in foodstuffs Aflatoxins in nuts: B 1 2.0-8.0, sum 4.0-15.0 µg/kg Aflatoxins in spices*: B 1 5.0, sum 10.0 µg/kg * Capsicum spp., Piper spp., nutmeg, ginger, turmeric 16 8

Mycotoxins (Food) Regulation (EC) No 1881/2006 Ochratoxin A in dietary foods for special medical purposes intended for children: 0.50 µg/kg Ochratoxin A in spices*: 30 µg/kg from 1 July 2010 and 15 µg/kg from 1 July 2012 Ochratoxin A in liquorice root: 20 µg/kg Ochratoxin A in liquorice extract: 80 µg/kg * Capsicum spp., Piper spp., nutmeg, ginger, turmeric 17 Mycotoxins (USP) USP Chapter 561: Articles of Botanical Origin Not more than 5 µg aflatoxin B 1 per kg and not more than 20 µg aflatoxins B 1, B 2, G 1 and G 2 per kg The extend of testing may be determined using a risk-based approach that considers the likelihood of contamination, and the presence of unexpected contamination is to be considered in determing compliance 18 9

Polycyclic Aromatic Hydrocarbons Regulation 835/2011 amending 1881/2006 Benzo(a)pyrene in oils and fats (excluding cocoa butter) intended for direct human consumption or use as an ingredient in foods: 2.0 µg/kg From 1 September 2012: sum of benzo(a)pyrene, benzo(a)anthracen, chrysene and benzo(b)fluoroanthene:10.0 µg/kg 19 Plant Protection Products: Limits European Pharmacopoeia Chapter 2.8.13 Regulation No 396/2005 on maximum residue levels of pesticides in or on food and feed of plant and animal origin 20 10

Plant Protection Products: Limits European Pharmacopoeia (Ph.Eur.) 2.8.13 List of 70 substances plus metabolites and respective limits Further substances: reference to Regulation 396/2005 oder calculation of limit Validated method to be used Activities of the BAH Working Group on Contaminants: database containing numerous findings from daily practice of the companies 21 Plant Protection Products: Limits Regulation No 396/2005: Website of the European Commission Amendments: http://ec.europa.eu/food/plant/protection/pesticides/co mmunity_legislation_en.htm Database (by products and by substances): http://ec.europa.eu/sanco_pesticides/public/index.cfm 22 11

Plant Protection Products: Limits Annexes to Regulation 396/2005 I: (Groups of) products to which MRLs apply (including herbal teas) II: MRLs formerly defined for products under EC Directives III: Temporary MRLs for defined products IV: Substances for which no MRLs are required (V and VI not yet published, e.g. conversion factors for processed commodities) VII: Fumigants 23 Plant Protection Products: Authorisation Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market (in force since 14 June 2011) Harmonised rules for the approval of active substances and placing on the market of plant protection products including mutual recognition (climatic zones with comparable conditions) Approval of active substances plus authorisation of plant protection products 24 12

Plant Protection Products : Authorisation Regulation (EC) No 1107/2009 The authorisation of a plant protection product may be extended to minor uses (Article 51) Defined as use on plants or plant products which are not widely grown ( Lückenindikationen ) E.g. uses against specific pests/ diseases on medicinal plants 25 Integrated Pest Management Directive 2009/128/EC establishing a framework for Community action to achieve the sustainable use of pesticides Member States shall adopt National Action Plans to set up their quantitative objectives, targets, measures and timetables to reduce risks and impacts of pesticide use on human health and the environment and to encourage the development and introduction of integrated pest management and of alternative approaches or techniques in order to reduce dependency on the use of pesticides. 26 13

Integrated Pest Management keep the use of plant protection products and other forms of intervention to levels that are economically and ecologically justified and reduce or minimise risks to human health and the environment. Member States shall establish appropriate incentives to encourage professional users to implement crop or sector-specific guidelines for integrated pest management on a voluntary basis. Public authorities and/or organisations representing particular professional users may draw up such guidelines 27 Integrated Pest Management Annex III: General principles of integrated pest management Prevention/suppression of harmful organisms, e.g. crop rotation, cultivation, seed and planting material, fertilisation, irrigation, hygiene, beneficial organisms Monitoring by adequate methods Decision on whether to apply plant protection measures Preference of sustainable non-chemical measures Application of pesticides Level/extent of use Risk of resistance Recording and checking success 28 14

Integrated Pest Management Joint project of the German Committee on Medicinal and Spice Plant Cultivation (DFA) and the German Medicines Manufacturers Research Association (FAH): Development of sector-specific guidelines for medicinal and spice plants in accordance with Article 14 and Annex III of CD 2009/128/EC Detailled guidance on how to implement the general criteria to this sector Crop-specific guidance might follow 29 Summary and Conclusion High quality requirements, in particular on contaminants, for herbal medicinal products and related areas guarantee optimum consumer protection Realistic criteria as well as practical experiences should be taken into consideration when new rules are established and when limits are set Preventive measures e.g. reduction of the use of pesticides where justified would minimise the risks to human health and to the environment 30 15