Tractatenblad van het Koninkrijk der Nederlanden
Datum publicatie | Organisatie | Jaargang en nummer | Rubriek | Datum totstandkoming |
---|---|---|---|---|
Ministerie van Buitenlandse Zaken | Tractatenblad 2011, 19 | Verdrag |
Zoals vergunningen, bouwplannen en lokale regelgeving.
Adressen en contactpersonen van overheidsorganisaties.
U bent hier:
Datum publicatie | Organisatie | Jaargang en nummer | Rubriek | Datum totstandkoming |
---|---|---|---|---|
Ministerie van Buitenlandse Zaken | Tractatenblad 2011, 19 | Verdrag |
66 (1989) Nr. 16
Overeenkomst ter bestrijding van doping;
(met Bijlage)
Straatsburg, 16 november 1989
De Engelse en de Franse tekst van de Overeenkomst, met Bijlage, zijn geplaatst in Trb. 1991, 8.
Voor wijzigingen van de tekst van de Bijlage, zie de rubrieken J van Trb. 1995, 114, Trb. 1996, 284, Trb. 1997, 44 en 244, Trb. 1998, 104, Trb. 2001, 98 en 185, Trb. 2003, 40, Trb. 2004, 194 en de rubrieken B van Trb. 2005, 67, Trb. 2006, 33, Trb. 2008, 83, Trb. 2009, 24 en Trb. 2010, 80.
Voor enkele correcties zie Trb. 2008, 83 en Trb. 2009, 24.
De Commissie van Toezicht heeft tijdens haar 32e vergadering op 9 november 2010, op grond van artikel 11, eerste lid, onder b, van de Overeenkomst, te Straatsburg een wijziging van de Bijlage aangenomen. De Engelse tekst van de wijziging luidt als volgt:
Date of entry into force: 1 January 2011
All Prohibited Substances shall be considered as “Specified Substances” except Substances in classes S1, S2.1 to S2.5, S.4.4 and S6.a, and Prohibited Methods M1, M2 and M3.
Any pharmacological substance which is not addressed by any of the subsequent sections of the List and with no current approval by any governmental regulatory health authority for human therapeutic use (i.e. drugs under pre-clinical or clinical development or discontinued) is prohibited at all times.
Anabolic agents are prohibited.
1. Anabolic Androgenic Steroids (AAS)
a) Exogenous1) AAS, including:
1-androstenediol (5α-androst-1-ene-3β,17β-diol); 1-androstenedione (5α-androst-1-ene-3,17-dione); bolandiol (19-norandrostenediol); bolasterone; boldenone; boldione (androsta-1,4-diene-3,17-dione); calusterone; clostebol; danazol (17α-ethynyl-17β-hydroxyandrost-4-eno[2,3-d]isoxazole); dehydrochlormethyl testosterone (4-chloro-17β-hydroxy-17α-methylandrosta-1,4-dien-3-one); desoxymethyltestosterone (17α-methyl-5α-androst-2-en-17β-ol); drostanolone; ethylestrenol (19-nor-17α-pregn-4-en-17-ol); fluoxymesterone; formebolone; furazabol (17β-hydroxy-17α-methyl-5α-androstano[2,3-c]-furazan); gestrinone; 4-hydroxytestosterone (4,17β-dihydroxyandrost-4-en-3-one); mestanolone; mesterolone; metenolone; methandienone (17β-hydroxy-17α-methylandrosta-1,4-dien-3-one); methandriol; methasterone (2α, 17α-dimethyl-5α-androstane-3-one-17β-ol); methyldienolone (17β-hydroxy-17α-methylestra-4,9-dien-3-one); methyl-1-testosterone (17β-hydroxy-17α-methyl-5α-androst-1-en-3-one); methylnortestosterone (17β-hydroxy-17α-methylestr-4-en-3-one); methyltestosterone; metribolone (methyltrienolone, 17β-hydroxy-17α-methylestra-4,9,11-trien-3-one); mibolerone; nandrolone; 19-norandrostenedione (estr-4-ene-3,17-dione); norboletone; norclostebol; norethandrolone; oxabolone; oxandrolone; oxymesterone; oxymetholone; prostanozol (17β-hydroxy-5α-androstano[3,2-c] pyrazole); quinbolone; stanozolol; stenbolone; 1-testosterone (17β-hydroxy-5α-androst-1-en-3-one); tetrahydrogestrinone (18a-homo-pregna-4,9,11-trien-17β-ol-3-one); trenbolone; and other substances with a similar chemical structure or similar biological effect(s).
b) Endogenous2) AAS when administered exogenously:
androstenediol (androst-5-ene-3β,17β-diol); androstenedione (androst-4-ene-3,17-dione); dihydrotestosterone (17β-hydroxy-5α-androstan-3-one) ; prasterone (dehydroepiandrosterone, DHEA); testosterone and the following metabolites and isomers:
5α-androstane-3α,17α-diol; 5α-androstane-3α,17β-diol; 5α-androstane-3β,17α-diol; 5α-androstane-3β,17β-diol; androst-4-ene-3α,17α-diol; androst-4-ene-3α,17β-diol; androst-4-ene-3β,17α-diol; androst-5-ene-3α,17α-diol; androst-5-ene-3α,17β-diol; androst-5-ene-3β,17α-diol; 4-androstenediol (androst-4-ene-3β,17β-diol); 5-androstenedione (androst-5-ene-3,17-dione); epidihydrotestosterone; epitestosterone; 3α-hydroxy-5α-androstan-17-one; 3β-hydroxy-5α-androstan-17-one; 19-norandrosterone; 19-noretiocholanolone.
2. Other Anabolic Agents, including but not limited to:
Clenbuterol, selective androgen receptor modulators (SARMs), tibolone, zeranol, zilpaterol.
The following substances and their releasing factors are prohibited:
1. Erythropoiesis-Stimulating Agents [e.g. erythropoietin (EPO), darbepoietin (dEPO), hypoxiainducible factor (HIF) stabilizers, methoxy polyethylene glycol-epoetin beta (CERA), peginesatide (Hematide)];
2. Chorionic Gonadotrophin (CG) and Luteinizing Hormone (LH) in males;
3. Insulins;
4. Corticotrophins;
5. Growth Hormone (GH), Insulin-like Growth Factor-1 (IGF-1), Fibroblast Growth Factors (FGFs), Hepatocyte Growth Factor (HGF), Mechano Growth Factors (MGFs), Platelet-Derived Growth Factor (PDGF), Vascular-Endothelial Growth Factor (VEGF) as well as any other growth factor affecting muscle, tendon or ligament protein synthesis/degradation, vascularisation, energy utilisation, regenerative capacity or fibre type switching;
and other substances with similar chemical structure or similar biological effect(s).
All beta-2 agonists (including both optical isomers where relevant) are prohibited except salbutamol (maximum 1600 micrograms over 24 hours) and salmeterol when taken by inhalation in accordance with the manufacturers' recommended therapeutic regime.
The presence of salbutamol in urine in excess of 1000 ng/mL is presumed not to be an intended therapeutic use of the substance and will be considered as an Adverse Analytical Finding unless the Athlete proves, through a controlled pharmacokinetic study, that the abnormal result was the consequence of the use of a therapeutic dose (maximum 1600 micrograms over 24 hours) of inhaled salbutamol.
The following classes are prohibited:
1. Aromatase inhibitors including, but not limited to: aminoglutethimide, anastrozole, androsta-1,4,6- triene-3,17-dione (androstatrienedione), 4-androstene-3,6,17 trione (6-oxo), exemestane, formestane, letrozole, testolactone.
2. Selective estrogen receptor modulators (SERMs) including, but not limited to: raloxifene, tamoxifen, toremifene.
3. Other anti-estrogenic substances including, but not limited to: clomiphene, cyclofenil, fulvestrant.
4. Agents modifying myostatin function(s) including, but not limited to: myostatin inhibitors.
Masking agents are prohibited. They include:
Diuretics, desmopressin, plasma expanders (e.g. glycerol; intravenous administration of albumin, dextran, hydroxyethyl starch and mannitol), probenecid and other substances with similar biological effect(s).
Diuretics include:
Acetazolamide, amiloride, bumetanide, canrenone, chlorthalidone, etacrynic acid, furosemide, indapamide, metolazone, spironolactone, thiazides (e.g. bendroflumethiazide, chlorothiazide, hydrochlorothiazide); triamterene, and other substances with a similar chemical structure or similar biological effect(s) (except drosperinone, pamabrom and topical dorzolamide and brinzolamide, which are not prohibited).
The use In- and Out-of Competition, as applicable, of any quantity of a substance subject to threshold limits (i.e. salbutamol, morphine, cathine, ephedrine, methylephedrine and pseudoephedrine) in conjuction with a diuretic or other masking agent requires the deliverance of a specific Therapeutic Use Exemption for that substance in addition to the one granted for the diuretic or other masking agent.
The following are prohibited:
1. Blood doping, including the use of autologous, homologous or heterologous blood or red blood cell products of any origin.
2. Artificially enhancing the uptake, transport or delivery of oxygen, including, but not limited to, perfluorochemicals, efaproxiral (RSR13) and modified haemoglobin products (e.g. haemoglobinbased blood substitutes, microencapsulated haemoglobin products), excluding supplemental oxygen.
The following is prohibited:
1. Tampering, or attempting to tamper, in order to alter the integrity and validity of Samples collected during Doping Control is prohibited. These include but are not limited to catheterisation, urine substitution and/or adulteration (e.g. proteases).
2. Intravenous infusions are prohibited except for those legitimately received in the course of hospital admissions or clinical investigations.
3. Sequential withdrawal, manipulation and reinfusion of whole blood into the circulatory system is prohibited.
The following, with the potential to enhance athletic performance, are prohibited:
1. The transfer of nucleic acids or nucleic acid sequences;
2. The use of normal or genetically modified cells;
3. The use of agents that directly or indirectly affect functions known to influence performance by altering gene expression. For exemple, Peroxisome Proliferator Activated Receptor δ (PPARδ) agonists (e.g. GW 1516) and PPARδ-AMP-activated protein kinase (AMPK) axis agonists (e.g. AICAR) are prohibited.
In addition to the categories S0 to S5 and M1 to M3 defined above, the following categories are prohibited In-Competition:
All stimulants (including both optical isomers where relevant) are prohibited, except imidazole derivatives for topical use and those stimulants included in the 2011 Monitoring Program3).
Stimulants include:
a) Non Specified Stimulants:
Adrafinil; amfepramone; amiphenazole; amphetamine; amphetaminil; benfluorex; benzphetamine; benzylpiperazine; bromantan; clobenzorex; cocaine; cropropamide; crotetamide; dimethylamphetamine; etilamphetamine; famprofazone; fencamine; fenetylline; fenfluramine; fenproporex; furfenorex; mefenorex; mephentermine; mesocarb; methamphetamine(d-); p-methylamphetamine; methylenedioxyamphetamine; methylenedioxymethamphetamine; modafinil; norfenfluramine; phendimetrazine; phenmetrazine; phentermine; 4-phenylpiracetam (carphedon); prenylamine; prolintane.
A stimulant not expressly listed in this section is a Specified Substance.
b) Specified Stimulants (examples):
Adrenaline4); cathine5); ephedrine6); etamivan; etilefrine; fenbutrazate; fencamfamin; heptaminol; isometheptene; levmetamphetamine; meclofenoxate; methylephedrine7); methylhexaneamine (dimethylpentylamine); methylphenidate; nikethamide; norfenefrine; octopamine; oxilofrine; parahydroxyamphetamine; pemoline; pentetrazol; phenpromethamine; propylhexedrine; pseudoephedrine8); selegiline; sibutramine; strychnine; tuaminoheptane; and other substances with a similar chemical structure or similar biological effect(s).
The following are prohibited:
Buprenorphine, dextromoramide, diamorphine (heroin), fentanyl and its derivatives, hydromorphone, methadone, morphine, oxycodone, oxymorphone, pentazocine, pethidine.
Natural (e.g. cannabis, hashish, marijuana) or synthetic delta 9-tetrahydrocannabinol (THC) and cannabimimetics [e.g. “Spice” (containing JWH018, JWH073), HU-210] are prohibited.
All glucocorticosteroids are prohibited when administered by oral, intravenous, intramuscular or rectal routes.
Alcohol (ethanol) is prohibited In-Competition only, in the following sports. Detection will be conducted by analysis of breath and/or blood. The doping violation threshold (haematological values) is 0.10 g/L.
• Aeronautic (FAI)
• Archery (FITA)
• Automobile (FIA)
• Karate (WKF)
• Motorcycling (FIM)
• Ninepin and Tenpin Bowling (FIQ)
• Powerboating (UIM)
Unless otherwise specified, beta-blockers are prohibited In-Competition only, in the following sports.
• Aeronautic (FAI)
• Archery (FITA) (also prohibited Out-of-Competition)
• Automobile (FIA)
• Billiards and Snooker (WCBS)
• Bobsleigh and Skeleton (FIBT)
• Boules (CMSB)
• Bridge (FMB)
• Curling (WCF)
• Darts (WDF)
• Golf (IGF)
• Motorcycling (FIM)
• Modern Pentathlon (UIPM) for disciplines involving shooting
• Ninepin and Tenpin Bowling (FIQ)
• Powerboating (UIM)
• Sailing (ISAF) for match race helms only
• Shooting (ISSF, IPC) (also prohibited Out-of-Competition)
• Skiing/Snowboarding (FIS) in ski jumping, freestyle aerials/halfpipe and snowboard halfpipe/big air
• Wrestling (FILA)
Beta-blockers include, but are not limited to, the following:
Acebutolol, alprenolol, atenolol, betaxolol, bisoprolol, bunolol, carteolol, carvedilol, celiprolol, esmolol, labetalol, levobunolol, metipranolol, metoprolol, nadolol, oxprenolol, pindolol, propranolol, sotalol, timolol.
Zie Trb. 1991, 8.
Zie Trb. 1995, 114.
Zie Trb. 1991, 8 en de rubrieken F en H van Trb. 1995, 114.
Partij |
Onder tekening |
Ratificatie |
Type* |
In werking |
Opzegging |
Buiten werking |
---|---|---|---|---|---|---|
Albanië |
02-02-95 |
15-11-04 |
R |
01-01-05 |
||
Andorra |
29-05-02 |
19-09-06 |
R |
01-11-06 |
||
Armenië |
26-05-00 |
23-03-04 |
R |
01-05-04 |
||
Australië |
05-10-94 |
T |
01-12-94 |
|||
Azerbeidzjan |
28-06-02 |
04-11-03 |
R |
01-01-04 |
||
Belarus |
12-09-02 |
15-03-06 |
R |
01-05-06 |
||
België |
16-11-89 |
30-11-01 |
R |
01-01-02 |
||
Bosnië en Herzegovina |
29-12-94 |
T |
01-02-95 |
|||
Bulgarije |
24-03-92 |
01-06-92 |
R |
01-08-92 |
||
Canada |
06-03-96 |
O |
01-05-96 |
|||
Cyprus |
20-06-91 |
02-02-94 |
R |
01-04-94 |
||
Denemarken |
16-11-89 |
O |
01-03-90 |
|||
Duitsland |
27-05-92 |
28-04-94 |
R |
01-06-94 |
||
Estland |
14-05-93 |
20-11-97 |
R |
01-01-98 |
||
Finland |
16-11-89 |
26-04-90 |
R |
01-06-90 |
||
Frankrijk |
16-11-89 |
21-01-91 |
R |
01-03-91 |
||
Georgië |
02-07-01 |
22-05-03 |
R |
01-07-03 |
||
Griekenland |
10-10-90 |
06-03-96 |
R |
01-05-96 |
||
Hongarije |
29-01-90 |
O |
01-03-90 |
|||
Ierland |
25-06-92 |
29-01-03 |
R |
01-03-03 |
||
IJsland |
25-03-91 |
O |
01-05-91 |
|||
Italië |
16-11-89 |
12-02-96 |
R |
01-04-96 |
||
Joegoslavië (< 25-06-1991) |
10-07-91 |
10-07-91 |
R |
01-09-91 |
||
Kroatië |
27-01-93 |
T |
01-03-93 |
|||
Letland |
23-01-97 |
23-01-97 |
R |
01-03-97 |
||
Liechtenstein |
16-11-89 |
22-05-00 |
R |
01-07-00 |
||
Litouwen |
01-04-93 |
17-05-96 |
R |
01-07-96 |
||
Luxemburg |
16-11-89 |
21-06-96 |
R |
01-08-96 |
||
Macedonië, Voormalige Joegoslavische Republiek |
30-03-94 |
T |
01-05-94 |
|||
Malta |
09-09-94 |
|||||
Moldavië |
20-02-08 |
27-01-09 |
R |
01-03-09 |
||
Monaco |
09-09-03 |
28-11-03 |
R |
01-01-04 |
||
Montenegro |
14-06-06 |
VG |
06-06-06 |
|||
Nederlanden, het Koninkrijk der |
04-12-90 |
|||||
– Nederland: |
||||||
– in Europa |
11-04-95 |
R |
01-06-95 |
|||
– Bonaire |
– |
10-10-10 |
||||
– Sint Eustatius |
– |
10-10-10 |
||||
– Saba |
– |
10-10-10 |
||||
– Aruba |
– |
– |
||||
– Curaçao |
– |
10-10-10 |
||||
– Sint Maarten |
– |
10-10-10 |
||||
Noorwegen |
16-11-89 |
O |
01-03-90 |
|||
Oekraïne |
02-07-98 |
29-11-01 |
R |
01-01-02 |
||
Oostenrijk |
10-05-90 |
10-07-91 |
R |
01-09-91 |
||
Polen |
16-11-89 |
07-09-90 |
R |
01-11-90 |
||
Portugal |
14-06-90 |
17-03-94 |
R |
01-05-94 |
||
Roemenië |
16-06-94 |
07-12-98 |
R |
01-02-99 |
||
Russische Federatie |
12-02-91 |
T |
01-04-91 |
|||
San Marino |
16-11-89 |
31-01-90 |
R |
01-03-90 |
||
Servië |
28-02-01 |
T |
01-04-01 |
|||
Slovenië |
02-07-92 |
T |
01-09-92 |
|||
Slowakije |
06-05-93 |
O |
01-07-93 |
|||
Spanje |
16-11-89 |
20-05-92 |
R |
01-07-92 |
||
Tsjechië |
28-04-95 |
O |
01-06-95 |
|||
Tunesië |
26-02-04 |
T |
01-04-04 |
|||
Turkije |
16-11-89 |
22-11-93 |
R |
01-01-94 |
||
Verenigd Koninkrijk, het |
16-11-89 |
O |
01-03-90 |
|||
Zweden |
16-11-89 |
29-06-90 |
R |
01-08-90 |
||
Zwitserland |
16-11-89 |
05-11-92 |
R |
01-01-93 |
||
* O=Ondertekening zonder voorbehoud of vereiste van ratificatie, R= Bekrachtiging, aanvaarding, goedkeuring of kennisgeving, T=Toetreding, VG=Voortgezette gebonden heid, NB=Niet bekend |
Uitgebreid tot |
In werking |
Buiten werking |
---|---|---|
Bassas da India |
01-03-1991 |
|
Clipperton |
01-03-1991 |
|
Europa-eiland |
01-03-1991 |
|
Frans Guyana |
01-03-1991 |
|
Frans-Polynesië |
01-03-1991 |
|
Franse Zuidelijke en Zuidpoolgebieden |
01-03-1991 |
|
Glorioso-eilanden |
01-03-1991 |
|
Guadeloupe |
01-03-1991 |
|
Juan de Nova-eiland |
01-03-1991 |
|
Martinique |
01-03-1991 |
|
Mayotte |
01-03-1991 |
|
Nieuw Caledonië |
01-03-1991 |
|
Réunion |
01-03-1991 |
|
Sint Pierre en Miquelon |
01-03-1991 |
|
Tromelin |
01-03-1991 |
|
Wallis en Futuna |
01-03-1991 |
Uitgebreid tot |
In werking |
Buiten werking |
---|---|---|
Man |
01-10-1993 |
Denemarken, 16 november 1989
Until further notice the signature of Denmark of this Convention does not engage Greenland and the Faroe Islands.
Griekenland, 7 juli 1994
The Government of the Hellenic Republic declares that the accession of the Former Yugoslav Republic of Macedonia to the Conventions of the Council of Europe to which the Hellenic Republic is a Contracting Party does not imply the recognition of the Former Yugoslav Republic of Macedonia by the Hellenic Republic.
Moldavië, 27 januari 2009
Until the full re-establishment of the territorial integrity of the Republic of Moldova, the provisions of the Convention will be applied only on the territory controlled effectively by the authorities of the Republic of Moldova.
Zie Trb. 1991, 8, Trb. 1995, 114, de rubrieken J van Trb. 1996, 284, Trb. 1997, 244, Trb. 1998, 104, Trb. 2001, 98, Trb. 2001, 185, Trb. 2003, 40 en Trb. 2004, 194, en de rubrieken G van Trb. 2005, 67, Trb. 2006, 33, Trb. 2008, 83, Trb. 2009, 24 en Trb. 2010, 80.
De wijziging van de Bijlage van 9 november 2010 is op 1 januari 2011 in werking getreden.
Wat betreft het Koninkrijk der Nederlanden, geldt de Overeenkomst, die vanaf 1 juni 1995 voor het Europese deel van Nederland gold en vanaf 1 januari 2009 voor de Nederlandse Antillen, vanaf 10 oktober 2010 voor Nederland (het Europese en het Caribische deel), Curaçao en Sint-Maarten.
Zie Trb. 1991, 8, Trb. 1995, 114, Trb. 1996, 284, Trb. 1997, 44, Trb. 2004, 194, Trb. 2006, 33, Trb. 2008, 83, Trb. 2009, 24 en Trb. 2010, 80.
In overeenstemming met artikel 19, tweede lid, van de Rijkswet goedkeuring en bekendmaking verdragen heeft de Minister van Buitenlandse Zaken bepaald dat de wijziging van de Bijlage van 9 november 2010 zal zijn bekendgemaakt in Nederland (het Europese en het Caribische deel), Curaçao en Sint-Maarten op de dag na de datum van uitgifte van dit Tractatenblad.
Uitgegeven de vierde februari 2011.
De Minister van Buitenlandse Zaken,
U. ROSENTHAL
For purposes of this section:
“Exogenous” refers to a substance which is not ordinarily capable of being produced by the body naturally.
“Endogenous” refers to a substance which is capable of being produced by the body naturally.
The following substances included in the 2011 Monitoring Program (bupropion, caffeine, phenylephrine, phenylpropanolamine, pipradol, synephrine) are not considered as Prohibited Substances.
Adrenaline associated with local anaesthetic agents or by local administration (e.g. nasal, ophthalmologic) is not prohibited.
Cathine is prohibited when its concentration in urine is greater than 5 micrograms per milliliter.
Each of ephedrine and methylephedrine is prohibited when its concentration in urine is greater than 10 micrograms per milliliter.
Each of ephedrine and methylephedrine is prohibited when its concentration in urine is greater than 10 micrograms per milliliter.
Pseudoephedrine is prohibited when its concentration in urine is greater than 150 micrograms per milliliter.
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De hier aangeboden pdf-bestanden van het Staatsblad, Staatscourant, Tractatenblad, provinciaal blad, gemeenteblad, waterschapsblad en blad gemeenschappelijke regeling vormen de formele bekendmakingen in de zin van de Bekendmakingswet en de Rijkswet goedkeuring en bekendmaking verdragen voor zover ze na 1 juli 2009 zijn uitgegeven. Voor pdf-publicaties van vóór deze datum geldt dat alleen de in papieren vorm uitgegeven bladen formele status hebben; de hier aangeboden elektronische versies daarvan worden bij wijze van service aangeboden.