RA 8203_ PROHIBITION OF COUNTERFEIT DRUGS.pdf -...

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Unformatted text preview: __ ,,_~M(M»I.ufi-upofl~u~mMW“‘L-»~uo—~u——MV 4_. s - ' I . (Tyegun i S. No. l284 H. N0. 5666 Bepuhlir (If the gliilipyims (Hanging of the filfilippines c{Helm cfllimila fieronb Regular 5255“": [REPUBLIC ACT No. 8203 AN ACT PROHIBITING COUNTERFEIT DRUGS. PROVIDING PENALTIES FOR VIOLATIONS AND APPROPRIATING FUNDS THEREFOR lie it enacted hvl' the Senate and Home uj'chrexenIatives of the -—.— Philippines in (."ongrcxs assembled: SECTION I. Title. - This Act shall be known as the “Special Law r. on Counterfeit Drugs,“ SEC 2. Declaration ofPu/Icv. - It is hereby the policy of the State to protect and promote the right to health of the people and instill health conscrousness among them as provided in Section IS. Article II of the Constitution. and held in Metro Manila. on Monday, the twenty-second dav of July, nineteen hundred and ninety-six. I .I It is also further declared the policy of the State that in order to safeguard the health of the people. the State shall provide for their protection against counterfeit drugs. hi SEC. 3. Definition of Terms. - For purposes of this Act. the terms: a) Drugs shall refer to any chemical compound or biological substance, other than food, intended for use in the treatment, prevention or diagnosis of disease in man or animals, including but not limited to: 1) any article recognized in the official United States Pharmacopoeia-National Formulary (USP-NF), official Homeopathic Pharmacopoeia of the United States, Philippine National Dmg Formulary, British Pharmacopoeia. any National Compendium or any supplement to any of them: 2) any article intended for use in the diagnosis, cure. mitigation, treatment. or prevention of disease in man or animals; 3) any article other than food intended to alTect the structure or any function ofthe body of man or animals: 4) any article intended for use as a component of any articles specified in clauses ( I), (2). (3) not including devices or their components, parts, or accessories; and f5) herbal and/or traditional dnigs which are articles of plant or animal origin used in folk medicine which are: (a) recognized in the Philippine National Dmg Formulary; (b) intended for use in the treatment or cure or mitigation of disease symptoms. injury or bodily defect in man; (c) other than food, intended to affect the structure or any function of the body of man; (d) in finished or ready—to-use dosage form; and (e) intended for use as a component of any of the articles specified in'clauses (a). (b), (c) and (d). b) Counterfeit drug 'merlicine refers to medicinal products with the correct ingredients but not in the amounts as provided hereunder, wrong ingredients. without active ingredients. with insufficient quantity of active ingredient. which results in the reduction of the drug’s safety. efficacy. quality. strength or purity. It is a dnig which is deliberately and fraudulently mislabclcd with respect to identity and/or source or with fake ., t..- enuc ...... , ................. u. .uuv‘rnnb xllvAvVA y. any part of such drug, container or labeling bearing without authorizationthetrademark, trade nameorother identification mark or imprint or any likeness to that which is owned or registered in the Bureau of Patent, Trademark and Technology Transfer (BPTTT) in the name of another natural or juridical person; 2) a drug product refilled in containers by unauthorized persons if the legitimate labels or marks are used; 3) an unregistered imported-drug product. except drugs brought in the country for personal use as confirmed and justified by accompanying medical records: and 4) a drug which contains no amount of, or a different active ingredient, or less than eighty percent (80%) of the active ingredient it purports to possess, as distinguished from an adulterated drug including reduction or loss of efficacy due to expiration. ' c) Brokering shall refer to any act of facilitating the disposal or sale of counterfeit dnigs, including acts of agency. d) Bureau shall refer to the Bureau of Food and Drugs (BFAD) of the Department of Health (DOH). e) Department shall refer to the Department of Health. 0 Business establishment shall referto a'nyentity, whethera single proprietorship, partnership or corporation engaged in, or doing business in the Philippines. g) Owner shall refer to a person or group of persons who is the registered owner of a license to operate a business or business undenaking in the Philippines orthc branch manager oropcrator. licensee. franchisee. or any person acting on behalf of the corporate entity. SEC. 4. l'rohr'bilerl.—'lcls. - 'l'he tel lowing acts are declared unlawful and therefore prohibited: a) The manufacture. sale. offering for sale. donation. distribution trafficking, brokering. exportation, or importation or possession of counterfeit drugs as defined in Section 3 hereof not otherwise covered by Republic Act No. 3720. as amended. The presence or availability of such counterfeit drugs within the premises of any entityengaged inthe sale. manufacture or distribution of drugs and/or pharmaceutical products or in a private residence, or in public or private vehicle, or in the premises not covered by a valid license to operate from the Bureau. shall constitute a primafacie evidence of violation of this Act: Provided, however, That this presumption shall not apply to the legitimate owners of trademarks. trade names or other identifying marks. or the legitimate or authorized representatives or agents of such owners. who have in their possession counterfeit drugs which bear the trademarks. trade names or marksif they can show the sales invoices or official receipts evidencing their purchase from a drugstore. manufacturer or distributor suspected by themofdcaling in counterfeit drugs inyolving the trademarks. trade names and other similar identifying marks registered in their names: Prom-(led. further, That such counterfeit products shall be reported and immediately turned over to the Bureau: Provided, finally. That compliance with the preceding proviso shall be'made within a reasonable period from the date of purchase of such counterfeit drugs as indicated in the sales invoice, official receipt, or other similar documents abovementioned to the time the counterfeit drugs arevreported and turned over to the Bureau; b) Possession of any such counterfeit drugs. However, any person found in possession of counterfeit drugs, in violation of this subsection. shall be excepted from liability under the provisions of this Act after: I) presentation of sales invoices, official receipts, or other legally acceptable documents evidencing his purchase thereof from admgstore. distributor, manufacturer. hospital pharmacy or dispensary. or any other person or place duly licensed to sell and/or dispense drugs or medicines, and indicating therein the batch and lot numbers, as well as the expiry dates of such drugs; or 2) presentation of certificates and other documents evidencing the importation or exportation of the counterfeit drugs found in his possession as required by existing laws, including thoscdocuments required in the preceding paragraph covering the commercial transactions involving counterfeit dnigs. In both cases. the subject counterfeit drugs must not on their face. appear to be as such, or do not bear any marking or any patently unusual characteristic sufficient to arouse the suspicion of a reasonable and prudent person that such dnigs are counterfeit. Furthermore, the amount or volume of counterfeit drugs held is such that it does not negate or is inconsistent with the avermcnt that the same are for personal use. notwithstanding the presentation by the possessor of medical records and other similar documents accompanying andjus1ifying the use of such drugs; c) Forging. counterfeiting. simulating or falsely representing. or without proper authority. using any mark, stamp, tag. label or other identification mark or device authorized or required by Republic Act No. 3720. as amended. and/or the regulations promulgated under this Act; d) Photocopying. duplicating. altering, printing, transferring. obliterating or removing the approved label or any part thereof. lawfully belonging to another person. for the purpose ofusing such label or a part thereof on any counterfeit dnig: Provided. That if the person who committed any of the acts enumerated in this paragraph and the person who used the labels produced thereby are not one and the same person and the former had knowledge of the purpose for which the labels are intended. the former shall also be liable under this Act notwithstanding the failure of the latter to achieve the intended purpose: and c) Making. selling. or concealing any punch. dye. plate or any other equipment or instrument designed to print. imprint or reproduce 6 the trademark. trade name or other identifying n;..rk of another registered producer or any likeness thereof, upon any drug product or device or its container or label without authority from the legitimate owners of the trademark or trade name. SEC. 5. Parties Liable. - The following persons shall be liable for violation(s)-of this Act: . a) the manufacturer, exporter or importer of the counterfeit drugs and their agents: Provided, That the agents shall be liable only upon proof of actual or constmctive knowledge that the drugs are counterfeit; b) the seller, distributor. trafficker, broker or donor and their agents, upon proof of actual or constructive knowledge that the drugs sold. distributed, offered or donated are counterfeit drugs; c) the possessor of counterfeit drugs as provided in Section 4 (b) hereof; ' d) the manager, operator or lessee of the laboratory or laboratory facilities used in the manufacture of counterfeit drugs: e) the owner, proprietor, administrator or manager of the drugstore, hospital pharmacy or dispensary, laboratory or other outlets or premises where the counterfeit dmg is f0und who induces, causes or allows the commission of any act herein prohibited; 0 the registered pharmacist of the outlet where the counterfeit drug is sold or found who, sells or dispenses such drug to a third party and who has actual or constructive knowledge that said drug is counterfeit; and g) should the offense be committed by a juridical person. the president. general manager. the managing partner, chief operating officer or the person who directly induces. causes or knowingly allows the commission ofthe offense shall be penalized. SEC. 6. .4 dministrative Proceedings. - The Bureau is hereby further authorized to undertake the following administrative actions: - M!AF.AmW--.—« - ~——--—-. - mnmlmfimkap-fir'mrl, i l; i l r ( 5 | l r i a) upon ven'fied information on the existence of suspected counterfeit drugs in the possession of any manufacturer, seller or distributor, the duly authorized officers of the Bureau or any officer deputized by the Bureau for the purpose shall segregate, seal and, after having obtained a valid search warrant from a competent court, seize such counterfeit drugs and take them into custody: Provided, That in case the suspected counterfeit drugs are found in a private residence, as defined in Section 3 of this Act or in other premises not covered by a valid license to operate issued by the Bureau, the duly authorized officer of the Bureau or deputized officer thereof shall secure a search warrant for the purpose {\Pf seizing and taking into custody such suspected counterfeit drugs; b) if, afier the appropriate examination of the samples by the, ' Bureau, the seized drugs are determined or found to be counterfeit, the Bureau shall, within fifieen (l5) days from their seizure, issue an order directing the preventive closure of the business establishment for a period not exceeding thirty (30) days. Thereafler, administrative promdings shall be initiated by the Bureau against the parties concerned where they shall have the opponunitytobc heard and presentevidence on theirbehalf; and c) to ensure the effective enforcement of the foregoing, the Bureau may enlist the assistance of the national or local law enforcement agencies. SEC. 7. Administrative Sanctions. - Upon finding that the drugs examined are counterfeit and the determination of the parties liable therefor. the Bureau shall impose any or all of the following sanctions: a) permanent closure of the establishment concerned and the revocation of its license to do business; b) a fine of not less than One hundred thousand pesos (Pl00.000) but not more than Five hundred thousand pesos (P500000); c) upon order ofthe Court. forfeiture. confiscation. and destruction of products found to be counterfeit and the equipment. instruments. and other articles used in violation ofthis Act: d) filing of an appropriate proceedings against the registered pharmacist with the Professional Regulations Commission for cancellation of professional license; e) filing of criminal charges against the violator(s). which can be instituted independently from the administrative case: Provided, That the dismissal of the criminal case shall not lifl the closure order. except when it is a dismissal on the merits or for lack of basis: Provided further, That the withdrawal of the private criminal complaint shall not be a ground for the dismissal ofthc administrative proceedings: and t) permanent disqualification of the person concerned. whether natural orjuridical, from owning or operating an establishment engaged in any business activity under the supem'sion of the Bureau. SEC. 8. Penalties. - The commission of any of the acts prohibited under Sections 4 and 6 ofthis Act shall be punished by: a) imprisonment ofnot less than six (6) months and one ( | ) day. but not more than six (6) years for mere possession of counterfeit drugs as provided for in Section 4 (b) hereof: or b) imprisonment ofsix (6) years and one ( l ) day. but not more than ten (l0) years or a fine of not less than One hundred thousand pesos (Pl00.000) but not more than Five hundred thousand pesos(P500.000) or both such imprisonment and fine at the discretion ofthc coun in any other case mentioned in Section 4 hereof: or c) imprisonment of not less than six (6) months and one (I) day, but not more than two (2) years and four (4) months if the counterfeit drug is intended for animals: or d) imprisonment of not less than six (6) years and one (1) day. but not more than ten (l0) years for any manufacturer. seller or distributor who shall conceal, substitute. dispose or destroy any drug as may have been segregated and sealed by the Bureau. or who shall break. alter or tamperany mark or seal used by the Bureau toidentifythose segregated drugs as provided for urtder SectiOtt 6 (a) of this Act. Any other person . . , w...-...~ .~ In\-1\ol~<‘l‘na‘nv.\u.w~ . . .zvm—u...__. "(M who breaks. alters or tampers any mark or seal used by the Bureau to identify the segregated drugs shall suffer the penalty of not less than six (6) months and one ( l ) day, but not more than six (6) years imprisonment; or e) if. as a result of the use of the drug found to be counterfeit, the illness sought to be cured is aggravated or physical injury or suffering results therefrom, a punishment of imprisonment from twelve (12) years to fifteen (15) years and a fine ranging from One hundred thousand pesos (Pl00,000_) to Five hundred thousand pesos $500,000) shall be meted out; or I) should a counterfeit drug be the proximate cause ofdeath ofa victim, who unknowingly purchased and took a counterfeit drug, the penalty oflife imprisonment and a fine of Five hundred thousand pesos (P500000) to Five million pesos (P5,000.000) shall be imposed;- - In case any act prohibited in Section 4 hereof is also punishable under other laws, the offender shall. if warranted by the evidence, be prosecuted under the law prescribing the highest penalty. SEC. 9. Appropriations. - The amount necessary to cany out the provisions ofthis Act shall be included in the General Appropriations Act for the year following its enactment and every year thereafler. SEC. l0. Implementation. - The Bureau of Food and Drugs of the Department of Health is hereby authorized to administer and supervise the implementation of this Act. SEC. l l. Implementing Rules and Regulations. - Within ninety (90) days from the approval ofthis Act. the Bureau of Food and Drugs. in consultatiOn with the Department of Health. shall promulgate the rules and regulations implementing the provisions of this Act. The implementing rules and regulations issued pursuant to this section shall take effect thirty (30) days after its publication in two (2) national newspapers of general circulation. [0 SEC. l2. Separability ("lause. - If for any reason, any portion or provtsron of this Act is subsequently declared unconstitutional or invalid. such declaration shall not nullify the other portions or provisions hereof. SEC. l3. Repealing Clause. - All laws. decrees, executive or administrative orders, rules or regulations inconsistent with the provisrons of this Act are hereby repealed or modified accordingly. SEC. l4. Efl'ectivity. - This Act shall take effect lifieen (IS) days afler its publication in at least two (2) national newspapers of general circulation. Approved. e, of Representatives 6/ This Act. which is a consolidation of Senate Bill No. [284 and . House Bill No. 5666 was finally passed by the Senate and the House of Representatives on August 27. I996 and August 22, I996. respectively. HE/Z P. GACUTAN Secretary of the Senate W ROBER . NAZARENO Secrel tjv General Ho se 0 Reprexentalives Approved: FIDEL V. RAMOS President of the Philippines 0 CERTIFIED 0 ll / Allnnnit T Amu ...
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