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FORM 20-F Grupo Casa Saba, S.A.B. de C.V.

FORM 20-F Grupo Casa Saba, S.A.B. de C.V.

FORM 20-F Grupo Casa Saba, S.A.B. de C.V.

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Table of Contents<br />

We also offer our customers a series of specialized services, including training, conferences and tra<strong>de</strong> fairs. Some customer services are supported by a monthly<br />

pharmaceutical publication, “Farmservicios Editorial,” formerly “Correo Farmacéutico,” a monthly magazine and product catalog. We have already established an online distribution<br />

and information site for our clients and suppliers, www.farmaservicios.com, which we currently make available to them free of charge. Clients that log on to www.farmaservicios.com<br />

are able to communicate directly with us, and can place and track their or<strong>de</strong>rs and shipments on-line. These clients also have access to a wi<strong>de</strong> range of additional services, including<br />

news and industry information, free e-mail, business advice and a variety of special promotions. www.farmaservicios.com also links to www.farmaservicios.pdv. See “—Information<br />

Technology Systems” above in this item.<br />

Patents and Licenses<br />

Due to the nature of our business, we do not currently have any type of patent. In terms of licenses, we have a sanitary license to operate each of our distribution<br />

centers as well as every one of our pharmacies. In addition, we have licenses that enable us to import products, although they are not material in terms of our sales at this time.<br />

As a result of our broad client and supplier base and the general nature of our business, neither our retail nor distribution business is particularly <strong>de</strong>pen<strong>de</strong>nt on any<br />

type of industrial or commercial contract.<br />

Regulation<br />

In Mexico, both our distribution and pharmacy businesses are primarily regulated by the Ley General <strong>de</strong> Salud, or General Health Law, and the accompanying<br />

regulations. Two fe<strong>de</strong>ral agencies that pertain to the executive branch of the Mexican government, the Mexican Ministry of Health and the Mexican Ministry of Economy, mainly<br />

regulate the pharmaceutical industry. We are required to obtain authorization from the Mexican Ministry of Health to distribute prescription drugs and over-the-counter<br />

pharmaceuticals on the wholesale level. Similarly, the retail sales of pharmaceutical products, health and beauty aids and other merchandise is subject to the General Health Law and its<br />

regulations, state and local health rules and regulations, the Ley Fe<strong>de</strong>ral <strong>de</strong> Proteccíon al Consumidor, or Fe<strong>de</strong>ral Consumer Protection Law, and Normas Oficiales Mexicanas, or<br />

Mexican Official Norms. We are required to obtain a license for each pharmacy to commercialize controlled medicines that contain certain substances. Such medicines cannot be sold<br />

without prescription and sales must be registered in accordance with specific requirements set forth in applicable regulations in control books. We are required to appoint a pharmacist<br />

who must be present at the pharmacy during business hours and who is responsible for compliance with the applicable health regulations in such pharmacy. Such appointment must be<br />

notified to the Mexican Ministry of Health. We believe that we have obtained all necessary authorization and permits required for the operation of our distribution and retail businesses<br />

and we do not foresee any revocation, cancellation or termination of such authorizations and/or permits.<br />

The Ministry of Economy regulates both the wholesale and retail prices of prescription and over-the-counter pharmaceutical products. Mexican law requires us to sell<br />

all prescription and over-the-counter drugs at a price that is equal to or lower than the price approved by the Ministry of Economy for each product. The Ministry of Economy<br />

periodically receives and, if appropriate, approves revised price lists submitted by manufacturers on a product-by-product basis.<br />

The pharmaceutical industry in Brazil operates in highly regulated environment. The pharmaceutical industry is regulated at the fe<strong>de</strong>ral, state and municipal<br />

levels. Fe<strong>de</strong>ral laws and regulations provi<strong>de</strong> a regulatory framework. Enforcement and specific regulation is implemented through state and municipal rules and regulations through<br />

agencies such as the Conselho Regional <strong>de</strong> Farmacia, or Pharmaceutical Regional Council. Pharmacies in Brazil are required to obtain an operating license from the Secretaria <strong>de</strong><br />

Vigilância em Saú<strong>de</strong>, Health Surveillance Secretariat of the Ministry of Health, or SVS, in or<strong>de</strong>r to engage in the handling, distribution, transport, repackaging, import and export of the<br />

substances regulated by the SVS, as well as the medicines that contain such substances. In addition, operating permits, certificates and authorizations must be obtained periodically<br />

from relevant local authorities. All pharmaceutical products and certain non-pharmaceutical products, including certain health and beauty aids, are required to be registered with the<br />

Agência Nacional <strong>de</strong> Vigilância Sanitária, the National Health Surveillance Agency or ANVISA. Although retail pharmacies are not responsible for obtaining registration of the<br />

products sold, pharmacies must check that products offered are duly registered with the appropriate authorities. We believe that we have obtained all the necessary licenses and<br />

permits necessary to operate our business in Brazil.<br />

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