Lex Analitik invites you to attend our seminar on the legal regulation of pharmaceutical practice and the circulation of medicines, healthcare products and medical equipment in the Republic of Kazakhstan.

Lex Analitik Training Centre would like to invite you to attend our seminar on ‘Legal regulation of pharmaceutical practice and the circulation of medicines, healthcare products and medical equipment in the Republic of Kazakhstan. Bringing the pharmaceutical industry of Kazakhstan into compliance with the GхP (GMP, GDP, GPP) quality guidelines’, to be held on April 25^th - 26^st, 2011 in Almaty.

The purpose of the Seminar is to facilitate and maximise the competitiveness of the businesses working within the rapidly developing pharmaceutical market of Kazakhstan, by keeping them abreast of all developments and pronouncements in the pharmaceutical sector and by providing them with up-to-date information on the statutory and regulatory requirements of the relevant legislation.

According to the State Programme for the Development of Kazakhstan’s Pharmaceutical Industry for 2010-2014, it is the state’s priority primary objective to bring the pharmaceutical industry of the Republic of Kazakhstan into compliance with GхP (GMP, GDP, GPP) quality guidelines. This means that the state aims for all enterprises working within the pharmaceutical market to adopt and comply with the GxP quality guidelines by 2015.

The process of adoption and implementation of the international standards by the local businesses will be examined in detail by Ms. A. Piryanskaya, a consultancy expert in the implementation of international standards (ISO 9001, OHSAS 18001, GxP)

During the Seminar you will learn:

• Good Distribution Practice (GDP) applicable to wholesalers and warehouses;
• Good Pharmacy Practice (GPP), regulating the retail trade of pharmaceutical products;
• Good Manufacturing Practice (GMP) in relation to the modernization of the existing manufacturing processes and the construction of new pharmaceutical manufacturing facilities;
• Legal framework regulating the pharmaceutical sector;
• Licensing of pharmaceutical practice;
• State registration, certification, labeling and advertising of medicines, healthcare products and medical equipment;
• Wholesale and retail trade, handling and storage, termination and export/import within the Customs Union.
• The powers of the competent state authorities overseeing the pharmaceutical sector, upon the inspection of a businesses’ compliance with the law regulating the circulation of medicines in the Republic of Kazakhstan.

The Seminar will be attended by a representative of the competent state authorities, to whom you will have an opportunity to address all your questions and concerns.

We look forward to welcoming: any interested parties, senior managers, lawyers, registration managers, logistics managers, marketing manager, and brand managers of the pharmaceutical companies.

Seminar Speakers:

• Olga Somova, MCIArb, Managing Partner of Lex Analitik Law Firm; Maria Barinova, Associate of Lex Analitik Law Firm. More than 7 years of providing competent legal advice to businesses in the pharmaceutical sector. The speaker’s professional profile can be found at www.lexanalitik.kz
• External Experts: A. Piryanskaya, Consultancy expert in implementation of international standards (ISO 9001, OHSAS 18001, GxP) and a director of Status Training and Consulting non-profit organisation, Krasnodar, the Russian Federation
• Representatives of the competent state authorities

To register as a participant or if you require any further information please contact Ms. Asel Egizbayeva, Administrator for Lex Analitik Training Centre, by calling  8(727)258-48-88, 258-48-89 or emailing a.egizbaeva@lexanalitik.kz

We look forward to welcoming you at the Seminar.