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admin | Category: Ed Treatment For Migraine | 13.12.2015
Special thanks must also go to our Year 3 and 5 teachers, teacher aides and the Learning Support team, Mrs Melita Haines and Mrs Anne-Marie Schmidt. During the next few weeks we will be practicing our Fire Evacuation and Lockdown Procedures.
As is the case for all emergency procedures, the final process of our Fire Evacuation drill is to debrief with the students.
As we continue to develop powerful partnerships with our families, we felt it was important for you to know of these upcoming arrangements so that you are able to speak with your child, to prepare them or to debrief with them. This week, students in Year 2 to Year 6 will be involved in coding as part of the Junior Campus POP Hour of Code! The Prep and Year 1 students are not missing out as they continue using the BeeBots to develop coding and thinking skills.
To ensure no-one misses out on the fun, all classes on our Junior Campus will get to hear this story during their library lesson next week (Tuesday 24 to Thursday 26 May) and students will also enjoy a variety of fun activities based on the book. To celebrate NSS on Wednesday 25 May, students from Prep to Year 6 are invited to wear a different hat. We look forward to seeing a great variety of hats…funny hats, tall hats, colourful hats, home-made hats – all sorts of hats! To find out more, please join us for our next Open Morning on Tuesday 24 May, where you can participate in a student-led tour and meet key Senior Campus staff.
Reserve your place by booking a tour or contacting Donna Cook, Marketing and Enrolments Manager.
Our Sweet Scandal Special Story is now available in Scandal in the Spotlight for Android!Happy playing! I wanted to try drawing all the characters but got distracted, so here’s grumpy butt actor Rainier Laurent and super rad makeup artist Viola Ferrara. IRELAND Bike Fest, the country’s largest motorcycle festival, returns to Killarney this June Bank Holiday weekend and up to 40,000 people are expected in the town for the event. The event is headquartered at The Gleneagle Hotel with a Bike Village, located on the grounds of The Gleneagle, the main hub of activity.
It is also the ideal spot to sit back and relax after a day’s touring and listen to the live bands and DJ’s perform on the festival’s outdoor stage. Ireland Bike Fest is renowned for its line-up of free live entertainment which takes place across three stages. The Parade through the streets of Killarney will once again take place on the Sunday morning and there will also be the opportunity to win a Harley-Davidson® in the raffle in aid of Muscular Dystrophy Ireland.
Reference pricing in line with the new Draft Resolution of the Cabinet of Ministers and the expected terms of the new model implementation.
The Draft Resolution of the Cabinet of Ministers provoked a lively discussion; in particular it raised a number of practical questions regarding the application of the new procedure of wholesale and retail prices assessment and declaration. Anatoliy Menshikov - taxes and customs, litigationThe Who is Who in Ukrainian Law section is designed to provide a user friendly directory ensuring businessmen and general counsels with a quick snapshot of the legal market landscape structured by firms and individuals. The Law provides for the simplified state registration of medicinal products registered by competent authorities of the USA, Switzerland, Japan, Australia, Canada, and medicinal products registered by competent body of the EU under the centralized procedure. On May 27th, 2016 the Ministry of Health published for public consideration the draft resolution, which provides for the reformation of the declaration system for medicinal products’ wholesale and retail prices. The planned concept involves different approaches to the development of wholesale and retail prices for original medicinal products (in accordance with minimal values in the reference countries) and for generic medicinal products (in accordance with the price for reference original or generic product). Best Lawyers is the oldest and most respected peer-review publication in the legal profession.
It is provided that MOH of Ukraine should establish astandingcommissiononmedicinalproductspricesregulation, which shall decide on the relevance of wholesale-retail prices’ level of declared medicinal product and on the possibility of its inclusion into the register of wholesale-retail prices. Wholesale-retail prices fororiginalforeign medicinal products are proposed to be designated according to the minimal price (and not according to arithmetic average as previously) of one of the reference countries (country of first registration, Bulgaria,  Moldova, Poland, Slovakia, Check Republic, Latvia, Hungary, Serbia). Should be 20% less than the price of reference original product based on minimal level in one of the reference countries. The package of documents required for submission should include the declaration, statement on prices level and power of attorney. When declaring the price for generic product in comparison with the price of other reference generic product it turns out that the price for the first product should be lower than the price for the last one.
From the existing today procedures for wholesale-retail prices declaration there is left the provision left regarding the automatic correcting by the Ministry of Health of the declared prices level, in the case of currency fluctuations. It also should be noted that according to the current CMU Resolution as of July 2, 2014, a„– 240, the wholesale-retail prices for medicinal products purchased under international procurements procedure (centralized procurements) are not subject to mandatory declaration. On amendments to the Regulation on the register of wholesale-retail prices for medicinal products.
Moreover, these or other orders would need to approve the declaration form, statement template for the information on prices level and data sources regarding the level of prices in reference countries. It is also worth to mention that the draft resolution does not provide for the declaration procedure for wholesale-retail prices for medical devices. The Law provides for the simplified registration of medicinal products being registered by the competent authorities of the USA, Switzerland, Japan, Australia, Canada, and the European Union in accordance with the centralized procedure. The registration procedure for such medicinal products envisages the submission of the smaller package of documents, reduction of registration terms (17 business days), and no need for the expertize of the registration materials. The representatives of state authorities (in particular Maksym Nefyodov, Deputy Minister of Economic Development and Trade, and Olexander Starodubtsev, Head of the Department of the Ministry of Economic Development and Trade), real business representatives – pharmaceutical companies, distributors and pharmacy chains, international organizations and professional associations brought together in order to complexly and comprehensively discuss the given issues. Dmytro Aleshko, being a leading expert in the area of state (public) procurements, participated in the profile discussion panel, which opened the conference. The abovementioned Resolution proposes to simplify the state registration procedure for all medicinal products that have already been registered in the USA, Switzerland, Japan, Australia, Canada, and the EU. Novelties in materials expertise for the abovementioned category of medicines and requirements to such materials deserve a special attention. It is worth to mention that despite the fact that the Resolution has not come into effect yet, the text of this legal regulation published on the CMU web-site should be considered as final.
Upon the consideration of the provided materials the Antimonopoly Committee has come to the conclusion that given marketing agreement does not contain any signs of the abuse of monopoly and anticompetitive concerted actions conducted by GlaxoSmithKline Ukraine. Moreover, the project team put major efforts into the materials preparation aimed at the justification of Competition Law non-infringement by the drafted marketing agreement concluded with the pharmacies and pharmacy chains. The document proposes to extend the list of medicinal products liable for simplified state registration, in particular to simplify the procedure for those medicinal products that have already been registered by the competent authorities of the USA, Switzerland, Japan, Australia, Canada or the European Union. The Parliament Health Care Committee did not support this Draft Law and submitted it for further improvement. The Regulation proposes to establish the selection procedures (development of the first draft Essential Medicines List by the Expert Committee) and yearly revision of the National Essential Medicines List. Further, upon the approval of the first Draft National Essential Medicines List the Expert Committee shall revise the existing taking into account the abovementioned factors and sources.
The Draft Regulation also established the schedule of revision of the National Essential Medicines List.
Please note that the Order of the Ministry of Health of Ukraine as of February 11, 2016, a„– 84 approved the Regulation on the National Essential Medicines List and the Regulation on the Expert Committee on the selection and usage of essential medicinal products. For 28 years, The Legal 500 has been analyzing the capabilities of law firms across the world, with a comprehensive research programme revised and updated every year to bring the most up-to-date vision of the global legal market.
The Concept suggests the implementation of activities aimed at solving the issues of timely patients support with qualitative, safe and efficient medicinal products, immunobiological products and medical evices, and activities aimed at the prevention of corruption and limited competition that lead to medicinal products and medical devices procurement at an over-inflated price. The document authors note that the Concept designates the directions, mechanisms and terms for public procurements system transformation in healthcare sector of Ukraine through the development of modern convenient system aimed at the establishment of competitive environment and further development of fair competition in this sector.
The Concept shall be implemented with the assistance of international organizations and donors in three stages during 2016—2018. Stage 1 (2016) – establishment of institutional and legal basis for the reformation of public procurements in healthcare sector. CPO shall fulfill the procurements at local and foreign levels, and if required shall maintain the procurement from international suppliers — import of medicinal products, immunobiological products and medical devices, involve other organizations into customs clearance, storage and distribution, conduct other business activities based on long-term plan principles.
The procedure for insulin products reimbursement foresees that the pharmacy warehouse should file monthly report on the medicinal products sold. Moreover, the document amends the CMU Resolution as of March 5, 2014, a„– 73 "On the Implementation of Pilot Project on State Regulation of Insulin Products Prices" regarding the definition of the unified mechanism of the state regulation of insulin products prices. These medical devices are allowed for market distribution before their expiry date and not later than 5 years from the date of their sales start without the compliance assessment and national quality standard mark. Based on the abovementioned, the compliance assessment procedures shall become obligatory starting from July 1, 2017 for registered medical devices with the unlimited state registration certificate or with the certificate expiring after this date. Another significant change introduces the opportunities to conduct the compliance assessment procedures during the period of validity of medical devices registration certificate.
Moreover, certain changes have been introduced into the registration of the officials responsible for putting medical devices into operation. In case such entity is not a resident of Ukraine, the authorized representative should be assigned with the responsibility to introduce such medical devices into Ukrainian market.
State Administration of Ukraine on Medicinal Products should maintain a Register of entities responsible for the introduction of medical devices into the market. The legal support of the development and adoption of the abovementioned Order of Cabinet of Ministers, as well as the above-mentioned order of the Ministry of Health of Ukraine was provided by the Legal Alliance Company in cooperation with the SIAPS project.
The said provision establishes that the drugs will be included in the National List of Essential Medicines (hereinafter - the National List), taking into account population incidence rates, prevalence of disease and mortality, evidence of the comparative effectiveness (performance), safety and cost-effectiveness of medicines, as well as industry standards  in terms of health and level of funding for health care.
The Expert Committee will consist of 12-18 people, it will be composed of specialists with higher medical, pharmaceutical and economic education.
Once an expert committee under the Ministry of Health of Ukraine is established, work concerning the selection of drugs to be included in the National List will be conducted by them.
Interested individuals and legal entities can apply with a package of necessary documents  for inclusion of drugs in the National List of Medicines. Notice of tax assessment is developed for each separate tax due together with the penalties, as well as for each penalty and poena for the violation of other legislation being under supervision of regulatory authorities.


Notice of tax assessment is considered to be submitted to the taxpayer – legal entity if such assessment notice is delivered by hand to the official employee of such taxpayer against acknowledgement or forwarded in a letter with notification of the delivery. Notice of tax assessment is considered to be submitted to the taxpayer – individual if such assessment notice is delivered by hand to such individual or his authorized representative or forwarded in a letter with notification of the delivery to the address of residence or of the latest known location of such individual. The new Law provides for the implementation of public procurement with the use of two competitive regulatory procedures: open tendering and competitive dialogue, as well as a non-competitive procedure - negotiating the purchase procedure. An important innovation of the Law is the introduction of electronic procurement (e-auction), the electronic review system, as well as the implementation of the exchange of information, documents, to provide clarifications in the e-procurement system. Moreover, for the conduct of unauthorized concentration, which did not lead to monopolization and significant impediment of competition on Ukrainian market , the AMCU recommends to calculate the basic penalty in accordance with the total revenue (income) received from the sales of products (goods, services) at all commodity markets of Ukraine. The AMCU made the greatest specification regarding the calculation of the basic penalties in the cases of the infringements of informational character.
Moreover, the AMCU believes that if the incorrect information has been provided several times during the consideration of the case regarding the violation of informational character, the total penalty charges shall amount to the penalty for one relevant violation.
It is worth to mention that the AMCU established the reduced penalty, which may be imposed on the respondent during the investigation of the case of informational character and on the applicant in the case regarding the concentration and the concurrent actions if they provided incomplete case information.
Correction of previously determined penalty taking into consideration the aggravating and mitigating circumstances.
Declarations with violation of the deadlines for submission for the reporting period in case the application is submitted within its contents. The registers are published at the official State Fiscal Service’s web-site on a daily basis.
In case the Main Directorates of the State Fiscal Service in regions, or in the city of Kyiv send to the appellant the decision on final or partial denial of the appeal, the appellant has a right to file the subsequent appeal within 10 calendar days upon the receipt of such decision. The document in its new edition, updated and improved in line with the requirements of the Law of Ukraine "On Prevention of Corruption", was recently approved by the  Management Board of AIPM Ukraine. The project was conducted by Oleksii Bezhevets, partner with Legal Alliance Company and senior associate Lidiya Sangarovskaya-Gurlach. The most important among the suggested amendments is the one concerning the Procedure of monitoring of adverse reactions to medicinal products permitted for medical use as approved by decree a„– 898 of the Ministry of Health of Ukraine, dating December 27, 2006 (hereinafter - the current procedure), in the new edition, changing its name to "The Procedure for the Conduct of Pharmacovigilance" (hereinafter - the new procedure).
Thus, the new procedure determines that the applicant may have more than one system of pharmacovigilance, for example, specific systems for different types of medicines (vaccines, OTC drugs, etc.). With regards to the authorized person, the new order establishes that in the case of the applicant, who is located in Ukraine, the authorized person must be part of the applicant's personnel.
The new procedure defines the document with a detailed description of the pharmacovigilance system as a Pharmacovigilance System Master File (PSMF).
An important achievement of the new procedure is to establish the requirements for the system of risk management in pharmacovigilance.
In contrast to the existing rules, the new procedure provides for the obligation of creating a risk management plan.
In concern with medicinal products that do not require the creation of risk management plans, the applicant must support the specification file of important identified risks and important potential risks with the aim of preparing regular reports. In terms of other amendments foreseen by the new procedure, emphasis should be given to the advanced categorical apparatus and a new player in the field of pharmacovigilance - rapid response groups of relevant departments of Health, which are responsible for investigating all serious adverse events after immunization and some others. Therefore, the adoption of the new order will contribute to the harmonization of national legislation with the European legislation.in the field of pharmacovigilance. It is to be recalled that  in their time some of the provisions were "the bone of contention" between the regulator and the subjects of the pharmaceutical market.
Therefore a situation may arise where the abovementioned provisions will be in force before the relevant decision of the Cabinet of Ministers' of Ukraine albeit with the edition of order a„– 143.
The abovementioned draft legislation proposes the disclosure of information contained in the materials of the pre clinical studies and the clinical trials that are attached to the application for the registration of the medicinal product. In the opinion of the legislation draft's initiators, the closed nature of such data results in the circulation of drugs, whose effectiveness and safety have not been proved. The Project aims to supporting of Ukrainian government in issue of improvement of effectiveness and transparence in public purchasing system for medicinal products, in particular, by complying of National list of main medicinal products and medical devices with international standards. This year the event attended 130 representatives of the pharmaceutical sector, specialized media, non-governmental organizations, professional associations, and state regulatory authorities.
In the beginning of the session Dmytro Aleshko presented a report on the regulation of the medicinal products and medical devices market. Taking into consideration the composition of the event members many of whom represented the medical devices market, the regulation of the medical devices circulation in 2016 was discussed during a separate interactive session involving Pavel Harchyk, President of the Association of market operators of medical devices, Natalia Serhienko, Health Care Committee Executive Director, European Business Association, and Darya Bondarenko, CEO of Association of market operators of medical devices. The next session of the conference touched the most current issues of the organization of corporative ethics and anticorruption compliance system in the pharmaceutical business. Following the traditions of the summery conferences the session on taxation of pharmbusiness was held.
The highly topical conference programme did not let the participants to relax and loose focus, just as the regulatory and law-enforcement authorities does not let the sector representatives to relax in the course of the year. Our students should be extremely proud of the way they approached the week, each test individually and the anxiety that can sometimes accompany such assessments. Each of these staff members has provided much-needed support for our students during and prior to the NAPLAN week. This is important to help them understand that it was only a practice, to make sure everyone is feeling okay and to remind our students of how they went and areas they might need to improve in. The recent events at a fellow Lutheran school, St Andrews Lutheran College, have reminded all how important safety is and that when well prepared and rehearsed a much better outcome can be achieved. It was a new skill for many teachers and an excellent opportunity for collaborative problem solving. Additionally, it is part of the Australian Technologies Curriculum and if the teachers are any guide, it will be engaging and a lot of fun! This book will be read aloud to children in schools, hospitals, libraries and homes as part of National Simultaneous Storytime (NSS).
Everyone here at Trainwreck is a big fan of Dustin’s and we’re excited to announce his participation in the game! Here visitors can browse the many trader stands selling all kinds of specialised biker wares or dine at one of the festival’s many food outlets. This year’s packed programme includes performances by The Unusual Suspects, J90, R&B, Blue Moose, Hell Raiser, Newfoundland, Hells Bells, Crossroads66, The Small Hours, Sin Iad, Live Lizzy and Devious.
Taking into consideration the expected terms of enactment of the new reference pricing model, we deem this workshop as quite important and useful. A Handbook for Foreign Clients — a guide that annually does a solid research of the Ukrainian legal market, analyses trends and forecasts of market development. The Law on Simplified Registration of Medicinal Products Registered in the Countries with Strict Regulatory Policy.
These medicinal products should be allowed for use on the territories of the abovementioned countries or the EU member-states.
Kostincommented on the review outcomes «In legal areas we practice it is very important to remain faithful to ourselves and our authority. A listing in Best Lawyers is widely regarded by both clients and legal professionals as a significant honor, conferred on a lawyer by his or her peers. Commission shall be composed of the representatives of Ministry of Economic Development, Ministry of Social Policy and Ministry of Finance of Ukraine. It is worth to mention that currently this provision cannot be implemented, as the procedure of such correcting is not established.
At the same time, in the newly developed by the Ministry of Health draft procedure such exception is absent. Gorbatenko shared the structure of the smart office and the insights of the associates working remotely.
Remote work has significantly changed the style of life and work of our lawyers, it has moved the Company closely to our Clients and partners in other jurisdictions”. Such products should be accepted for usage in the territories of the mentioned countries or the EU member-states.
Thus, the term for materials expertise conducted by the State Expert Center has been reduced to 20 business days.
The Resolution proposes the Ministry of Health to establish the expertise procedures for the abovementioned products, but with an approval of the Ministry of Economic Development.
This Draft Law also proposes to establish the simplified registration procedures for all medicinal products that have already been registered in the USA, Switzerland, Japan, Australia, Canada, and the EU.
In particular, the team made a comprehensive research on medicinal product markets, which may be affected by the concluded marketing agreement, conducted social and marketing studies, analyzed the experience of GlaxoSmithKline group of companies regarding the relevant agreements in other countries, developed internal standard operating procedures for the Client with regard to pharmacies and pharmacy chains cooperation.
We would also like to express our gratitude to the project team members representing GlaxoSmithKline Ukraine for the fruitful collaboration.
The Draft Law was initiated by the Cabinet of Ministers of Ukraine and presented the same say at the Government session.
This Regulation belongs to the package of documents drafted in order to implement the new model of Essential Medicines List. The difference lies in the fact that all individuals intending to include a particular medicinal product into the List shall have an opportunity to submit a corresponding application including the documents confirming the comparative efficiency, safety and cost-effectiveness of the product.
The Regulation Annexes formalize the application execution Instruction for amending the National Essential Medicines List. The adoption of the Draft Resolution shall promote the establishment of professional centralized procurement organizations (hereinafter - CPO) in Ukraine, which requires some time and incremental actions. CPOs shall be established under the Health Ministry decision and shall operate under its supervision.
During this period all medical devices shall be introduces to the market and put into operation on the basis of acting certificate of state registration. Registered medical devices with the certificate expiring after July 1, 2017, should undergo the compliance assessment procedures after the expiration of such certificate in order to stay on the market. The structure and contents of national lists will be based on the latest edition of the Basic List of Essential Medicines recommended by WHO.


An important step forward is the need to study whether or not such persons present a conflict of interest, as well as the possibility of participation of foreign specialists with the necessary knowledge and experience in the selection process in the national list,"- said Dmytro Aleshko, who heads the team of experts developing a normative - regulatory package  on this matter.
Such persons shall not present a real conflict of interest, in particular,  they should not be in an employment or any other contractual relationships with producers and holders of certificates of registration of drugs or associated persons. At the same time, the Law provides a number of cases to which the provisions of the latter do not apply. In addition, the AMCU has specified the meaning of such aggravating circumstances as the obstruction of case investigation.
This method is recommended in case the respondent did not provide any information on the total revenue at the market where the concentration took place and at adjacent markets. Thus, previously the basic penalty equaled up to 5% of the revenue from the sales of the products (goods, works, services) of economic entity in the last reporting year prior to the year the penalty was charged, and if there was no revenue or the respondent did not provide any information on the total revenue – the penalty equaled to 10 000 of non-taxable incomes of the residents. The written appeal should contain all data outlined in the Procedure, it should be signed by the appellant-physical entity or by the authorized person, for other appellants – the appeal should be signed by the director or a legally authorized representative and sealed (if available). Thus, the new procedure provides a number of new features, the most interesting of which relate to the applicant. At the same time, each applicant's pharmacovigilance system can have only one authorized person responsible for the pharmacovigilance (hereinafter – authorized person). Should the applicant not be located in Ukraine, then a contact person for pharmacovigilance in Ukraine, who is a subordinate of the applicant's authorized person, must be assigned on the territory of Ukraine.
In comparison with the current procedure, the new procedure establishes simultaneously a clear framework for such PSMFs with the requirements for information that must be contained in it. It should be noted that the current procedure contains a provision, according to which the applicant creates a pharmacovigilance risk management plan, i.e.
The draft resolution prepared by the Ministry of Health of Ukraine , does not contain any significant differences , except for some editorial amendments. The matter concerns a three-way contract, the requirement for the conclusion of which seems by importers to not be feasible.
Therefore the draft legislation at hand is aimed at initiating access to such information, which will enable all interested citizens, their associations and professionals to decide on the selection  for the appointment and the medical use of the medicinal products on the basis of objective data concerning the level of proof on their safety and effectiveness. Being an annual event for the pharmaceutical sector representatives, the Conference focuses on the regulatory aspects of the pharmbusiness and other legal tendencies of the pharmaceutical market. Krzysztof Siedlecki, European Business Association President, Astellas Pharma Europe BV Country Manager Ukraine, Dr. The discussion was held around the current status, potential problems and roadmaps in this sphere. The session was opened by Legal Alliance Partner Oleksii Bezhevets, who informed the participants on the main changes in anticorruption requirements. Legal Alliance Associate Partner Andrii Gorbatenko, who leads the antimonopoly and competition law practice, acted as a moderator of this session.
Nevertheless, all the attendees remained satisfied with a quantity and quality of the information received at the event and expressed a desire to meet in such a format at least twice a year. At the end of last week, each year level had a small celebration to acknowledge their achievements. The Year 2 students performed extremely well in their last Junior Cross Country, tackling the hill sections with gusto. During this time, the students will be walking through the entire Fire Evacuation process so that they know what to do and where to go in the event of an actual fire evacuation. If you have any concerns or would like further information, please contact your child’s teacher. At the centre of these skills is a belief that people will need to use analytical skills to organise, clarify, process, then imagine and create the possibilities, connecting ideas considering all alternatives. Don’t forget to ask your child about their coding, and maybe spend a little time together honing those analytical skills. Curious ladies and dudes will have to contact the irl-source for current romantic eligibility. On the one hand, the market participants expressed the problems they may face when assessing and declaring the prices under the new procedure. It is designed to give the readers an exhaustive and precise picture of market over the past years, including law firms’ performance according to the legal practices and markets they are involved. Therefor, the CMU actions plan for the period by September 30th, 2016 it is scheduled to implement the new principles of pricing aimed at reducing the budget expenses at tenders up to 30%. His report, in particular, revealed the instruments and technologies being used in Legal Alliance for the organization of such work. They gave the participants the opportunity to make the most objective opinion on the changes in the field of public procurements. During another session he presented a report on “Law Labyrinth of Legal Support and Appeal of Procurements Outcomes.
The term for making the decision on or the rejection of the state registration has been reduced to 10 business days.
Please note, that the Ministry of Economic Development is mentioned for the first time in the context of the state registration of medicinal products and previously was not involved into any step of the registration process. In addition, we would like to mention a substantial expertise and due attention to this issue expressed by Antimonopoly Committee specialists. The reimbursement of insulin products costs shall be fulfilled at the rate of reference price for the medicinal product approved by the Ministry of Health of Ukraine. The patients shall receive their medication for a lowered price or for free in accordance with these categories. Business entity should submit the relevant report not later than the 5th day of the month following the reporting month, and in December — not later than the 24th day of the reporting month. An important selection criterion is the presence of experience of the evaluation of the comparative efficacy (effectiveness), safety and cost-effectiveness of drugs.
This Order updates the mailing procedures for tax assessment notices to be sent to taxpayers by regulatory authorities.
Today the AMCU increased the penalty up to 30% of the revenue from the sales of the products (goods, works, services) that violated the legislation on the protection against unfair competition. In the end of the session the Legal Alliance senior associate Alexander Bondar presented a report on the new public procurements law, which practically implements the electronic procurements (electronic auction), electronic system of appeal, and the exchange of information, documents, submission of explanations in the electronic procurements system. In the course of his report the delegated had an opportunity to discuss the plans and implementations of 2015 and to share their expectations and forecasts for the coming year.
After he passed the floor to the special guests of the conference - Aliona Kushnova, Judge at the regional Kiev administrative court, and Jonas Triggvason, Managing Partner, UPharma Consulting. The session was traditionally opened with an analytical report on the status of the pharmaceutical market in 2015 presented by Irina Gorlova, General Director, SMD. Vitalii Savchuk, Senior Associate, Legal Alliance, presented a report on the most high-profile cases, investigations and court practices regarding the pharmaceutical industry. Thanks must also be extended to our families for their support in ensuring they were well rested and well fed for the assessment.
Our Year 1 students settled into their longer run, including a stretch up ‘heartbreak hill’ while our Preppies were as ever, extremely cute. This was an opportunity for the students to listen to our Fire Evacuation and Lockdown sirens.
This is a joint work of all Legal Alliance Team and a perfect motivation for further achievements». Our joint efforts led us to the implementation of the project that only yesterday seemed to be almost impossible”.
The reports should be submitted to local budgets holders who have been legitimately assigned for the execution of operating expenses of local budgets for preferential provision of insulin products to diabetic patients defined by the decisions on such expenditures in accordance with the legislation for the reimbursement to business entity of the amount stated in the register within 15 days upon the report receipt. In addition to a lot of interesting facts the reporter highlighted that the total volume of the medicinal products market in Ukraine amounted to 2.1 billion USD in 2015. Their enthusiasm never fails to move those who are fortunate enough to watch the Preppies participate. During this time the classes did not have to respond to the bells, but were able to have a conversation with their classroom teachers about how to distinguish between the two sounds.
The topic discussed was “The Law on Simplified Registration of Medicinal Products Registered in the Countries with Strict Regulatory Policy. Volodymyr Redko, Executive Director of Association of Pharmaceutical Research and Development APRaD. Sincere thanks must go to our Year 6 classes and their teachers as the support teams for each year level, Mrs Molkentin on first aid and of course Mr Wooding, who organised another very successful and highly enjoyable carnival event. This will provide us with an opportunity to rehearse our processes under a more spontaneous situation.
In the framework of this session the participants discussed the adjustments in the personal data protection, as well as promotional activities and programs of the pharmaceutical companies. Special thanks must also go to our Auxiliary for providing tea, coffee and sweet treats for the visitors.
The best retail figures are shown by dietary supplements, patients care items and medicinal products, the worst figures – personal care products and cosmetics. Session speakers - Zoya Zamikhovska, Junior associate, Lidiya Sangarovskaya-Gulach, Senior associate, and Andrii Gorbatenko, Associate partner, who presented to the audience their reports on medicinal products advertising, marketing agreements in the pharmacy sector, and distribution contracts. Andrii Gorbatenko emphasized the types of law infringements foreseen by the competition law, and paid the attendees attention to the provisions of distribution contracts, which are attracting a close attention of the Antimonopoly Committee of Ukraine, in particular the provisions regulating the reports, discounts and bonus payments.



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