Lawyers Merve Altınay

Merve Altınay

Merve Altınay

Moroğlu Arseven

maltinay@morogluarseven.com

Merve supports clients with intellectual property disputes and litigation, as well as offers day-to-day advice about managing intellectual assets such as trademarks, patents, copyrights and trade dressings. She assists clients to protect, enforce and commercialize these intellectual property rights, as well as assists clients to understand and navigate local regulatory rules. She has particular experience with regulatory compliance in the pharmaceutical, food supplements, advertising, and product liability areas.

She has supported many well-known brands and patents, on both sides of complicated and high-stakes intellectual property disputes. She assists clients to use a range of tools to protect the value and distinctiveness of their assets. These range from coordinating raids and negotiating directly with infringers, through to filing infringement, cancellation or unfair competition lawsuits.


Practice Areas & Work Department

Patents and Utility Models

Trademarks

IP Portfolio Management

IP Litigation

IP Licensing

Anti-Counterfeiting

Domain Names and Internet Infringement

Copyrights

Industrial Designs


Languages

Turkish

English

Düsseldorf UPC Ruling and Turkey: How Far Unified Patent Court Can Extend Its Reach?

On 28 January 2025, Unified Patent Court Düsseldorf Local Division delivered a decision in a patent infringement action brought by Fujifilm Corporation against Kodak GmBH, Kodak Graphic Communications GmBH and Kodak Holding GmBH, which also included a counterclaim for revocation of the patent basis of the infringement claims.

10.02.2025

The Regulation Amending the Regulation on the Licensing of Homeopathic Medicinal Products Has Been Published

The Regulation Amending the Regulation on the Licensing of Homeopathic Medicinal Products was published in the Official Gazette dated December 3, 2024, and numbered 32741, and entered into force on its publication date.

24.12.2024

The Regulation Amending the Regulation on the Licensing of Human Medicinal Products Has Been Published

The Regulation Amending the Regulation on the Licensing of Human Medicinal Products was published in the Official Gazette dated December 3, 2024, and numbered 32741, and entered into force as of its publication date.

24.12.2024

Beşeri Tıbbi Ürünler ve Özel Tıbbi Amaçlı Gıdaların Geri Çekilmesi Hakkında Yönetmelik Yayımlandı

Beşeri Tıbbi Ürünler ve Özel Tıbbi Amaçlı Gıdaların Geri Çekilmesi Hakkında Yönetmelik 23 Ekim 2024 tarihli ve 32701 sayılı Resmî Gazete’de yayımlanmış ve yayım tarihi itibariyle yürürlüğe girmiştir.

25.11.2024

Regulation on the Withdrawal of Medicinal Products for Human Use and Foods for Special Medical Purposes was Published

The Regulation on the Withdrawal of Medicinal Products for Human Use and Foods for Special Medical Purposes was published in the Official Gazette dated October 23, 2024 and numbered 32701 and entered into force as of the date of publication.

21.11.2024

The Medicines and Medical Devices Agency of Turkey Has Re-Evaluated Some of the Health Declaration Statements in the Guideline on the Use of Health Declaration in Food and Food Supplements

In accordance with the Regulation on the Use of Health Declarations in Food and Food Supplements and the Guideline on the Use of Health Declarations in Food and Food Supplements, health declarations may be used in food and food supplements.

05.11.2024

Türkiye İlaç ve Tıbbi Cihaz Kurumu Klinik Araştırmalar Daire Başkanlığına Yapılan Klinik Araştırma Başvurularına İlişkin Kılavuz ile Viral ve Bakteriyel Ajanlara Karşı İnsanlarda Kullanım Amaçlı Hayvan İmmünglobulin/İmmün Serumlarının Klinik Dışı Değerlendirilmesine İlişkin Kılavuz’da Değişiklik Yapıldı

Türkiye İlaç ve Tıbbi Cihaz Kurumu tarafından yayımlanan Türkiye İlaç ve Tıbbi Cihaz Kurumu Klinik Araştırmalar Daire Başkanlığına Yapılan Klinik Araştırma Başvurularına İlişkin Kılavuz’da (“Kılavuz”) İlk Uygunluk Başvurusu, Araştırmalarda Değişiklik Yapılması, Bildirimler, Kurumun Araştırmalarda Gözetimi ve Denetimi ve Diğer Hükümler ayrıntılı olarak düzenlenmiştir.

25.04.2024

Amendments have been Made to the Guideline on Clinical Research Applications to the Clinical Research Department of the Turkish Medicines and Medical Devices Authority, and to the Guideline on Non-Clinical Evaluation of Animal Immunoglobulins/Immune Serums for Human Use Against Viral and Bacterial Agents

The Guideline on Clinical Trial Applications to the Clinical Trials Department of the Turkish Medicines and Medical Devices Agency (“Guideline”), published by the Turkish Medicines and Medical Devices Agency, regulates in detail the Initial Eligibility Application, Amendments to Trials, Notifications, the Agency’s Oversight and Supervision of Trials, and Other Provisions.

22.04.2024
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