Patenting of an Invention and an Utility Model Whose Object Is an Innovative Medicinal Product by S. V. Vasyliev

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Legal regulation of the economic activities of pharmacies in Ukraine by S. V. Knysh, O. I. Yakymets

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European Union Regulation on clinical trials and Regulation on medical devices: A common soil for future development by Guido Rasi, Alessandro Mugelli

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Regulation 2017/745 on medical devices, two major innovations: 1) the physiological action of devices consisting of natural materials such as vegetal matrices; 2) the chemical-phys... by Marcella Marletta, Marcella Marletta

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Successful transport across continents of GMP-manufactured and cryopreserved culture-expanded human fetal liver-derived mesenchymal stem cells for use in a clinical trial by Ashis Kumar, Sowmya Ramesh, Lilian Walther-Jallow, Annika Goos, Vignesh Kumar, Åsa Ekblad, Vrisha Madhuri, Cecilia Götherström

Subjects: “…Advanced therapy medicinal product…”
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Towards implementing new payment models for the reimbursement of high-cost, curative therapies in Europe: insights from semi-structured interviews by Thomas Desmet, Thomas Desmet, Sissel Michelsen, Sissel Michelsen, Elena Van den Brande, Walter Van Dyck, Steven Simoens, Isabelle Huys

Subjects: “…advanced therapy medicinal product (ATMP)…”
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Trends for Clinical Trials on Medicinal Products for Neurological Disorders in Lithuania and Europe by Emilijus Žilinskas, Arūnas Vaitkevičius

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Role of microglia in the pathogenesis of multiple sclerosis and links to immunomodulatory therapy by P. Valiukevičius, R. Liutkevičienė, R. Balnytė

Subjects: “…advanced therapy medicinal products…”
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Legal Basis of State Support for Creating Innovative Medicinal Products by S. V. Vasyliev

Subjects: “…medicinal products…”
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State Control and State Supervision in the Pharmaceutical Field: Problems of Differentiation by О. S. Khovpun

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Application of four pricing models for orphan medicines: a case study for lumasiran by Noa Rosenberg, Evert Manders, Sibren van den Berg, Lisa J. Deesker, Sander F. Garrelfs, Saco J. de Visser, Jaap W. Groothoff, Carla E. M. Hollak

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Aspects of Regulation of Xenotransplantation in Europe by Ralf Reinhard Tönjes

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DECISIONS OF ROMANIAN LAW COURTS IN CASES CONCERNING THE INTERPRETATION OF ARTICLE 3 (D) OF REGULATION (EC) NO 469/2009 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL OF 6 MAY 2009,... by BUCURA IONESCU

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Development of the institution of criminal liability for abuses on the pharmaceutical market in Russia by D.A. Gusamova

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Medical Devices Made of Substances: A New Challenge by Maria Grazia Leone

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Enlightenment of EU Herbal Medicinal Products regulation on the registration of Traditional Chinese Medicines in the Guangdong-Hong Kong-Macao Greater Bay Area by Ran Xiong, Hui Zhang, Yueyun Li, Guihao Zeng, Yonghui Liu, Yeyou Xu

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PROTECTION OF INVENTIONS IN THE PHARMACEUTICAL SECTOR THROUGH SUPPLEMENTARY PROTECTION CERTIFICATE by Viorel ROŞ

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The role of hospital pharmacists in supporting the appropriate and safe use of CGT/ATMPs: a scoping review of current insights by Junnan Shi, Xianwen Chen, Hao Hu, Carolina Oi Lam Ung

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Multilateral Use of Dandelion in Folk Medicine of Central-Eastern Europe by Robert Gruszecki, Magdalena Walasek-Janusz, Gianluca Caruso, Robert Pokluda, Alessio Vincenzo Tallarita, Nadezhda Golubkina, Agnieszka Sękara

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Unveiling the Potential of C_max <i>f</i>₂ Factor Applied to Pilot Bioavailability/Bioequivalence Studies—A Case Study with Pazopanib Drug Products by Sara Carolina Henriques, Ana Leblanc, Sérgio Simões, Marlene Fonseca, Francisco Luís Pimentel, Luis Almeida, Nuno Elvas Silva

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