Ghazaleh Pouya | Pharmacology | Young Researcher Award

Ms. Ghazaleh Pouya | Pharmacology Science | Young Researcher Award

Ms. Ghazaleh Pouya | Sechenov University | Russia

Ms. Ghazaleh Pouya is an aspiring pharmaceutical scientist and multidisciplinary researcher, currently pursuing a Master’s degree in Biology at Sechenov University with a focus on Innovative Medicines. With a Doctor of Pharmacy (Pharm.D.) degree from the same university, she integrates her clinical pharmaceutical knowledge with advanced research in transdermal drug delivery and AI-powered biomedical solutions. As a lab assistant and assistant researcher, she actively contributes to academic publications, interdisciplinary projects, and data analytics in pharma-biotech. Her curiosity and dedication to translational medicine, wound healing systems, and personalized therapeutics reflect in her dynamic academic and research involvement, positioning her as a promising young innovator at the intersection of pharmacy, biology, and artificial intelligence.

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ORCID

Education

Ms. Ghazaleh earned her Pharm.D. from Sechenov University, completing a thesis on in-vitro modeling of aero-dispersed film-forming systems. Currently, she is enrolled in a Master’s program in Biology, focusing on Innovative Medicines, at the same institution. In parallel, she undertakes applied IT training at School-21, a program dedicated to programming, app development, and clinical data analysis in medicine. Her multidisciplinary training bridges biological sciences, medical informatics, and pharmaceutical technologies. Ms. Ghazaleh’s strong academic background provides her with a unique perspective in drug delivery development and biomedical computation, preparing her for impactful contributions to pharmaceutical innovation and AI-assisted healthcare systems.

Experience

Ms. Ghazaleh Pouya is a laboratory assistant and student researcher at Sechenov University, actively involved in both experimental design and data analysis across pharmaceutical and biological domains, where she develops tools for clinical and pharmaceutical data evaluation. She collaborates with the Department of Pharmaceutical Technology, Department of Biology (Innovative Drugs), and the PHARMA-PREMIUM Scientific Research Center, contributing to a range of wound treatment, drug delivery, and AI-modeling projects. This diverse experience strengthens her competence in translational science, combining wet lab experimentation with computational modeling, ensuring real-world applicability of research findings.

Research Interests

Ms. Ghazaleh’s research focuses on transdermal drug delivery systems, pharmaceutical nanocarriers, and AI-integrated biomedical analytics. She is also exploring in vitro skin models, pharmacogenomics, and quality-by-design (QbD) strategies in formulation development. Her innovative mindset drives her to investigate how machine learning can optimize personalized drug delivery mechanisms, especially for wound treatment and skin permeability. She works on enhancing the bioavailability and targeted release of active substances using nano-based platforms, contributing to the next generation of smart drug delivery systems. Ghazaleh’s vision blends biological sciences, digital health, and pharmaceutical technology for patient-centered therapeutic innovations.

Award

Ms. Ghazaleh Pouya is a strong candidate for the “Young Researcher Award” under the International Invention Awards 2025. Her multidisciplinary background, three completed co-authored publications, ongoing research in pharmaceutical aerosols, and AI-driven drug delivery platforms reflect her impactful contributions at an early stage of her career. Her experience across pharmaceutical formulation, lab analytics, and computational modeling positions her among the emerging leaders in pharm-biotech research. Her self-driven participation in interdepartmental and interdisciplinary collaborations exemplifies the qualities of a future research innovator. This award would not only recognize her current achievements but also catalyze her continued excellence in translational research.

Publications

Transdermal Drug Delivery Systems: Methods for Enhancing Skin Permeability and Their Evaluation

Development of water vapor permeability determination methodology for spray film-forming systems

characterization and screening parameters of spray film-forming systems: a comprehensive study on dosage forms and quality indicators

Conclusion

Ms. Ghazaleh Pouya embodies the ideal profile of a rising biomedical innovator, integrating academic rigor, hands-on laboratory experience, and computational skills into a cohesive research journey. Her contributions to pharmaceutical sciences, particularly in film-forming drug systems and skin permeability, along with her novel integration of AI in drug delivery, showcase her potential to advance therapeutic design. With publications in reputable journals, active institutional collaborations, and an interdisciplinary mindset, she has already laid a strong foundation for a successful career in science and innovation. Recognition through the Young Researcher Award will further encourage her to expand her scientific impact and pursue future breakthroughs in personalized medicine and nanopharmaceuticals.

Dr. Dina Aboushady | Pharmaceutical Analysis | Best Researcher Award

Dr. Dina Aboushady | Pharmaceutical Analysis | Best Researcher Award

German University in Cairo, Egypt.

Dr. Dina Aboushady is a distinguished Postdoctoral Lecturer Assistant in the Faculty of Pharmacy and Biotechnology at the German University in Cairo (GUC), specializing in pharmaceutical chemistry. With a deep passion for drug design and bioanalysis, her research bridges innovative solutions in chiral recognition and pharmaceutical quality. She has significantly contributed to the development of quinazoline derivatives and enantiomeric resolution methods. Her career is marked by numerous awards, including prestigious scholarships and research fellowships. Dr. Aboushady also brings valuable teaching experience to her role at GUC and GIU (German International University).

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Orcid

Education 🎓

Dr. Aboushady obtained her Bachelor's degree in Pharmacy and Biotechnology from the German University in Cairo (GUC) in 2014, graduating with highest honors. She continued her studies and earned a Master's of Science in Pharmaceutical Chemistry in 2016 with excellent grades. Her Doctor of Philosophy (Ph.D.) in Pharmaceutical Chemistry was awarded in 2021, focusing on Quality by Design for Bioanalysis and chiral recognition. Her commitment to research excellence was further recognized with scholarships such as the DAAD/BMBF/GUC funded fellowship and the full Ph.D. fellowship from GUC.

Experience 💼

Dr. Aboushady currently serves as a Postdoctoral Lecturer Assistant at GUC and a Part-time Lecturer at the German International University (GIU), teaching courses like Physical Chemistry, Analytical Chemistry, and Instrumental Analysis. Her teaching extends across several campuses in Cairo and Berlin. Additionally, she has contributed to various workshops such as Grant Writing and LC-MS Essential Operator workshops, emphasizing her active role in academic development and mentoring.

Research Interests 🔬

Pharmaceutical Chemistry Expertise 🔬
Dr. Dina Aboushady specializes in pharmaceutical chemistry, focusing on the design and synthesis of novel drug molecules. Her work includes developing innovative bioanalytical methods that advance the understanding and application of pharmaceutical compounds.

Enantio-Separation and Supercritical Fluid Chromatography (SFC) 🔍
A major part of Dr. Aboushady's research lies in enantio-separation, a process critical to the bioanalysis and quality control of pharmaceutical products. She utilizes supercritical fluid chromatography (SFC), a powerful technique to separate chiral compounds, enabling more precise drug quality assessment and development.

Chiral Recognition in Drug Design 💊
Dr. Aboushady's contributions to chiral recognition are pivotal in optimizing the effectiveness of pharmaceutical products. By understanding and improving how drugs interact with their chiral forms, she plays a crucial role in ensuring that drugs are both safe and effective.

Pharmaceutical Analysis and Drug Quality Control 🔬
Her research in pharmaceutical analysis focuses on improving drug quality control through advanced separation techniques. Dr. Aboushady’s work ensures that pharmaceutical products meet the required standards for efficacy and safety, contributing significantly to drug development and bioanalysis.

Awards 🏆

DAAD/BMBF/GUC Scholarship (2019-2020) for research stay in Germany.

Full Ph.D. Fellowship (2016-2021) at GUC.

Academic Excellence Scholarship (2009-2014) for Bachelor studies at GUC.

DAAD Scholarship for Drug Design Course (Summer 2013) in Germany.

Selected Publications 📚

Aboushady, D., Parr, M. K., Hanafi, R. S., Quality-by-Design Is a Tool for Quality Assurance in the Assessment of Enantioseparation of a Model Active Pharmaceutical Ingredient. Pharmaceuticals, 2020, 13(11), 364.

Aboushady, D., Rasheed, S. S., Herrmann, J., Novel 2,4-disubstituted quinazoline analogs as antibacterial agents with improved cytotoxicity profile. Bioorg Chem., 2021, 117, 105422.

Aboushady, D., Hanafi, R. S., Parr, M. K., Quality by design approach for enantioseparation of terbutaline and its sulfate conjugate metabolite for bioanalytical application using supercritical fluid chromatography. J Chromatogr A., 2022, 1676, 463285.

Aboushady, D., Samir, L., Masoud, A., Chemometric Approaches for Sustainable Pharmaceutical Analysis Using Liquid Chromatography. Chemistry, 2025, 7(1), 11.

 

 

Dr. Natascia Bruni | Chemistry | Best Researcher Award

Dr. Natascia Bruni | Chemistry | Best Researcher Award

Candioli Pharma srl, Italy.

Natascia Bruni is an experienced regulatory compliance and quality management professional with over two decades of experience in the pharmaceutical and feed supplements industries. Currently, she serves as the Compliance Unit Director, Qualified Person, and QPPV at Acel Pharma srl, where she plays a pivotal role in ensuring regulatory compliance, managing product registrations, and overseeing pharmacovigilance activities. Throughout her career, Natascia has worked across various sectors, including pharmaceutical companies (human and veterinary), focusing on quality assurance, regulatory affairs, and strategic business compliance. She is well-versed in navigating complex regulatory landscapes and has made substantial contributions to corporate governance, legal risk management, and quality audits.

Profile

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Orcid

Education 🎓

Natascia Bruni's educational background demonstrates her deep expertise in both scientific and management fields, which has greatly contributed to her successful career in regulatory affairs and quality management. She completed her degree in Chemistry (Nuclear) at the University of Turin from 1991 to 1996, earning the highest distinction with a final vote of 110/110 con lode. This solid foundation in chemistry equipped her with a thorough understanding of chemical processes and analytical methods, which would later be pivotal in her regulatory and quality assurance roles in the pharmaceutical industry.

In addition to her scientific education, Natascia pursued specialized training in Regulatory Affairs and Pharmacovigilance for Drugs between 2001 and 2002, sharpening her skills in the complex regulatory frameworks governing drug safety and compliance. This training became essential in her role as a Qualified Person and QPPV in various pharmaceutical companies, where she led efforts to ensure products met both safety and regulatory standards.

Furthermore, Natascia completed a Business Management Course from 2015 to 2018, which enhanced her leadership, strategic planning, and operational management abilities. This course helped her integrate business and regulatory perspectives, allowing her to lead teams and drive organizational success in compliance-related activities.

Natascia also deepened her technical expertise by attending the School in Technology Enhanced Chemical Synthesis from 1996 to 1999, where she learned advanced techniques in chemical synthesis that continue to inform her work in pharmaceutical and feed supplement regulatory processes. Her multi-disciplinary education has provided a strong foundation for her leadership role in compliance and regulatory affairs, combining scientific rigor with strategic management skills.

Experience 💼

Compliance Unit Director - Qualified Person - QPPV (2012–Present), Acel Pharma srl (Candioli Group), Beinasco (Torino)
Responsible for ensuring the regulatory compliance of raw materials and finished products, overseeing registration/approvals, and managing import/export activities. Works closely with various departments to ensure that all products sold comply with national and international regulations.

Quality Unit Manager & Qualified Person (2007–2012), Olon Spa (Fidia Group), Rodano (MI) and Settimo Torinese (To)
Led the harmonization of QA/QC and regulatory procedures across two sites, ensuring GMP and regulatory compliance for the company’s product portfolio. Managed communications with health authorities and conducted quality audits for suppliers.

Chemistry Department Responsible (1997–1999), Antibiotic Spa, Settimo Torinese (To)
Conducted independent research and developed experimental procedures within the research project scope.

Researcher (1996–1997), Antibiotic Spa, Settimo Torinese (To)
Developed analytical methods and processes in the field of pharmaceutical research.

Research Interests 🔬

Regulatory Compliance in Pharmaceutical Products 📜

Natascia is particularly interested in the regulatory compliance of both raw materials and finished products in the pharmaceutical industry. Her work emphasizes the critical importance of navigating complex regulatory frameworks and ensuring that all pharmaceutical products, especially those used in veterinary medicine, comply with the highest standards of food safety, quality control, and marketing.

Pharmacovigilance & Product Registration 💊

A key area of Natascia's research is in pharmacovigilance, particularly focusing on the monitoring and reporting of adverse effects for drugs, ensuring products maintain safety and compliance throughout their lifecycle. She explores the processes involved in product registration, striving to streamline the approvals and regulatory checks necessary for market entry, particularly in international markets.

Process Improvement Methodologies 🔧

Natascia is also keen on exploring process improvement methodologies within the regulatory compliance space. Her work in this area aims to enhance operational efficiency, reduce legal risks, and strengthen internal control structures. By continuously improving regulatory and operational processes, she contributes to creating a safer and more efficient regulatory environment for pharmaceutical companies, particularly in the feed supplement and veterinary drug sectors.

Awards 🏅

University Senate Award: Best Academic Graduate (1996)
Awarded for excellence in academic performance by the Presidency Council of the Italian Chamber.

OPTIME Award: Best Experimental Dissertation of the Year (1996)
Recognized by the Industrial Union for outstanding research work.

Publications 📚

"Molecular Characterization of the Gorgonzola Cheese Mycobiota and Selection of a Putative Probiotic Saccharomyces cerevisiae var. boulardii for Evaluation as a Veterinary Feed Additive" Published in Applied Microbiology, 2024, 4(2), pp. 650–664.

"Efficacy of a Dietary Supplement in Dogs with Osteoarthritis: A Randomized Placebo-Controlled, Double-Blind Clinical Trial"
Published in PLoS ONE, 2022, 17(2), e0263971.

"Chronic Kidney Disease and Dietary Supplementation: Effects on Inflammation and Oxidative Stress", Published in Veterinary Sciences, 2021, 8(11), 277.
"Chronic Intestinal Disorders in Humans and Pets: Current Management and the Potential of Nutraceutical Antioxidants as Alternatives", Published in Animals, 2022, 12(7), 812.