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International Conference on Advanced Pharmacy and Clinical Research, will be organized around the theme “Advancing Pharmacy Practice Through Cutting-Edge Research”

PHARMACY CONGRESS 2025 is comprised of keynote and speakers sessions on latest cutting edge research designed to offer comprehensive global discussions that address current issues in PHARMACY CONGRESS 2025

Submit your abstract to any of the mentioned tracks.

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Pharmaceutical biotechnology is a dynamic and rapidly advancing field that utilizes biological systems and organisms to develop new drugs and therapies. This area of biotechnology combines the principles of biology, chemistry, and engineering to address complex medical challenges and create novel treatments.

 

Antimicrobial therapy has been a cornerstone of modern medicine, revolutionizing the treatment of infectious diseases. However, the rise of antimicrobial resistance (AMR) poses a significant threat to global health, necessitating advancements in antimicrobial therapies and strategic efforts to combat resistance. This overview explores the principles of antimicrobial therapy, the mechanisms and impacts of resistance, and the strategies being developed to address these challenges.

 

Pharmacological interventions play a crucial role in the management of mental health disorders, providing relief from symptoms and improving the overall quality of life for individuals. Advances in pharmacology and a better understanding of mental health conditions have led to the development of a diverse range of medications with varying mechanisms of action. Here’s an overview of the key pharmacological interventions for mental health, including their types, mechanisms, benefits, and challenges.

 

Pain management has evolved significantly over recent years, with advances in medical research, technology, and treatment strategies contributing to more effective and personalized care. Innovations in this field aim to enhance pain relief, minimize side effects, and improve patients' quality of life.

 

Pharmaceutical innovations for paediatric and geriatric populations are essential due to the unique physiological, developmental, and health challenges these groups face. Both age groups require tailored approaches to drug development, formulation, and treatment strategies to ensure efficacy, safety, and improved quality of life. This overview explores the key innovations and considerations in paediatric and geriatric pharmacotherapy.

 

Nutraceuticals and herbal medicines represent a diverse category of products derived from natural sources that offer potential health benefits beyond basic nutrition. They have gained popularity for their roles in promoting wellness, preventing disease, and complementing traditional medical treatments. This overview explores the types, benefits, challenges, and considerations related to nutraceuticals and herbal medicines.

 

Case reports of unusual adverse drug reactions (ADRs) provide crucial insights into the safety profile of medications, especially those not fully understood during clinical trials. These reports help identify rare or unexpected side effects that may not be evident in larger, controlled studies and can inform future clinical practice and regulatory decisions.

 

Digital health technologies encompass a broad range of tools and systems that use digital means to improve health and healthcare delivery. These technologies leverage software, hardware, and data analytics to support and enhance various aspects of health management and medical practice.

 

Health economics involves the study of how resources are allocated in the healthcare system, focusing on the cost-effectiveness, efficiency, and value of medical interventions. It provides insights into the economic implications of healthcare decisions and policies.

 

Advanced diagnostics and biomarkers are at the forefront of modern medicine, revolutionizing how diseases are detected, diagnosed, and managed. These innovations are enhancing our ability to provide personalized and effective treatment strategies, improve patient outcomes, and advance our understanding of complex diseases.

 

Pharmacogenomics is the study of how genes affect a person's response to drugs. It combines pharmacology (the science of drugs) and genomics (the study of genes and their functions) to develop personalized medicine strategies. The goal is to tailor drug therapies to individuals based on their genetic makeup, improving efficacy and reducing adverse drug reactions.

Clinical trials for rare diseases, also known as orphan diseases, present unique challenges and opportunities in the field of medical research. Rare diseases are defined as conditions that affect a small percentage of the population, typically fewer than 1 in 2,000 people. Due to their rarity, these diseases often have limited research and treatment options. Clinical trials for rare diseases are crucial for advancing understanding and developing therapies.

 

Pharmacy informatics is a rapidly evolving field that integrates information technology with pharmacy practice to enhance medication management, improve patient outcomes, and optimize healthcare delivery. It encompasses the use of data, technology, and communication systems to support the effective and safe use of medications.

 

Regulatory affairs and drug approval are critical components in the development and commercialization of pharmaceuticals and biologics. This field ensures that new drugs are safe, effective, and of high quality before they reach the market.

 

Advancements in drug formulation are crucial for developing new therapies and improving existing ones. Cutting-edge formulation strategies focus on enhancing drug delivery, increasing efficacy, and minimizing side effects. These strategies leverage modern technologies and scientific insights to address complex challenges in drug development.

 

Pharmaceutical ethics refers to the moral principles and standards that guide the behaviour and decision-making processes of individuals and organizations within the pharmaceutical industry. Pharmaceutical compliance involves adhering to laws, regulations, and internal policies designed to ensure that pharmaceutical companies operate ethically and legally.

 

Biologics are a class of medications derived from living organisms or contain components of living organisms. They are typically large, complex molecules or mixtures of molecules produced through biotechnological methods, such as recombinant DNA technology or cell culture.

Pharmacovigilance and drug safety are pivotal in ensuring the safe use of pharmaceuticals and safeguarding public health. These disciplines focus on the ongoing monitoring and evaluation of drug effects to identify, assess, understand, and prevent adverse effects or other drug-related problems.

Clinical trials are the backbone of medical research and innovation, providing essential data that can lead to ground-breaking treatments and therapies. In recent years, the landscape of clinical trials has seen significant advancements that enhance efficiency, accuracy, and patient engagement.

Advanced drug delivery systems (ADDS) are innovative technologies designed to enhance the efficacy, safety, and patient compliance of therapeutic treatments. These systems focus on improving how drugs are administered, delivered, and released in the body, often by overcoming limitations associated with traditional drug delivery methods.