32^nd Annual European Pharma Congress April 25-26, 2022 Barcelona, Spain

Medical devices are rapidly advancing from traditional hardware-based systems to include, or be, biological materials. In many cases these biomaterials are derived from an individuals's own cells. To recognize the convergence of bio-engineering and medical devices the term biomedical device is used. Regenerative medicine, CAR-T, and gene therapy are three significant areas of biomedical device research and development. As the industry grows, so do the jobs and demand for technical personnel to support the manufacturing processes.

Biologic drugs are large, complex proteins made from living cells through highly complex manufacturing processes. Unlike generic drugs, which are copies of chemical drugs, a biosimilar is a copy of a biologic medicine that is similar, but not identical, to the original medicine.
 

Pharmaceutical research and development (R&D) is funded from a complex mix of private and public sources. Governments mainly support basic and early-stage research through direct budget allocations, research grants, publicly owned research institutions and higher education institutions.

Advantages of advanced drug delivery systems over traditional systems are the ability to deliver a drug more selectively to a specific site; easier, more accurate, less frequent dosing; decreased variability in systemic drug concentrations; absorption that is more consistent with the site and mechanism of action.

Drug discovery is the process through which potential new medicines are identified. It involves a wide range of scientific disciplines, including biology, chemistry and pharmacology.

Coronaviruses (CoVs) are distributed worldwide and have various susceptible hosts; CoVs infecting humans are called human coronaviruses (HCoVs). Although HCoV-specific drugs are still lacking, many potent targets for drug discovery are being explored, and many vigorously designed clinical trials are being carried out in an orderly manner. During the spread of COVID-19 outbreak, great efforts have been made in therapeutic drug discovery against the virus, although the pharmacological effects and adverse reactions of some drugs under study are still unclear. However, well-designed high-quality studies are needed to further study the effectiveness and safety of these potential drugs so as to provide valid recommendations for better control of the COVID-19 pandemic. 

Pharmaceutical digital marketing, however, offers immense opportunity for your organization to promote its brand and products to the right audience, from doctors to patients. You can use multiple channels and techniques to build a competitive and legal pharma marketing strategy. Drug marketing is the management process that serves to identify and meet patients. Generally company uses many techniques for the product promotion it mainly includes sales promotion and business marketing. It’s a crucial element in pharmaceutical innovation. Social media is often more used to get attention online.

• Future of Pharma and R&D
• Entrepreneur Investment Meet
• Journal articles and technical documentation
• Marketing Strategies
• Market Analysis

With the COVID-19 pandemic, we are living through a world crisis the likes of which hasn’t been seen in 100 years. The COVID-19 situation is particularly stressful because it’s hard to predict how things will develop, and our circumstances are changing rapidly. This can leave us feeling powerless, like we’re no longer in control of our own lives. As is the case in many aspects of our lives, there are things we can’t control in this situation. These include the actions and reactions of other people, how long the situation will last, and what might happen in the future.

Epidemic outbreak of Covid19

Infection Control

Treatment & Cure

Risks Factors & Prevention

Diagnosis & Detection

Quality assurance is a way of preventing mistakes and defects in manufactured products and avoiding problems when delivering products or services to customers; which ISO 9000 defines as "part of quality management focused on providing confidence that quality requirements will be fulfilled.

Clinical pharmacy is a health science discipline in which pharmacists provide patient care that optimizes medication therapy and promotes health, and disease prevention. ... Hospital pharmacy is a specialization of this field that includes additional duties such as aiding doctors in applying drug therapy.

Genomics and proteomics are closely-related fields. The main difference between genomics and proteomics is that genomics is the study of the entire set of genes in the genome of a cell whereas proteomics is the study of the entire set of proteins produced by the cell

Small molecules have long been the basis for drug development. ... Large molecules, or biologics, are classified as proteins having a therapeutic effect. In contrast to small molecule drugs, most large molecule drugs are complex and composed of more than 1,300 amino acids and are identical versions of human proteins

Physiologically based pharmacokinetic (PBPK) modeling is a mathematical modeling technique for predicting the absorption, distribution, metabolism and excretion (ADME) of synthetic or natural chemical substances in humans and other animal species.

An in vitro in vivo correlation (IVIVC) is a predictive mathematical model that describes the relationship between an in vitro property of a dosage form and a relevant in vivo response. ... IVIVC is important for many different scenarios but is especially important for extended release oral formulations.

Regulatory Affairs contributes essentially to the overall success of drug development, both at early pre-marketing stages and at all times post-marketing. The pharmaceutical industry deals with an increasing number of interesting drug candidates, all of which necessitate the involvement of the quality assurance in regulatory affairs department.

Drug safety is otherwise called Medication Safety in the field of health. It is related with antagonistic impacts of Pharmaceutical items including numerous other logical perspectives, for example, the reactions of medications, the nature of solutions, prescription mistake in utilization of medications, absence of viability of medications, and fake medications. Tolerant Safety, Drug Interaction (drug–drug and food–drug cooperation) Drug Pharmacokinetic, and Adverse Drug Reaction are a few terms required with Drug Safety.

Pharmacovigilance is the science and exercises identifying with the discovery, evaluation, comprehension and counteractive action of unfavorable impacts or some other pharmaceutical related issue. Pharmacovigilance underpins general wellbeing programs by giving solid data to the productive evaluation of the hazard advantage profile of solutions, add to the appraisal of formal, uses, symptoms, damage, viability and danger of pharmaceuticals, empowering the sheltered, sound and more viable utilization of different medications. Advance instruction, understanding and clinical preparing in Pharmacovigilance and its successful accessibility to people in general.

Pharmaceutical nanotechnology has a new scope of study with better opportunities in different areas of diagnosis and treatment. ... It is well-established as a specialized area for drug delivery, diagnostics, prognostic and treatment of diseases through its nano engineered tools. Nanotechnology is now widely regarded as the enabling technology of the 21st century. Today nanostructured materials and nanotechnology techniques are being used to produce better composite materials, materials with  enhanced catalytic activity, hardness and scratch resistance,  and a wide range of  consumer  products (such as cosmetics and sunscreens) that improve human life.

Drug regulation is the control of drug use by international agreement and/or by regulatory authorities such as the US Food and Drug Administration (FDA), the European Medicines Agency (EMA) and the Japanese Pharmaceutical and Medical Devices Agency (PMDA).

Pharmacology is the branch of biology concerned with the study of drug or medication action, where a drug can be broadly defined as any man-made, natural, or endogenous molecule which exerts a biochemical or physiological effect on the cell, tissue, organ, or organism.The  drug market was valued at nearly $5.8 billion during  2011 and will reach nearly $5.7 billion during   2012.  Total value is expected to reach nearly $5.4 billion in  2017.

Pharmacognosy, a long settled pharmaceutical science, has assumed a various part in the disclosure, characterization, generation and institutionalization of these medications. The importance of this train regarding examination and instructing has expanded in the most recent decade as individuals from the general population in created nations have swung to the utilization of home grown solutions for the self-medicine of minor ailments. In any case, numerous phytomedicines require advance examination for their clinical adequacy, while others should be altogether researched for their potential wellbeing dangers or connections with physician recommended drugs.

Phytochemistry is naturally huge by assuming a basic part in the plants to guard themselves against different pathogenic microorganisms by demonstrating the antimicrobial action by hindrance or executing systems. The discharge of these mixes is differing from plant to plant some deliver increasingly and some create in insignificant amount. Now and then they can be unsafe and some of the time they can be exceptionally useful.

Pharmaceutics encompasses a molecular evaluation of drug metabolism and transport processes and the study of genetic, environmental and disease-related factors that regulate or perturb those processes, as well as the fundamental mathematical relationships between enzyme/transporter function, blood concentration-time profiles and the spectrum of pharmacological effects.

Pharmacotherapeutics manages the helpful uses and impacts of medications. Pharmacists are specialists in pharmacotherapy and are in charge of guaranteeing the protected, suitable, and prudent utilization of pharmaceutical medications. As pharmacotherapy masters, pharmacists have duty regarding direct patient care, regularly working as an individual from a multidisciplinary group, and going about as the essential wellspring of medication related data for other social insurance experts. A pharmacotherapy expert is a person who is spent significant time in managing and endorsing medicine, and requires broad scholarly information in pharmacotherapy.

Pharmaceutical formulation is defined as the process in which different chemical substances are combined to produce a final medicinal product. Pharmaceutical formulation is the most frequent method used to achieve slow release and prolong the duration of action of a given drug.

The Pharmaceutical analysis is a branch of chemistry, which involves the series of process for the identification, determination, quantitation, and purification. This is mainly used for the separation of the components from the mixture and for the determination of the structure of the compounds. The different pharmaceutical agents are as follows:

• Plants
• Microorganisms
• Minerals
• Synthetic compounds.

Pathophysiology is the study of the changes of normal mechanical, physical, and biochemical functions, either caused by a disease or resulting from an abnormal syndrome..

Pharmacy Development Services offers independent pharmacy owners profit-generating strategies in operations, business development, data analytics, and many more .The Pharma consultants work with organizations of all sizes including academic institutes, start-up companies, and established organizations. The services aims to increase the patient’s knowledge of their medication and improve their adherence to the regimen. Globally Pharma Market ranges from $870-$900 billion and in Europe $260-$280 billion from which Germany provides ready access to internationally renowned scientists, world-class research and pharmaceuticals markets.

The Pharmaceutical sciences combine broad range of scientific disciplines that are critical to the discovery and development of new drugs and therapies. Pharmaceutical Sciences is a dynamic and interdisciplinary field that aims to integrate fundamental principles of physical and organic chemistry, engineering, biochemistry, and biology to understand how to optimize delivery of drugs to the body and translate this integrated understanding into new and improved therapies against human disease. At the many of institutes internationally recognized faculty contribute to the field through inquiry into the underlying mechanisms of drug interactions with the human body and development of advanced synthetic or biologically-derived materials that can modulate these interactions in pursuit of better and safer therapies and drug products.

The worldwide market for pharmaceutical science instruments and reagents came to $47.8 billion in 2012. This figure is relied upon to increment to $51.3 billion in 2013 and $77.6 billion in 2018, with an anticipated five-year compound yearly development rate (CAGR) of 8.6%.

Drug regulation is the control of drug use by international agreement and/or by regulatory authorities such as the US Food and Drug Administration (FDA), the European Medicines Agency (EMA) and the Japanese Pharmaceutical and Medical Devices Agency (PMDA).

Drug delivery refers to approaches, formulations, technologies, and systems for transporting a pharmaceutical compound in the body as needed to safely achieve its desired therapeutic effect. Drug delivery technologies modify drug release profile, absorption, distribution and elimination for the benefit of improving product efficacy and safety, as well as patient convenience and compliance. Drug release is from: diffusion, degradation, swelling, and affinity-based mechanisms

Pharmaceutical biotechnology is a relatively new and growing field in which the principles of biotechnology are applied to the development of drugs. A majority of therapeutic drugs in the current market are bio formulations, such as antibodies, nucleic acid products and vaccines.

Pharmaceutical engineering is a branch of engineering focused on discovering, formulating, and manufacturing medication, as well as analytical and quality control processes. It utilizes the fields of chemical engineering, biomedical engineering, and pharmaceutical sciences.

Pharmaceutical Microbiology is involves in the study of microorganisms associated with the manufacture of pharmaceuticals e.g. minimizing the number of microorganisms and is a specialist area of microbiology and one concerned with the use of microorganisms in pharmaceutical development and with maintaining contamination control.

Pharmacy practice is the field of pharmacy which involves developing the professional roles of pharmacists. It includes Disease-state management, Clinical drug interventions, Pharmacy professional development and pharmaceutical care, pharmaceutical compounding and health psychology, patient care, drug abuse prevention, prevention of drug interactions or minimisation of adverse events and drug incompatibility and community pharmacy. 

Pharma Companies in Europe - Kowa Pharmaceutical, Aegerion Pharmaceuticals Ltd, Kent Pharmaceuticals, Alan Pharmaceuticals, Alliance Pharmaceutical Limited. Pharmaceutical Companies are knowledge driven industry and is heavily dependent on Research and Development for new products and growth. However, basic research discovering of new molecules is a time consuming and expensive process and is thus, dominated by large global multinationals

Industrial pharmacy is a discipline which includes manufacturing, development, marketing and distribution of drug products including quality assurance of these activities. The research topics are focussed on solving current general problems in pharmaceutical industry, such as formulation and characterisation of sticky amorphous drugs, problem-solving for paediatric medicines and miniaturisation of manufacturing processes.

Physical pharmacy incorporates information of arithmetic, material science and science and applies them to the pharmaceutical dose frame improvement. Physical pharmacy gives the premise to understanding the synthetic and physical wonders that oversee the in vivo and in vitro activities of pharmaceutical items.