International Conference on Bio Pharmaceutics December 02-03, 2021 Paris, France

The recent challenges and approach for biosimilars in the biopharmaceutical industry will be discussed. The Clinical studies and the biosimilar innovator in the Pharmaceutical products can be known by the Clinicians for the research in the future of next-generation biosimilar. Another major topic in the pharmaceutical industry Biomarkers in which the recent Biomarker research, development, and technology, measurable parameters for customized therapies will be discussed. The biomarkers are distinguished into Disease-related biomarkers which give an indication of the probable effect of treatment on the patient and Drug-related biomarkers indicate whether a drug will be effective in a specific patient and how the patient’s body will process it. The recent advances and the future scope will be discussed in this global Pharma summit.

Pharmaceutics is the study of relationships between per formulation, pharmaceutical formulation, delivery, disposition, and clinical response. The inherent instability nature of a new drug will alter its desired form into undesired form when presented in a suitable dosage form with the excipients upon storage. In early days this process was confined only for assessing few characteristics, but today this process is being considered as a formulation strategy and hence tremendous technological advancement has been achieved in this field which enables us to save time and money through planned management system and hence impacts. Use of glorious statistical software even based on artificial neural networking is made the task of pre-formulating and optimization process easier. With the increasing number of novel and specialized compounds being developed, a "one size fits all" approach to drug formulation and delivery is no longer optimal, necessitating the consideration of formulations unique to each drug.

Pharma Analytical Techniques are mainly important for manufacturing medicine. Validation process should be done in every technique. Analytical method development and validation, Analytical IQ, OQ, and PQ are to be known in the analysis of the pharmaceutical product. Qualitative & quantitative elemental analysis and the current trends in the gravimetric analysis will be included in the analytical techniques. There are many techniques like UPLC and HPLC techniques, Electroanalytical methods, and Surface characterization techniques for chemical & physical analysis. Pharmaceutical Expo discusses all the analytical techniques and instrumentation that are used for manufacturing medicine.

Good Manufacturing Practice is that part of quality management which ensures that products are consistently produced and controlled according to the quality standards appropriate to their intended use and as required by the marketing authorization, clinical trial authorization or product specification. Current good manufacturing practices guidelines, Current regulations, and quality standards are included. The role of Quality Impact Assessment & effectiveness checks is an essential operation of the pharmaceutical industry. CGMPs provide for systems that assure proper design, monitoring, and control of manufacturing processes and facilities. Management of product storage, transportation and distribution are the major aspects of the GMP practices.

Regulatory affairs also have a very specific meaning within the healthcare pharmaceuticals industries. It includes Regulatory requirements for pharmaceuticals and healthcare products, Intellectual property law for generics and innovator rights. Regulatory requirements for medical devices, Regulatory issues, quality control, and business development and Novel strategies for growth in regulatory affairs are to be discussed. Intellectual property rights are also included.

Clinical Pharmacy includes all the services performed by pharmacists practicing in hospitals, community pharmacies, nursing homes, home-based care services, clinics and any other setting where medicines are prescribed and used. Role of Clinical Pharmacist, Clinical Pharmacy and its key role in treatment can be discussed. Dispensing pharmacy includes the preparation, packaging, labeling, record keeping, and transfer of a prescription drug to a patient or an intermediary. Pharmacotherapy and Environmental health hazards are also discussed.

The innovative Pharmaceutical industry in the United States produces chemically-derived drugs developed as a result of extensive R&D and Clinical trials in both humans and animals.  The innovator relies on patents and other forms of intellectual property rights to justify the investment required to bring a product to market (the U.S. patent term is 20 years).  Several large multinationals produce the majority of innovative pharmaceuticals globally, but they have come to rely more heavily on research performed by industry partners, including smaller, innovative manufacturers.  Pricing of innovative pharmaceuticals is designed to recapture R&D expenditures.

Industrial pharmacy is a discipline which includes manufacturing, development, marketing and distribution of drug products including quality assurance of these activities. The reasons for the increase of large-scale manufacturing Economic – As the scale of manufacturing batches increases so, proportionally, does the cost of production decreases Accuracy – The larger the quantities of materials involved so, proportionally, is the accuracy of measurements increased.

Pharmaceutical nanotechnology has provided more fine-tuned diagnosis and focused treatment of disease at a molecular level. Pharmaceutical nanotechnology is the most innovative and highly specialized field, which will revolutionize the pharmaceutical industry in the near future. Pharmaceutical nanotechnology presents revolutionary opportunities to fight against many diseases. It helps in identifying the antigen associated with diseases such as cancer, diabetes mellitus, neurodegenerative diseases, as well as detecting the microorganisms and viruses associated with infections. It is expected that in the next 10 years the market will be flooded with nanotechnology devised medicine.

Medicinal chemistry and pharmaceutical chemistries are disciplines at the intersection of chemistry, especially synthetic organic chemistry, and pharmacology and various other biological specialties, where they are involved with design, chemical synthesis and development for the market of pharmaceutical agents, or bio-active molecules (drugs). Current developments in medicinal chemistry, Diagnostic and bioinorganic medicinal chemistry are to be discussed. It includes Green techniques for organic synthesis and medicinal chemistry. 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. It includes Advances in Drug discovery, recent advances in fluorinated pharmaceuticals based on natural products. Plant and microbial derived drugs in Drug discovery are also discussed.

Pharmacognosy and Photochemistry will be discussed to impart knowledge of alternative systems of medicine as well as modern Pharmacognosy. The drugs from natural products, crude drugs, and plant products its availability and toxicological studies are discussed. Pharmacognosy practice in the industry and the documentation procedures for herbal drugs are important to know according to the guidelines. Photochemistry is the study of phytochemicals and the subfield of Botany and Chemistry. The Analytical Techniques and Constituents elements in the photochemistry (Phyto constituents) are the major topic to be known in the field of photochemistry. It would serve as a valuable resource of information to other botanical and healthcare science students, researchers and industrialists in the field of herbal medicine. So the delegates from the field of Pharmacognosy and Photochemistry from all over the world can attend this Pharmaceutical Expo India to explore the Research.