i-Pharma 2022, 3rd International Pharmaceutical Conference and Expo
Start
Thu, 29 Sep 2022, 09:00
End
Fri, 30 Sep 2022, 18:00
Venue:
Exhibit
Symposia
Workshops
Organiser
Sponsor
3rd International Pharmaceutical Conference and Expo welcome you as our guest to London, UK on May 09-10, 2022. i-Pharma 2022 includes nearly every permutation of knowledge, innovation, technology, and networking; and has the objective of creating an international forum for academicians, practitioners, and business professionals to discuss the soundest issues related to Pharma, Biotech, and Health Care.
This program provides two days of robust discussions in the field of Drug Discovery and Development, Pharmacovigilance and Drug Safety, Novel Drug Delivery Systems and Drug therapy, Pharmaceutical Nanotechnology, Drug Regulatory Affairs, Pharmacology, Neuropharmacology, Nutraceuticals, Pharma Marketing, Orphan and Rare Disease and more.
i-Pharma 2022 offers unparalleled business, research opportunities, and access to new markets in Pharma and Health Care industry. Be on the cutting edge of new and often yet-unreleased information and discover an area that piques your interest.
Join us and witness the booming industry by participating at i-Pharma 2022 and give your career and business access to new opportunities from throughout the world.
The US pharmaceutical market consists of majorly two types of drugs, i.e. traditional drugs and specialty drugs. Specialty drugs are meant for chronic and rare diseases and have gained a strong foothold in recent times. The specialty market has changed over the years with a lot of these drugs being in their final phase of development and is likely to have staggering growth due to factors like an aging population, improving life expectancy and a rise in net per capita. The factors that affect the pharmaceutical market size include disease prevalence, drug affordability, government policies, and some supply-side factors. Biotech drugs include a wide range of products such as therapeutic proteins, vaccines, blood and blood components, tissues, etc. are revolutionizing the treatment of autoimmune disorders and cancer, and are critical to the future of the industry. Drugs are subjected to a variety of laws and regulations that govern the patenting, safety, testing, and efficacy of drugs. With the sequencing of the human genome, clinical research in potential new drug therapies is likely to increase further. Sound drug regulatory regulations provide the foundation for the ethos of drug safety, and for public conviction in medicines.
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