September 17, 2020    London, UK

2nd webinar on Personalised Medicine and Pharmacovigilence

September 17, 2020

2nd webinar on Personalised Medicine and Pharmacovigilence

Exploring Advances of COVID-19 in Personalized Medicine and Pharmacovigilence
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Briefly Know About This Event

Webinar on Personalized Medicine and Pharmacogenomics will be hosted on September 17th, 2020 in London, UK (GMT+4). Panel of speakers will be delivering their presentations on their recent research related to  Health care, Medicine, Genomics and Pharmacovigilence. Current state of knowledge, its impact on future will be discussed in detailed. Longdom invites all experts to be part this webinar series and make it a perfect platform for knowledge sharing and networking.

webinar cordially invites Researchers, Physicians, Genomics associations, Public Healthcare Professionals and Pharmacovigilance Professionals from all over the globe to be present at the webinar and it is going to be an extraordinary event which will focus on the recent medical developments in the fields of Personalized Medicine, Personalized drug base on the theme “Exploring Advances of COVID-19 in Personalized Medicine and Pharmacovigilence


Personalized Medicine is a multi-faceted way to deal with patient consideration that not just improves our capacity to analyze and treat illness, yet offers the possibility to identify sickness at a prior stage when it is simpler to treat adequately. The Personalized drug gives a chance to create operators that are focused on patient gatherings that don't react to prescriptions as proposed and for whom the conventional wellbeing frameworks have generally fizzled. The fruitful routine with regards to Personalized medication requires changes by and by examples and the board methodologies for social insurance experts just as for producers in repayment, administrative practices and information sharing.

Pharmacovigilance and Clinical Trials will have the fast development of new drug and innovative therapeutics, new pharmacovigilance actions and methods have to be implemented for assurance and Patient Benefit Safety Management in Pharma, Biotech and Health Care. Clinical Trails contain the best quality level to calculate the viability and wellbeing of new medications. However, in light of the fact that they are directed in homogeneous conditions a long way from this present reality of solution and use, errors in patient choice or treatment situations may change both the viability and risks.

Drug absorption is a pharmacokinetic parameter that refers to the way a drug is absorbed from a pharmaceutical formulation into the bloodstream.  The rate of absorption depends upon the ratio of the 2 forms at a particular site and is also a factor in circulation and elimination. Drug safety relates to the potential for adverse effects related to the administration of drugs. Efforts to establish the safely profile of drugs begin early in their development, with in vitro and in vivo toxicity testing, and continue through clinical trials leading up to drug approval and following approval in specific post-marketing studies or general pharmacovigilance efforts.

Precision Medicine is a rising methodology for infection treatment and counteractive action that considers singular fluctuation in qualities, condition, and way of life for every individual. This methodology will enable specialists and scientists to anticipate all the more precisely which treatment and avoidance techniques for a specific illness will work in which gatherings of individuals. Vaccinology is to determine and develop extremely immunogenic and safe vaccines that protect against infectious and non-infectious i.e., cancers diseases but it is failure till date because of both pathogen and host variability. For hyper-variable viral pathogens like HIV, HCV and rhinovirus it has been unable to discover and develop highly immunogenic vaccine.

Drug tolerance is revealing of drug use but is not necessarily associated with drug dependence or addiction. The process of tolerance development is reversible that can involve both physiological factors and psychological factors. Adverse drug reactions can be considered a form of toxicity .toxicity is most commonly applied to effects of over absorption. For information on toxicity of specific drugs see the table Symptoms and Treatment of Specific Toxins. Adverse drug reactions are usually classified as mild, moderate, lethal (see table Classification of Adverse Drug Reactions.



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