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World congress on Pharmaceutical Sciences
Pharma Summit 2019

Theme : Challenges and Prospects in Renovating the Pharma Industry

November 20-21,2019 , Dubai | UAE

Conference Brochure Abstract Submission Organizing Committee Tentative Schedule

About the Conference

Coalesce Research Group invites all the participants from all over the world to attend “World congress on Pharmaceutical Sciences”, scheduled during November 20-21, 2019 in Dubai,UAE mainly focused on the theme “Challenges and Prospects in Renovating the Pharma Industry" .

Pharmaceutical Sciences  offers a best platform with its well organized scientific program to the audience which includes  prompt keynote presentations, Oral talks, Poster presentations, Symposiums, Workshops and Exhibitions. This deals with all the parameters of Pharma research Advances in Anticancer Drug Delivery for tumor targeting ,Drug Delivery Research, Drug Targeting and Design, Know More

Sessions

Click on the session name to expand its sub-sessions.

  •  The Science that deals with the origin, nature, chemistry, effects and uses of drugs; it includes pharmacognosy, pharmacokinetics, pharmacodynamics, pharmacotherapeutics and toxicology. Also the  study of the biochemical and physiological effects of active ingredient on humans.The different parts of pharmacological sciences are Behavioral pharmacology, Medical Pharmacology, Cardiovascular pharmacology, Endocrine pharmacology, Clinical pharmacology, Urogenital pharmacology, Pharmacokinetics, Neuropharmacology, Immune pharmacology.

    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

     

  • The study of drug design to optimize pharmacokinetics and pharmacodynamics, and synthesis of new drug molecules . Pharmaceutical Chemistry is a branch of chemistry that deals with the chemical, biochemical and pharmacological aspects of drugs. It includes synthetic and computational aspects of the study of existing drugs and agents in development in relation to their bioactivities i.e., understanding their structure-activity relationships (SAR).

    The chemical industry is one of the world’s largest branches and has significant influence on many other industries. Total worldwide chemical shipments are worth an enormous five billion U.S. dollars

     

  • Pharmaceutical formulation, in pharmaceutics, is the process in which different chemical substances, including the active drug, are combined to produce a final medicinal product. Formulation studies involve developing a preparation of the drug which is both stable and acceptable to the patient.

    Drug manufacturing is the process of industrial-scale synthesis of pharmaceutical drugs by pharmaceutical companies. The process of drug manufacturing can be broken down into a series of unit operations, such as milling, granulation, coating, tablet pressing, and others.

     

  • Novel drug delivery system (NDDS) involves combining polymer science, pharmaceutics and molecular biology. Novel drug delivery systems are designed based on physical and biochemical mechanisms. The method by which a drug is delivered can have a significant effect on its efficacy. Some drugs have an optimum concentration range within which maximum benefit is derived, and concentrations above or below this range can be toxic or produce no therapeutic benefit at all. NDDS drugs are designed to target the site specific region, in order to achieve desired therapeutic effect, thereby reducing the side or toxic effects. Various drug delivery and drug targeted systems are developed, in order to minimize drug degradation, drug adverse effect, and in order to increase the drug bioavailability (amount of drug available at site targeted region). Site specific drug delivery may be either active or passive process.

     

  • Bio Pharmaceutics plays an important role in drug discovery like drug disposition, Innovations in clinical development, Pharmaceutical technology, Pharmaceutics and drug delivery, Drug design, Targeted drug, gene delivery,  Sustained drug delivery system, Routes of administration, Fundamental drug development

    Pharmaceutical researchers have assessed the relative drug availability to the body in vivo after giving a drug by different routes to an animal or else human, then comparing specific pharmacologic, clinical, or possible toxic responses.

     

  • Pharmaceutical biotechnology can be defined as the science that covers all technologies required for the production, manufacturing and registration of biological drugs Pharmaceutical biotechnology has emerged as one of the major disciplines for drug discovery and development. Today the shape and vision of pharmaceutical aspects and challenges have completely changed, and the prefix "pharma" can also be accepted as a synonym for integrated life science approaches, ranging from genetics to molecular biology to diagnostics, with the common goal of delivering the best drug to the patient by biotechnological techniques.

    Biotechnology plays an important role in pharmaceutical science most especially in the pharmaceutical industries by the creation of genetically modified organisms that can be used in industrial production.

     

  • The process in which different chemical substances, including the active drug, are combined to produce a final medicinal product. The word formulation is often used in a way that includes dosage form. Formulation studies involve developing a preparation of the drug which is both stable and acceptable to the patient. Drug manufacturing is the process of industrial-scale synthesis of pharmaceutical drugs by pharmaceutical companies. The process of drug manufacturing can be broken down into a series of unit operations, such as milling, granulation, coating, tablet pressing, and others.

     

  • Pharmacognosy is the study of drugs derived from Plants and herbs and the other aspect of Pharmacognosy is Phytochemistry Plant preparations are said to be medicinal or herbal when they are used to promote health beyond basic nutrition. The Drugs from natural sources can be obtained by the help of following methods like Computational chemistry, Medicinal chemistry, Molecular drug design, Protein structure prediction, molecular simulation, and exploratory development and Biochemistry.

     

  • Research and Development RD is crucial for the growth and future success of research based Pharma companies to maintain their RD organizations efficient pharmaceutical companies started to hedge the potential of open innovation to cut RD costs and to access external knowledge.
    biopharmaceutical industry invested an estimated $90 billion in research and development (R&D) in 2016. All of PhRMA’s member companies now meet the following criteria ie., A three-year average global R&D to global sales ratio of 10 percent or greater; and A three-year average global R&D spending of at least $200 million per year.
    From drug discovery through FDA approval, developing a new medicine takes between 10-15 years on average and costs an average of $2.6 billion.
     

  • The regulation of drugs varies by jurisdiction. In some countries, such as the United States, they are regulated at the national level by a single agency. In other jurisdictions they are regulated at the state level or at both state and national levels by various bodies, as is the case in Australia.
    Drugs and Regulations are very important in aspects of Pharmaceutical sciences where it deals with Drug safety, Cost effectiveness, Drug rediscovery, Pharmaceutical services, Role of pharmacists, Radio Pharmaceuticals and Multiple drug use etc. 
     

     

  • Nanotechnology is also being applied to or developed for application to a variety of industrial and purification processes. Purification and environmental clean-up applications include the desalination of water, water filtration, wastewater treatment, groundwater treatment, and other Nano remediation.

    The global market for nanotechnology dots was estimated to generate $121.0 million in revenues in 2013. This market is expected to reach about $1.1 billion in 2016 and about $3.1 billion by 2018, at a compound annual growth rate (CAGR) of 90.8% for the five-year period, 2013 to 2018.

     

     

  • The mission of pharmacy education is to prepare graduates who provide patient centered care that ensures optimal medication therapy outcomes and provides a foundation for specialization in specific areas of pharmacy practice; to participate in the education of patients, other health care providers and future pharmacists, to conduct research and scholarly activity and to provide service and leadership to the community.

     

  • The practice of clinical pharmacy embraces the philosophy of pharmaceutical care, blending a caring orientation with specialized therapeutic knowledge, experience, and judgment to ensure optimal patient outcomes.

    Hospital pharmacy is a specialization of this field that includes additional duties such as aiding doctors in applying drug therapy. The statements were developed by the profession to bring uniformity to the practice of hospital pharmacy.

    The overall inpatient and outpatient clinical medication store motorization promote has created to nearly $3.8 billion out of 2016 from $3.5 billion out of 2015. The market is depended upon to create at a five-year compound yearly improvement rate (CAGR) of 7.9% from 2016 to 2021, growing to $5.5 billion of every 2021.

     

  • Clinical trial involves research participants. It follows a pre-defined plan or protocol to evaluate the effects of a medical or behavioral intervention on health outcomes.

    Clinical research aims to advance medical knowledge by studying people, either through direct interaction or through the collection and analysis of blood, tissues, or other samples. By taking part in clinical trials, participants not only play a more active role in their own health care, but they also can access experimental treatments and help others by contributing to medical research.

     

     

  • Pharmacovigilance (PV) is defined as the science and events relating to the detection, assessment, understanding and prevention of adverse effects .WHO established that one Programme for International Drug Monitoring in response to the thalidomide disaster detected in 1961.

    Drug safety is otherwise called Medication Safety in the field of health. 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.

     

     

  • Pharmacogenetics alludes to hereditary contrasts in metabolic pathways which can influence singular reactions to drugs, both as far as restorative impact and additionally antagonistic impacts.
     
    Pharmacogenomics is a quickly creating field that has essential ramifications in individualized treatment for patients and its suggestion influence tranquilize advancement issues such as medication safety, efficiency, and customized health care. Pharmacogenomics consolidates customary pharmaceutical sciences, for example, natural chemistry with explained colleague of qualities, proteins, and single nucleotide polymorphisms.
     

     

Event Venue

Event venue location info and gallery

Dubai, United Arab Emirates

Dubai is a city and emirate in the United Arab Emirates known for luxury shopping, ultramodern architecture and a lively nightlife scene. Burj Khalifa, an 830m-tall tower, dominates the skyscraper-filled skyline. At its foot lies Dubai Fountain, with jets and lights choreographed to music. On artificial islands just offshore is Atlantis, The Palm, a resort with water and marine-animal parks.

Tentative Schedule

Day 1

Time Session
08:30 - 09:00 Registrations
09:00 - 09:30 Inauguration Ceremony
09:30 - 10:30 Keynote Presentations
10:30 - 10:45 Group Photography
10:45 - 11:00 Tea/Coffee & Snacks Break
11:00 - 03:05 Plenary Presentations
13:05 - 14:00 Lunch Break
14:00 - 15:00 Hands on Workshop
15:00 - 15:50 Plenary Presentations
15:50 - 16:05 Evening Break and Networking
16:05 - 18:00 Plenary Presentations

Day 2

Time Session
09:00 - 09:30 On -Spot Registrations
09:30 - 10:30 Keynote Presentations
10:30 - 10:55 Plenary Presentation
10:55 - 11:10 Tea/Coffee & Snacks Break
11:10 - 01:05 Plenary Presentations
12:50 - 13:50 Lunch Break
13:50 - 14:50 Hands on Workshop
14:50 - 16:00 Poster Presentations
16:00 - 16:15 Evening Break and Networking
16:15 - 17:30 Plenary Presentations
17:30 - 18:00 Awards & Closing Ceremony

Registration

Speaker Registration
$ 649

  • Access to all Conference Sessions
  • Opportunity to give a Keynote/ Plenary/ Poster Presentations/ Workshop
  • Opportunity to publish your Abstract in any of our esteemed Journals & in the Conference Proceedings Book
  • Certificate Accredited by our Organizing Committee Member
  • Handbook & Conference Kit
  • Tea/Coffee & Snack, Lunch during the Conference
  •  

Delegate Registration
(No Presentation)
$ 549

  • Access to all Conference Sessions
  • Can meet the Experts of your Area of expertise arriving from 22+ different Countries
  • Participation Certificate Accredited by our Organizing Committee Member
  • Delegates are not allowed to present their papers in Oral or Poster sessions
  • Handbook & Conference Kit
  • Tea/Coffee & Snack, Lunch during the Conference

Student Registration
$ 449

  • Access to all Conference Sessions
  • Opportunity to give an Oral/ Poster Presentation
  • Opportunity to publish your Abstract in any of our esteemed Journals & in the Conference Proceedings Book
  • Certificate Accredited by our Organizing Committee Member
  • Handbook & Conference Kit
  • Tea/Coffee & Snack, Lunch during the Conference
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  •  

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