征稿已开启

查看我的稿件

注册已开启

查看我的门票

已截止
活动简介

Conference Series LLC invites all the participants across the globe to attend 12th World  Pharma Congress during October 16-18, 2017 Budapest, Hungary. Which includes prompt keynote presentations, Oral talks, Poster presentations and Exhibitions. Pharma Congress 2017 is a specially designed cluster Pharma conference. The main theme of this Pharma conferences is “Current Technologies & Advancements In Pharmaceutical Field’’. The Impact of developing and Marketing Drugs, its Registration & Approval” which covers a wide range of critically important sessions. 

Why to Attend???

Meet Your Target Market with members from around the world focused on learning about Pharma, this is your single best opportunity to reach the largest assemblage of participants from the Pharma community. Conduct demonstrations, distribute information, meet with current and potential Scientists, make a splash with a new research, and receive name recognition at this 3-day Pharmaceutical Event.World-renowned speakers, the most recent techniques, tactics, and the newest updates in Pharmaceutical Sciences fields are hallmarks of this conference.

A Unique Opportunity for Advertisers and Sponsors at this International event:

Target Audience:

  • Professors, Associate Professors, Assistant Professors

  • PhD Scholars

  • Graduates and Post Graduates

  • Directors, CEO’s of Organizations

  • Association, Association presidents and professionals

  • Noble laureates in Health Care and Medicine

  • Bio instruments Professionals

  • Bio-informatics Professionals

  • Software development companies

  • Research Institutes and members

  • Supply Chain companies

  • Manufacturing Companies

  • CRO and DATA management Companies

  • Training Institutes

  • Business Entrepreneurr

Market Analysis

Over the last few decades a great deal of progress has  increased in research oriented approaches like improved technologies, developed infrastructures, and increased research in the field of Drug discovery, clinical trials, Drug delivery, preformulation studies and Nano-medicine in the pharmaceutical industry. To develop a new pharmaceutical formulation and to conduct clinical trials it cost at € 1,926 million in 2016. The global pharmaceutical excipients market is projected to reach USD 8.1 Billion in 2021. The new drug delivery system demand is increasing due to greater understanding of the functional benefits of excipients, pharmaceutical industry growth, and patent expiries of several popular drugs are positively impacting the overall growth of the market.

Revenue of the worldwide pharma market in 2016 was $1072bn. The global pharmaceutical industry was worth $10613bn in 2015. The generic pharma industry is currently worth an estimated $ 225 billion US and the largest four generic pharma companies worldwide by sales (Teva, Sandoz, Mylan, & Watson) account for nearly 50% of generic prescriptions in the US and 40% worldwide. The United Sates is a major hub for drug manufacturing and its market imports were valued over $86 billion in 2016, making the world’s largest importer of pharmaceuticals and $47 billion exports.

According to the 2015 EU Industrial R&D Investment Scoreboard the pharmaceutical and biotechnology sector amounts to 18.2% of total business R&D expenditure worldwide.On the other side Europe drug manufacturing is 225000 €millions and exports were 361500 €millions. Europe spent 31,500 €millions on R&D in 2015 while US spent 47,061€millions.However, considering the all aspects the European pharma market is expected to grow by 27% between 2015 and 2022.

Germany is forecast to have highest increase in market value at € 11.4bn. Novartis is forecast to reduce its R&D spending, from $10.5bn in 2020 to only $9.2bn in 2022. Of the top 20, Celgene and Regeneron are forecast to grow their R&D expenses most rapidly, with R&D spend forecast to increase 11% per year until 2022. Overall, total R&D spends is expected to increase by 2.8% each year, reaching $182bn in 2022.

Patient awareness regarding adverse drug events is stimulating global pharmacovigilance market growth by increase in number of National pharmacovigilance centers. Spain pharmacovigilance market size was valued over USD 230 million in 2015 and witness 10.2% CAGR from 2016 to 2024, to surpass USD 550 million by 2024.

Drug discovery technologies study includes Bio analytical Assays, Bioinformatics, Cell Based Assays, Genomic Technologies, High Throughput Screening, Proteomic Technologies and Others comprising Epigenetics, Metabolomics, Combinatorial Chemistry, Synthetic Biology, Systems Biology and Nanotechnology. The global market value for these technologies market with an expected share of about 30% in 2015 valued at $18 billion followed by Bioanalytical Assays or instruments by about $14 billion.

Innovative formulations are estimated to have contributed to 73%. Biopharmaceuticals have set new standards for popular drugs, which are traditionally defined as drugs that have $1 billion or more in annual sales; the top 15 biopharmaceutical products each profits annual revenue of more than $2 billion, with some drugs generating sales of more than $10 billion a year. In 2015 the top NMEs include Pfizer’s Ibrance, J&J’s Darzalex and Gilead’s Genvoya with a cumulative value of $32bn of sales expected in 2020. The increasing number of breakthrough therapy approvals also proves the ability of the pharmaceutical R&D to offer incremental benefits to targeted patient segments with larger unmet needs.

征稿信息

征稿范围

Pharmaceutical Sciences

  • Biopharmaceutics

  • Physical Pharmaceutics

  • Pharmacology

  • Pharmacogenomics

  • Bio informatics

  • Pharmaceutical Microbiology and Sterilization

  • Pharmacognocy

  • Pharmaceutical Jurisprudence

  • Organic and Inorganic Chemistry

  • 0Pharmaceutical Botany

  • Pharmacoepidemiology

Drug Discovery & Research

  • Nanotechnology

  • Genomic Technologies

  • Proteomic Technologies

  • Synthetic Biology

  • Quality by Design

  • Random Screening

  • Molecular Designing

  • Drug Metabolites

  • Challenges in Drug Discovery

  • 0Criteria for Target Selection

  • Advancements of In vitro studies

  • Enhancements of In vivo studies

Drug Therapy

  • Effective ways of Drug Therapy

  • Adverse Effects in Drug Therapy

  • Drug therapy problem for seamless

  • Drug Therapy Monitoring

  • Therapeutic index

Advances in Clinical Trials

  • Role of Clinical Trials

  • Goals of Preclinical studies

  • Safety potential results of Preclinical studies

  • Overcoming hurdles in Clinical Trials

  • Meeting the requirements of FDA review process

  • Safety and Effectiveness of Drug

Drug Delivery Systems

  • Nano Drug Delivery Systems

  • Polymeric Drug Delivery Systems

  • Drug Metabolites Novel Drug Delivery

  • Transdermal Drug Delivery System

  • Protein-Protein Interactions as Drug

  • Recent Trends in Drug Delivery

Pharmaceutical Drug Formulations

  • Drug selection

  • Preformulation studies

  • Types of Dosage forms

  • Polymeric Drug Formulation

  • Surface and Bulk Properties of Polymers

  • Advances in improvement of formulations in Route of Administration

  • Advanced Evaluations in Product Efficacy

  • Nano-pharmaceutical formulations

  • Pharmaceutical Devices

Innovations in Drug Development

  • Innovative Therapeutic Studies

  • Effect of Polymorphism in Pharmaceutical Drug Development

  • Technical limitations in Drug Development

  • Difficulties in Regulatory Approvals

  • Financial constraints in Drug Development

Regulatory Affairs & Intellectual Property Rights

  • Regulatory Affairs Filing and Documenta

  • Enhancing Regulatory Science for Public

  • Meeting the Challenges for Regulating

  • Patent and types of Patent Application

  • Copyrights

  • Trademark

  • Infringement

  • Iprs and Market for Technology

  • Role of Patent Co-operation Therapy

Pharmacovigilance

  • Adverse Event Reporting

  • Risk Management Plans

  • The Importance of Pharmacovigilance, Safety Monitoring

  • Role of Pharmacovigilance Centres

  • Ecopharmacovigilance (EPV: pharmacoenvironmentology)

Good Manufacturing Practices

  • Good Manufacturing Practice in International Countries

  • GMP Requirements & Medical devices

  • GMP Guidelines

  • Technology in GMP and cGMP

  • Pharmaceutical cGMPs for the 21st Century: A Risk-Based Approach

Ethics In Pharmacy

  • Pharmacist in Relation to his Job

  • Pharmacist in Relation to his Trade

  • Pharmacist In Relation to his Medical Profession

Pharmacy & Pharmacist

  • Challenges in Pharmacy Practise

  • Role of Pharmacist in Patient Care

  • Role of Pharmacist in the Future

  • Future Vision and Challenges for Hospital Pharmacy

  • Challenges in Pharmacy Supply of Medicine to the Provision of Care

  • The Impact of Technology in Pharmacy

  • Role of Pharmcay in Development and Needs of Patient Care

  • Trends and Problems in Posology

Drug Disposition & Biological Products

  • Drug Absorption Methods

  • Effect of pH on Drug Disposition

  • Drug Distribution

  • Drug Metabolism

  • Drug Excretion

  • Biologics and Biosimilars

Pharmaceutical Analysis

  • Qualitative Analysis

  • Quantitative Analysis

  • Quality Control and Quality Assurance

  • Validation Methods

Pharma Marketing

  • Role of Pharmaceutical Representatives

  • Evaluation of Marketing

  • Regulation and Fraud

  • Cost Effectiveness of Medicines (Pharmacoeconomics)

Bio-avilability and Bio-equivalence

  • Physico - Chemical properties affecting Bioavailability

  • Formulation Factors Aaffecting Bioavailability

  • Pharmacokinetics

  • Pharmacodynamics Studies

Entrepreneurs Investment Meet

作者指南

All accepted abstracts will be published in respective Conferenceseries International Journals.

留言
验证码 看不清楚,更换一张
全部留言
重要日期
  • 会议日期

    10月16日

    2017

    10月18日

    2017

  • 10月18日 2017

    注册截止日期

移动端
在手机上打开
小程序
打开微信小程序
客服
扫码或点此咨询