Drug formulation Webinars 2021|Drug formulation Conferences 2021|Drug Delivery online events |Drug formulation Congress| Drug Delivery |Pharmaceutical webinar

Theme: Drug Development, Formulation and Combination to overcome the Covid-19 Disease Outbreak

DRUG FORMULATION CONGRESS 2021

DRUG FORMULATION CONGRESS 2021

18^th World Congress on Drug Formulation & Drug Delivery is scheduled to be held during May 04-05, 2021 Online Webinar Event with the theme "Drug Development, Formulation and Combination to overcome the Covid-19 Disease Outbreak". This Pharmaceutical webinar 2021 includes a wide range of Keynote presentations, plenary talks, symposium, Workshops, Exhibitions, Poster presentations and Career development in Pharmacy.

Why to Attend???

DRUG FORMULATION CONGRESS 2021 webinar is a multidisciplinary program with broad participation with members from around the globe focused on learning about drug formulation and drug delivery and its advances. This is your best opportunity to reach the largest assemblage of participants from Pharmacy research community that is from academia in the DRUG FORMULATION CONGRESS 2021, drug delivery entities, medical groups, related associations, societies and also from government agencies, pharmaceutical, biomedical and medical device industries.

Drug Formulation Congress 2021 will discuss various disciplines involved in the drug formulation procedures and Novel Drug Delivery Conferences; it will educate health care researchers about drug formulation and drug design, operation, organizing, research computing Regulatory aspects` and reporting of formulations. This conference conduct presentations, distribute information, meet with current and potential scientists, make a splash with new Pharmacy Research developers in Pharmacy and receive name recognition at this 2-days event. World renowned speakers and the most recent techniques, developments, the newest updates in formulations and drug delivery are hallmarks of this Pharmacy.

Who should attend and Who You’ll Meet

Directors/Senior Directors/Executive Directors and Vice Presidents/Senior Vice Presidents/Executive Vice Presidents and Heads/Leaders/Partners of

• CROs and CMOs

• Pharmacy Research Sites

• Pharmacy/Biotech and Medical Device industries

• Hospitals, Associations

Pharmaceutical Conferences 2021, Drug Formulation Congress 2021, Novel Drug Delivery Congress, Medical Directors, Principal Investigators, Methodologists, and other Drug Formulation Experts, Drug Formulation Professors, Drug Formulation Graduates, Pharmacy in Pharmacy along with Academicians: University Faculties like Directors, Senior Professors/Assistant Professors/ Associate Professors, Research Scholars, scientists who are related to drug formulation pharmaceutical research.

Target Audience

PhD Scholars in Drug Formulation
PhD in Pharmaceutical Sciences
Graduates and Post Graduates in Pharmaceutics
Pharmaceutical Science Professors, Associate Professors, Assistant Professors
Bio instruments Professionals
Bio-informatics Professionals
Directors, CEO’s of Organizations
Supply Chain companies
Pharmaceutical Manufacturing Companies
Software development companies
Drug Formulation Research Institutes and members

1. Drug Design & Development

Pharmaceutical Conferences 2021 describes drug design is the approach of inventing revolutionary medicines. Drug design and Drug formulation defines the design of molecules that are corresponding in form and price to the bio molecular target with which they interact and consequently will bind to it. Generally, the drug is a tiny organic molecule which triggers or slows down the activity of a bio-molecule consisting of a protein which time and again results in a medicinal gain to the patient. Discovery of drugs and Drug formulation is hard. Various medicinal drugs are invented by chance observations, the scientific examination of other drug treatments or by finding out the facet consequences of a few different tablets. A methodical method is large screening observations in which vital drug objectives are examined with hundreds of diverse compounds to take a look at, whether conversations occur. Basically, Drug Formulation and drug layout includes drug design of small molecules that are harmonizing in form and fee to the bio molecular target to which they act collectively and consequently will bind to it.

1. Current problems in Pharmacovigilance

2. Adverse drug reactions with Pharmaceutical products

3. Detection and evaluation of drug safety signals

4. Improve Pharmacovigilance through Patient and Provider Education

2. Computer Aided Drug Design (CADD)

The strategies of designing a new drug by using bioinformatics implements have opened a brand new location of drug research and development. Computational techniques help us in searching drug target and in Drug Formulation designing drug. Pharmaceutical Conferences 2021, Bioinformatics impacts drug formula and new drug layout in the following drug design path.

By the use of computational methods and the 3D structural statistics of the protein target, we are now able to scrutinize the distinct underlying molecular and atomic interactions worried in ligand: protein interactions and consequently interpret experimental effects in element. The use of computer systems in drug system and drug discovery bears the additional benefit of delivering new drug candidates more hastily and cost-correctly. Computer-aided drug discovery has lately had crucial successes in drug formulae.

3. Biomarkers in Drug Design

Tech Association of British Pharmaceutical Industry, Indian Society for Clinical Organization Researcher advancements in the molecular characterization of cancers have assisted researchers to discover increasingly more key molecular drivers of most cancers progression. These drug discoveries have caused a couple of novel anticancer therapeutics, and scientific advantage in decided on affected person populations. Despite this, the identification of clinically relevant predictive biomarkers of reaction continues to lag in the back of. In this review, we speak strategies for the molecular characterization of cancers and the importance of biomarkers for the development of novel antitumor therapeutics.

The discovery and assessment of any novel biomarkers will ideally be specialized to Clinical Laboratory Improvement Amendments (CLIA) and Good Clinical Laboratory Practice (GCLP) standards, with the intention to ensure accuracy and reproducibility of laboratory processes. Predictive biomarkers suggest the likelihood of response to a specific antitumor therapy. Such assays should be scientifically sound, Predictive biomarkers consist of each tumour-unique and surrogate biomarker and are essential to accelerating the drug development process.

Regulatory Prospects in BRIC countries
Product Similarity for Biosimilars & Analytical Challenges
Role of Medical Affairs in Biosimilars
Regulatory strategy for generics and Biosimilars

4. Pre-Formulation & Formulation Aspects

Drug Formulation is the observe of relationships among pre-gadget, pharmaceutical components, transport, disposition and scientific response. The inherent instability nature of a new drug will adjust its desired shape into undesired shape at the same time as furnished in a suitable dosage shape with the excipient/s upon garage. In early days this gadget changed into restrained simplest for assessing few traits, however these days this system is being taken into consideration as a method strategy and consequently first-rate technological development has been finished in this subject which enables us to keep time and money through planned control tool and consequently influences Drug Formulation 2017 to be a Drug Formulation Conferencev. Use of splendid statistical software program software even based on artificial neural networking are made the mission of pre-method and optimization system simpler. Role of pre formulation studies strategies like freeze drying elements duties the occasion Drug Formulation 2017 to pose as a freeze drying meeting in drug discovery, drug development performs essential function in pharmaceutical drug system improvement and the revisions will help in one-of-a-type dosage paperwork layout.

Regulatory updates and key drivers for registration
Biowaiver approval for Biosimilars
Generic Biosimilars
Regulatory Prospects in BRIC countries

5. Pharmacokinetics & Pharmacodynamics

Pharmacokinetics is presently defined because the take a look at of the time course of drug absorption, distribution, metabolism, and excretion. Clinical pharmacokinetics is the utility of pharmacokinetic principles to the secure and powerful healing management of medicine in a man or woman patient. Primary desires of clinical pharmacokinetics and drug formula consist of enhancing efficacy and lowering toxicity of a affected person’s drug remedy. The improvement of sturdy correlations between drug concentrations and their pharmacologic responses has enabled clinicians to apply pharmacokinetic principles to actual affected person conditions.

Pharmacodynamics refers to the relationship among drug attention at the web site of motion and the ensuing impact, such as the time route and intensity of therapeutic and unfavourable consequences. The effect of a drug gift on the site of achievement is decided by means of that drug’s binding with a receptor.

· Analysis of the Biosimilar Development Pipeline
· Legal Issues and Implementation of the BPCI Act
· Pharma patent scenario

6. Clinical Trials & Bio therapeutics

Clinical Bio therapeutic factors inclusive of have a look at drug formulations, drug layout, drug-drug interactions, QT evaluation, immunogenicity, comparison, special populations (hepatic and liver failure), PK and PD, regulatory expectancies of PK and PD characterization, as well as reviewing factors which impact the ADME of Bio therapeutics. The objectives of early scientific improvement of healing proteins are similar to for small molecules .i.e. To investigate the molecule in a manner with the intention to gain important knowledge approximately its tolerability safety pharmacokinetics (PK) and if possible pharmacodynamics (PD) consequences in the most suitable human populations even as simultaneously protecting their protection. However, there are unique features of proteins that ought to be considered while designing scientific pharmacology studies.

Biosimilar Product Reimbursement and Pricing
Biosimilar Regulatory Updates and Legal Implications
Biosimilar Market Access and Commercialization

7. Innovative Drug Discovery and Nanotechnology

Size reduction is a fundamental unit operation having critical packages in Pharmaceutical Sciences, Drug Formulations. It enables in enhancing solubility and bioavailability, decreasing toxicity, enhancing release and providing better drug components possibilities for capsules. In maximum of the instances, size discount is limited to micron size variety, for instance, numerous pharmaceutical dosage forms like powder, emulsion, suspension etc. Drugs in the Nano meter size variety beautify overall performance in an expansion of dosage paperwork.

Pharmaceutical nanotechnology has provided greater pleasant-tuned diagnosis and focused remedy of ailment at a molecular stage. Pharmaceutical nanotechnology is maximum progressive and quite specialized field, for you to revolutionize the pharmaceutical industry in close to destiny.

Criteria for patentability and patent claims
Critical research issues
Patentable subject matter
Recent patent disputes and litigations

8. Novel Drug Delivery System

Identifying drug objectives plays critical roles in designing new drugs, drug formulations and combating illnesses. Unfortunately, our cutting-edge expertise about drug objectives is a long way from comprehensive. Screening drug goals within the lab is a luxurious and time-ingesting technique. In the past decade, the accumulation of diverse forms of study of technology associated statistics makes it viable to expand computational strategies to are expecting drug targets. Non-communicable diseases together with most cancers, atherosclerosis and diabetes are answerable for maximum important social and health ache as hundreds of thousands of people are loss of life each year. Out of which, atherosclerosis is the main purpose of deaths international.

Current problems in Pharmacovigilance
Adverse drug reactions with Pharmaceutical products
Detection and evaluation of drug safety signals

9. Medicinal Chemistry & Drug Discover Advancements

Medicinal Chemistry is a branch of chemistry which particularly agreements with artificial natural chemistry and pharmacology inclusive of diverse other organic specialties that's worried with design. It combines information and capacities from the fields of cheminformatics, molecule, chemical advent and development of drug for advertising and marketing of pharmaceutical agents lard modelling and crucial bioinformatics and drug formulations, needs an in-depth appreciative of the physic-chemical houses of a three-dimensional molecule.

10. Drug Product Manufacturing

Drug manufacturing (Pharmaceutical Manufacturing) is the manner of industrial-scale synthesis of pharmaceutical drugs with the aid of pharmaceutical agencies. The manner of drug formulations may be demolished down into a series of unit operations, along with milling, granulation, coating, tablet pressing, and others. The changing pharmaceutical panorama is a popular discussion point as of late. Armed with a clean, non-blockbuster-reliant commercial enterprise version and remedy alternatives that are expanding from small molecules to a variety of new, greater cantered cures, the industry is at what PwC calls, “a critical juncture.” Parenteral drug delivery, Novel Drug Delivery is the second largest segment of this transformative pharmaceutical market covered only by the more mature oral solid dosage forms accounting for nearly 30% of total Parma market share. According to Survey, the market for parenteral drug delivery products is projected to rise over 10% annually to $86.5 billion in 2019.

11. Chemical and Pharmaceutical Engineering

Pharmaceutical engineering is a branch of pharmaceutical technology and science that involves improvement and production of products, techniques, and additives within the pharmaceuticals industry (i.e. drugs & biologics). While developing pharmaceutical merchandise includes many interrelated disciplines (e.g. medicinal chemists, analytical chemists, clinicians/pharmacologists, pharmacists, chemical engineers, biomedical engineers, etc.), the precise subfield of "pharmaceutical engineering" has most effective emerged recently as a divergent engineering discipline. This now brings the trouble-solving standards and quantitative education of engineering to complement the opposite scientific fields already worried in drug formulations

12. Business Opportunities in Drug Delivery

The global market for Business Development of Drug Delivery Technology in 2010 was $131.6 billion and is expected to rise at a compound annual growth rate (CAGR) of 5% and reach nearly $175.6 billion by 2016. The U.S constituted approximately 59% of the total drug delivery market in 2010 and was $78 billion. It is forecast to reach nearly $103 billion in 2016 at a CAGR of 4.7%. Europe contributed about 27% of the total drug delivery market in 2010 and was $36 billion and is expected to grow to $49 billion by 2016 at a CAGR of 5.6% in 2013, Drug Delivery Global market reached $150.3 billion, according to BCC research. This was an increase from $142 billion the previous year. Given its predicted annual growth the market represents a considerable business opportunity, which has been reflected in increasing number of drug delivery specialists. Consistent quality and competitive costs of product improves Production performance and continuity of supply and Product and technology auditing and due diligence with minimizing Regulatory Issues, drug formulation, quality control, and business development Business opportunities in drug delivery.

Drug Formulation and Drug Delivery Conference will discuss effective formulation and delivery technologies for enhancing solubility and drug delivery. Drug Formulation Congress 2018 aims to aggregate leading experts from around the world who will discuss on formulation and delivery, and show how they are developing poorly soluble drugs into scientifically sound, patient-centric formulations, and reducing their product development timelines.

Active Pharmaceutical Ingredient Market:

Transparency Market research states the opportunity in this market will be worth US$219.60 bn by 2023 from US$134.7 bn in 2015. Between the forecast period of 2015 and 2023, the overall market is expected to expand at a CAGR of 6.3%. Between the forecast period of 2015 and 2023, the overall market is expected to expand at a CAGR of 6.3%.

The global pharmaceutical excipients market is projected to reach USD 8.1 Billion in 2021 at a CAGR of 6.1% in the forecast period 2016 to 2021. The rising demand for new drug delivery systems, greater understanding of the functional benefits of excipients, growing pharmaceutical industry, and patent expiries of several blockbuster drugs are positively impacting the overall growth of the market

Allergan Pharmaceuticals Pty. Ltd

Baxter Healthcare Ltd.

CSL Biotherapies (NZ) Ltd

Douglas Pharmaceuticals

GlaxoSmithKline

Janssen-Cling Pty Ltd.

Merck Ltd

Neuron Pharmaceuticals Limited

Novartis New Zealand Ltd

Novo Nordisk Pharmaceuticals Ltd

ORGANON New Zealand

Pharmacy NZ Ltd

PSM Healthcare Ltd

Roche Products NZ Ltd.

Roche Products NZ Ltd

Major Associations around the Globe:

Pharmaceutical Research and Manufacturers of America

Regulatory Affairs Professionals Society

International Society of Pharmaceutical Compounding (ISPhC)

International Young Pharmacists' Group (YPG)

Parenteral Drug Association (PDA)

Regulatory Affairs Professionals Society (RAPS)

Controlled Release Society

Society for biomaterials

Washington State Pharmacy Association

Inhalation Drug Delivery Association

New Education Group (part of ACG Education)

Conference Highlights

To share your views and research, please click here to register for the Conference.

To Collaborate Scientific Professionals around the World

Conference Date	May 04-05, 2021
Sponsors & Exhibitors	~~Click here for Sponsorship Opportunities~~
Speaker Opportunity Closed
Poster Opportunity Closed	Click Here to View

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Special Issues

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

Abstracts will be provided with Digital Object Identifier by

18^th World Congress on Drug Formulation & Drug Delivery May 04-05, 2021 Bangkok, Thailand

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DRUG FORMULATION CONGRESS 2021

Conference Highlights

To Collaborate Scientific Professionals around the World

Useful Links

Special Issues