Recommended Global Pharmaceutical Sciences Conferences
Drug Formulation 2018
Sessions & Tracks
ConferenceSeries Ltdis very delighted to invite you all to the "10th Annual Congress on Drug Formulation & Analytical Techniques" ( Drug Formulation 2018) scheduled on September 24-25 , 2018 at UAE, Dubai. Conference Series Ltd organizes conference series of 3000+ Global Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops in USA, Europe & Asia with support from 1000 more scientific societies and publishes 700+ Open access journals which contains over 30000 eminent personalities, reputed scientists as editorial board members.
ConferenceSeries Ltd is a world class conference organizer, which have highly talented conference organizers around the globe. We have 70,000 editorial board members for ConferenceSeries Ltd journals and also 600+ Scientific conferences. We publish more than 700+ Open access journals for which we have more than 1 million readers and we strictly follow 21 day rapid review process. We endeavor to support and organize a variety of conferences throughout the year as educational opportunities to update knowledge and skills. To know more about the conference series visit: http://www.conferenceseries.com/
Track 1: Pharmaceutical Formulations
Pharmaceutical formulation in pharmaceutics is the process in which various chemical substances including the vigorous drug are joined to produce a final medicinal product. Formulation studies involve developing a preparation of the drug which is both stable and acceptable to the patient. For orally taken drugs, this usually contains combining the drug into a tablet or a capsule. Formulations confirm that the drug is compatible with these other substances. In the pharmaceutical drug formulations, the different physical, chemical, and mechanical properties of a drug are considered so as to know what other ingredients should be used in the preparation. The various factors like polymorphism, particle size, pH, and solubility are all considered while formulating the drug, also considering the appearance of the tablet.
Track 2: Drug Formulation Procedures
The drug subjected to drug development undergoes number of trials and are screened at different stages to produce a final potent drug intended for the treatment of various diseases. During this process various properties are checked to see whether the drug is non-toxic to living system and is therapeutic or not. Using suitable excipients and technological preparations the active substances are formulated into final dosage form. The last product is the Actual composition of preparation, manufacturing specification.
Bioavailability is a subcategory of pharmacological absorption. Bioavailability is generally assessed by finding the area under the plasma concentration–time curve. The factors affecting bioavailability are Pharmaceutics factors, physicochemical properties of drug, Dosage form characteristics & Pharmaceutic Ingredients, Patient related factors like age, Routes of administration (Parenteral, Rectal, Oral, and Topical) etc.
Conducting a BA study enables assessment of the impact of route of administration on BA and defines the absolute BA of the drug released from the drug product. BA for a given formulation provides an assessment of the relative fraction of the orally administered dose that is absorbed into the systemic circulation. If the reference standard is an IV dose, it is referred as Absolute Bioavailability. If the reference standard is any other dosage form than IV it is referred as Relative Bioavailability.
Track 4: Drug & Forensic Toxicology
The primary scope of toxicological studies in the drug development process is to estimate the safety of potential drugs. This is proficient using relevant animal models and validated procedures. The ultimate goal is to translate the animal model responses into an understanding of the risk for the human subjects. The drug toxicology plays a very important role in evaluating the safety of the drug.
Industrial Pharmacy also plays a crucial role in any drug discovery. To any novel drug discovery the industrial approach is very important to get massive commercial application. Few things which have to be considered by industries to provide a safe and cost affective medicine to the patients like Supply chain, Waste management, Product management, Post- marketing surveillance, Good manufacturing practices and Marketing.
The U.S. pharmaceutical market is the world’s most important national market. Together with Canada and Mexico, it represents the largest continental Pharma market worldwide. The United States alone holds some 40 percent of the global pharmaceutical market. In 2014, this share was valued around 365 million U.S. dollars. Many of the global top companies are located in the United States. In 2014, six out of the top eleven companies were U.S.-based.
Track 6: Analytical Methodology
Analytical method development is the process of choosing an accurate assay procedure to determine the composition of a formulation. It is the process of proving that an analytical method is acceptable for use in laboratory to measure the concentration of subsequent samples Analytical methods should be recycled within GMP and GLP environments and must be developed using the protocols and acceptance conditions set out in the ICH guidelines. Analytical method development and validation stand the continuous and inter-dependent task associated with the research and development, quality control and quality assurance departments. Analytical procedures play a critical role in equivalence and risk assessment, management. It supports in formation of product-specific acceptance criteria and stability of results. Validation should establish that the analytical procedure is suitable for its intented purpose. Design of experiment is a powerful tool for the method characterization and validation.
Track 7: Nano Medicine & Nano Technology
Nano medicine is the medical application of nanotechnology. Nano medicine ranges from the medical applications of nanomaterial’s and biological devices, to Nano electronic biosensors, and even possible future applications of molecular nanotechnology such as biological machines. Current problems for Nano medicine involve understanding the issues related to toxicity and environmental impact of Nano scale materials (materials whose structure is on the scale of nanometers, i.e. billionths of a meter). Functionalities can be added to nanomaterial by interfacing them with biological molecules or structures. The size of nanomaterial’ is similar to that of most biological molecules and structures; therefore, nanomaterial’s can be useful for both in vivo and in vitro biomedical research and applications. Thus far, the integration of nanomaterial with biology has led to the development of diagnostic devices, contrast agents, analytical tools, physical therapy applications, and drug delivery vehicles.
Track 8: Analytical Chemistry and Engineering
Analytical chemistry, as the component of chemistry most diligently related to engineering, most involved in the development of new instrumentation and new technology, and most concerned with the applied applications of chemistry, has seen increased attention with the emergence of the mega-interdisciplinary parts of nanotechnology and systems biology.
Chromatography and mass qualitative analysis is employed for analysis of organic compounds. Electro spray ionization (ESI) could be a method employed in mass spectroscopic analysis. As relate to chromatography and mass spectrometry .HPLC is further flexible informative and trusted by the industry people. Recent advances in sample preparation techniques to beat difficulties encountered throughout measuring of little molecules from bio fluids mistreatment LC-MS. For Measuring, observation and protective your important Investments analytical chemistry instruments are used. Global Bioanalysis seminars are conducted and those specifically applied for chromatography assays, ligand binding assays to know more advances.
Analytical chemistry is that the study of the separation, identification, quality control and quality assurance of the chemical parts of natural and artificial materials .The maintenance of a desired level of quality in an exceptionally package or product, particularly by resources that of attention to every one stage of the method of delivery or production. Bioanalytical Chemistry could be a sub-division of bioanalytical chemistry that refuges the measuring of medicine, Ion sensors, Proteins and DNA Sequences in unnatural samples or concentrations. Accurate quantification of the drug samples is extremely very important for several scientific endeavours which can not delay the result. Therefore the Bioanalytical Techniques are in the main focussed to bring the correct results of the drug sample to supply an ideal result.
Track 11: New Instrumentation and Equipment
NMR analysis is recycled in separation of complex l and natural samples. Recent advances in mass chemical analysis part unit facultative improved analysis of endogenous metabolites. Here we have a tendency to deliberate many problems relevant to developing High-Performance Liquid Chromatography, electro spray ionization, mass chemical analysis conducts for targeted metabolomics (i.e., menstruation of dozens to many specific metabolites).Lab-on-a-chip devices range unit a set of MEMS instruments and infrequently indicated by "Micro Total Analysis Systems" (µTAS) still.
Bioanalysis may be a sub-discipline of analytical chemistry covering the quantitative action of xenobiotics (drugs and their metabolites, and biological molecules in unnatural locations or concentrations) and biotic (macro and micro molecules, proteins, DNA, giant molecule medicine, metabolites) in biological structures. Applications for analytical and Bioanalytical method development and validation, are as follows: biological safety test, clinical support, separation of mixture of compound, drug analysis. Prominence of understanding proteomics and process of food science is essential, and can be discussed by using separation techniques.
Track 13: Bio analytical Methodology
Bioanalytical Chemistry may be a sub-division of Analytical Chemistry that covers the measuring of medicine, Proteins and deoxy ribonucleic acid in unnatural samples or concentrations. In the Previous times, Bio analysis was supposed to be used for the measuring of little drug molecules, How ever since the explosion of biopharmaceuticals has started. Bioanalytical Techniques and validation are utilized in the measuring and analysis of huge molecule medicine. Bio analytical Chemistry improvement mostly started by the usage of the recently developed understated strategies that include: combined techniques like Chromatography, LC-MS, Spectroscopy and ultrafast spectroscopy, GC-MS and natural process strategies like HPLC.
In bioscience and drugs, to a small grade molecule may be a coffee mass (<900 Daltons ) compound which is incapable to facilitate regulate a process, with a size on the order of 10−9 m. Most drug analysis square measure identical little molecules. For analysis of small organic molecules the subsequent devices ought to be recycled are as follows HPLC method, chromatography, Ultraviolet-visible (UV-VIS) spectrophotometry, Infrared (IR) spectrometry and mass spectrometry.
Analytical techniques transform researchers to look at complicated relationships between variables and those methods are Regression Analysis, Grouping ways, Multiple Equation Models. Chemistry that involves the study of the molecular mechanisms fundamental the performance of the system, particularly the character of antibodies, antigens and their interactions. The foremost common diagnostic ways include: diagnostic assay, Endoscopy, Diagnostic Imaging, Blood Tests, immunochemical assay. The tremendous molecule detected by the bioassay is usually remarked as Associate in Nursing "analyte" and is in several cases a macromolecule. Analytes in biological liquids identical body fluid or area unit often measured abuse immuno assays for medical and analysis functions.
Track 16: Environmental Analytical Aspects
Environmental analytical chemistry is the scientific study of the chemical and organic chemistry phenomena that occur in natural places. Environmental chemistry is that the scientific study of the chemical and chemical science phenomena that occur in natural places. Quantitative & qualitative analysis may be a key a part of environmental chemistry, since it provides the information that frame most environmental studies or environment pollution studies. Common analytical techniques used for quantitative determinations in environmental chemistry embody classical wet chemistry, like menstruation, titrimetric and chemistry strategies. Sometimes due to climate changes in the atmosphere pests attaches the crops. To avoid loss of fertility and food safety in crops pesticides are used.
Track 17: Regulatory Affairs
Regulatory affairs (RA), is also called government affairs, is a profession within regulated industries, such as pharmaceuticals, medical devices, energy, banking, telecom etc. Regulatory affairs also has a very specific meaning within the healthcare industries (pharmaceuticals, medical devices, biologics and functional foods)
Regulatory affairs (medical affairs) professionals (aka regulatory professionals) usually have responsibility for the following general areas: Ensuring that their companies comply with all of the regulations and laws pertaining to their business, Working with federal, state and local regulatory agencies and personnel on specific issues affecting their business. i.e. working with such agencies as the Food and Drug Administration or European Medicines Agency (pharmaceuticals and medical devices); The Department of Energy; or the Securities and Exchange Commission (banking), Advising their companies on the regulatory aspects and climate that would affect proposed activities. i.e. describing the "regulatory climate" around issues such as the promotion of prescription drugs and Sarbanes-Oxley compliance.
Relevant Conferences: Drug Formulation Conference | Pharma Meeting | Pharma Events | Drug Research Events | Pharma Conferences
- 9th World Congress on Bioavailability & Bioequivalence April 16-18, 2018 Dubai,UAE
- 5th International Conference on Pain Medicine and Pain Management May 21-22, 2018 | New York, USA
- International Conference on Pharmaceutical Research and Development June 06-07, 2018 Philadelphia, Pennsylvania, USA
- 7th International conference on Pharmaceutical Auditing June 08-09, 2018 Philadelphia, Pennsylvania, USA
- 8th International Conference and Exhibition on Pharmaceutical Regulatory Affairs and IPR June 08-09, 2018 Philadelphia, Pennsylvania, USA
- 4th International Conference on Drug Discovery, Designing and Development June 27-28, 2018 Vancouver, British Columbia, Canada
- International Conference And Exhibition on Drug Safety & Pharmacovigilance August 29-30, 2018 Toronto, Canada
- 3rd International Conference on Generics Drugs and Biosimilars November 15-17, 2018 | Frankfurt, Germany
- 13th International Conference on Biologics and Biosimilars October 24-25, 2018 Boston, USA
- 12th Edition of International Conference on Nanopharmaceutics and Advanced Drug Delivery August 16-17, 2018 ,Dublin, Ireland
- 17th Edition of International Conference and Exhibition on Pharmaceutics & Novel Drug Delivery Systems October 04-06, 2018 ,Moscow, Russia
- 5th NovAliX Conference Biophysics in Drug Discovery June 13-15, 2018, Boston, USA
- 5th Annual Drug Discovery USA Congress 2 - 3 October 2018, San Diego, USA
- 21st Century Drug Discovery and Development for Global Health (S3) October 17—20, 2018 Hotel Palace Berlin, Berlin, Germany
Drug Information Association| Canadian Society for Pharmaceutical Sciences (CSPS)| Chemical Society Reviews| American Association of Pharmaceutical Scientists (AAPS)| Indonesian pharmaceutical association| Pharmaceutical Association of Malaysia (PhAMA)| Malaysian Pharmaceutical Society,| International Society for Biological Therapy of Cancer| Pharmaceutical Group of the European Union (PGEU)| The Pharmaceutical and Novel Drug Delivery Healthcare Sciences Society (PHSS)| Association of the British Pharmaceutical Industry (ABPI) | American Association of Pharmacy Technicians (AAPT)| American Associations of pharmaceutical scientists (AAPS)| The Pharmaceutical Research & Manufacturers Association (PhRMA)| Pharmaceutical Group of European Union (PGEU)|
Related Associations and Societies:
Societies in USA
Drug Information Association| Canadian Society for Pharmaceutical Sciences (CSPS)| Chemical Society Reviews| American Association of Pharmaceutical Scientists (AAPS)| American Association of Pharmacy Technicians (AAPT)| American Associations of pharmaceutical scientists (AAPS)| The Pharmaceutical Research & Manufacturers Association (PhRMA)
Societies in Asia and Pacific
Societies in Europe
Pharmaceutical Group of the European Union (PGEU)| The Pharmaceutical and Novel Drug Delivery Healthcare Sciences Society (PHSS)| Association of the British Pharmaceutical Industry (ABPI)| Pharmaceutical Group of European Union (PGEU)| Pharmaceutical Group of European Union (PGEU)
ConferenceSeries Ltd invites all the participants across the globe to attend 10th Annual Congress on Drug Design & Anlytical Techniques during September 03-04 , 2018 in UAE, Dubai which includes prompt keynote presentations, Oral talks, Poster presentations and Exhibitions. Drug Formulation 2018 is a specially designed cluster Pharmaceutical and Medicinal Chemistry Conference. The main theme of this Pharma conferences is “Recent innovations and approaches in Drug Formulation & Analytical techniques” 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 Pharmaceutical Sciences and Medicinal Chemistry, this is your single best opportunity to reach the largest assemblage of participants from the Pharma and medicinal community, Find out how innovators are closing the gap between product development and adoption, Better identify cyber threats and reduce information security risks, Debate the potential to greater cross-industry and cross-sector collaboration in the race for faster, cheaper, better cures. Conduct demonstrations, distribute information, meet with current and potential Scientists, make a splash with a new research, and receive name recognition at this 2-day event Pharmaceutical Science & Medicinal Chemistry. 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:
- 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 Entrepreneur
- Government healthcare departments, HTA’s and drug regulators
- Digital health companies
- Genomics and personalised medicine experts
The Global Drug Formulation Technologies Market is poised to grow at a CAGR of around 12.2% over the next decade to reach approximately $160 billion by 2025. Some of the prominent trends that the market is witnessing include growing identification of combinatorial chemistry technology, regulatory initiatives fostering demand for pharmacogenomics technology, proteomics in anticancer drug discovery and human protein microarray for various protein analysis.
This industry report analyzes the market estimates and forecasts for all the given segments on global as well as regional levels presented in the research scope.
The study focuses on market trends, leading players, supply chain trends, technological innovations, key developments, and future strategies.
With comprehensive market assessment across the major geographies such as North America, Europe, Asia Pacific, Middle East, Latin America and Rest of the world the report is a valuable asset for the existing players, new entrants and the future investors.
The Asia Pacific drug Formulation market in 2016 was worth $6224 million. The market is expected to reach $13462 million by 2024 at a CAGR of 10.1% between 2016 and 2024. Aging population, rise in healthcare spending and increase in lifestyle oriented diseases and fatalities are some of the factors driving the drug discovery market in the Asia pacific region.
The drug Formulation market by technology is segmented into QPCR, DNA Microarrays, Protein Microarrays, High–throughput screening, mass spectrometer, GEL Electrophoresis, Chromatograph, Protein and Nucleic Acid Isolation and other technologies.
The countries analyzed in the Asia Pacific drug Formulation market are India, China, Japan, Korea, Australia and rest of Asia Pacific. The entry of new companies in the market and substitute products acts as a threat to the Asia pacific drug discovery market. Discovery of new drugs being delayed due to government regulations is a big restraint. Also, the drug market is shifting from branded to generics drugs which limit the growth of the drug discovery market in this region.
Pharmaceutical Associations: https://drugformulation-bioavailability.pharmaceuticalconferences.com/
American Association of Pharmaceutical Scientists (AAPS)
US Food and Drug Administration (FDA)
American Society for Clinical Laboratory Science (ASCLS)
National Cancer Institute Center for Cancer Research (NCI)
American Association for Clinical Chemistry (AACC)
American Society for Pharmacology and Experimental Therapeutics (ASPET)
Association of Clinical Research Organizations (ACRO)
International Pharmaceutical Manufacturers Group (IPMG)
Past Conference Report
Drug Formulation 2017
Drug Formulation 2017 Report
Conference Series LLC hosted the Drug Design & Drug Formulation at Courtyard Seoul Times Square, Seoul, South Korea during October 19-20, 2017. The conference was designed around the theme of “Advanced Drug Formulation perspectives for Comprehensive Bioavailability” and was a great success where eminent keynote speakers from various reputed companies made their resplendent presence and addressed the gathering. Moreover, the networking sessions laid the foundation for some time worthy collaborations between many start-up and big industries. The post conference networking lunch session witnessed a number of B2B meetings that are turning up to be mutually beneficial to both the organizations who had gone in for the business meetings.
Drug Formulation 2017 witnessed an amalgamation of peerless speakers who enlightened the crowd with their knowledge and confabulated on various new-fangled topics related to the field of pharma. This congress not only brought forward the latest developments in the field but also provided solutions to the numerous challenges encountered in developing a drug.
Conference Series LLC would like to convey a warm gratitude to all the Honourable guests, Keynote Speakers, Delegates, Media Partners and Exhibitors for their participation in Drug Formulation 2016.
We on behalf of the conference specially thank the exhibitors for their participation in the congress and also the media partners for their wonderful marketing of the event. Conference Series LLC also took the privilege of felicitating Drug Formulation 2017 Organizing Committee, Keynote Speakers, and Chair whose support made conference a great success.
With the enormous feedback from the participants and supporters of Drug Formulation 2017, we are glad to announce “10nd Annual Congress on Drug Formulation and Analytical Techniques” during. July 16-17, 2018 Melbourne, Australia
For more details visit: http://drugformulation-bioavailability.pharmaceuticalconferences.com/
Past Reports Proceedings Gallery
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