World Congress on Biologics and Biosimilars
Biologics meet 2021 invites all participants from around the world to participate in the "World Congress on Biologics and Biosimilars” to be held on November 16-17, 2021 Webinar, and will cover all aspects of the pharmaceutical sciences, manufacturing, quality with a strong emphasis on originality and scientific quality.
World Congress on Biologics and Biosimilars
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World Congress on Biologics and Biosimilars
Theme: “Advanced Research and Emerging Issues in the Field of Biologics and Biosimilars during COVID-19â€.
Renowned Speakers
Tatsuya TakagiOsaka University Japan
Japan
Alexei BasnakianDNA Damage and Toxicology Core Center University of Arkansas USA
USA
Mitsuji YamashitaShizuoka University Japan
Japan
Margitta DatheLeibniz-Forschungsinstitut für Molekulare Pharmakologie Germany
Germany
Ilayda Acaroglu DegitzYeditepe University Turkey
Turkey
Felix-Martin WernerEuro Academy Pößneck Germany
Germany
Janina-Miriam NoyThe University of New South Wales Australia
Australia
Matthew N BahrGlaxo Smith Kline USA
USA
Biologics Meet 2021
Biologics meet 2021 invites all participants from around the world to participate in the "World Congress on Biologics and Biosimilars” to be held on November 16-17, 2021 Webinar, and the theme of Biological Meet 2021 is “Advanced Research and Emerging Issues in the Field of Biologics and Biosimilars during COVID-19” will cover all aspects of the pharmaceutical sciences, manufacturing, quality with a strong emphasis on originality and scientific quality.
Conference Series LLC LTD organizes 1000+ Conferences every year across USA, Europe & Asia with support from 1000 more scientific societies and publishes 1000+ Open access journals which contain over 70000 eminent personalities, reputed scientists as editorial board members, 1200 Symposium & Workshops and 5 million followers. Conference Series Ltd invites all the participants across the globe to attend the “World Congress on Biologics and Biosimilars "
Biologics meet 2021 describes recent developments in the marketing and production of pharmaceutical drugs and contract manufacturing. A comprehensive knowledge of a scientific discipline that describes the effects of Biosimilars drug marketing and Biologics meet 2021 is now exploring the scope of Biosimilars drug marketing in the industry. Biologics meet 2021 provides detailed market, technology, and industry analysis to help readers quantify and qualify the generic prescription market. Significant trends are identified and sales forecasts by product category and major national markets are based on industry sources and an assessment of the regulatory environment, health policies, demographics and other factors directly affecting the generic market. The wider economic environment is also considered.
Why attend Biologics meet 2021:
Keynote presentation along with interactions to galvanize the scientific community.
Workshop and symposiums to reach the largest assemblage of participants from the Pharma/Biotech community.
A wide track of exhibitors to showcase the new and emerging technologies.
Platform to global investment community to connect with stakeholders in Pharma/Biotech sector.
Young Scientist/ Investigators Award geared towards best budding young research
Links to the political marketing resources to expand your business and research network.
Triumph of Awards, Certificates recognizes your commitment to your profession to encourage the nascent research.
Target Audience:
Directors, CEOs of Organizations
Business Development Manager
Chief Scientific Officers
R&D Researchers from Biosimilar and Biologics Industries
Professors, Associate Professors, Assistant Professors
PhD Scholars
Patent Attorneys
Intellectual Property Attorneys
Investment Analysts
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 Entrepreneurs
Biologics meet 2021 has everything you need:
Open Panel Discussions: Provide an open forum with experts from academia and business to discuss current challenges in Biosimilars & Biologics, where all participants can interact with the panel, followed by a Q & A session.
Speaker and poster presentations: Provide a platform for all academics and industry professionals to share their thoughts and research findings through a speech or poster presentation.
Editorial Board Meeting: Discussion on the growth and development of open access journals in Bioanalysis and Biomedicine, as well as the recruitment of committee members and reviewers to support the journal.
Roundtables: Provide a platform where industry professionals meet with academic experts.
More than 50 international organizations and pavilions will exhibit at Biologics meet 2021 pharma conference. Exhibitors will include equipment manufacturers and suppliers, system suppliers, finance and investment companies, research and development companies, developers’ projects, trade associations and government agencies.
In addition to products and services, you will have access to valuable content, including keynote presentations, product demonstrations, and training sessions offered by industry leaders today.
The Biologics meet 2021 brings together everything you need, under one roof, to save you time and money. This is the event not to be missed!
A two-day rally that examines future market models, creative business methodologies and open doors to the development of moderate medicines. Pioneers in the pharmaceutical industry want substance and roundtable reviews to remain for systems administration and air. This meeting is officially the largest non-proprietary key meeting of the company and will provide members with a comprehensive overview of the business methodology for moderate medications.
Get your image before senior chiefs
Break into the lucrative Generic Medicines industry
Position your organization as an industry pioneer
Make deals leads and convey an arrival on venture
Connect with your objective market in the locale.
Pharma Biosimilars 2020
We gratefully thank all our wonderful Speakers, Conference Attendees, Students, Media Partners for making Pharma Biosimilars 2020 Conference the best ever and memorable!
The International Conference on Biosimilars & Pharmaceuticals, hosted by the Conferenceseries LLC was held during November 16-17, 2020 Kyoto - Japan based on the theme “Essential innovation in Pharma biosimilars’’. Benevolent response and active participation was received from the Organizing Committee Members along with Scientists, Researchers, Students and leaders from various fields of Pharmaceutical Science, who made this event a grand success.
The Conference focused on recent developments in the Pharmaceutical Science sector and the meeting engrossed in knowledgeable discussions on subjects like:
- Analytical Strategies of Biosimilar
- Emerging Biosimilars In Therapeutics
- Current Challenges in Developing Biosimilars
- Regulatory Approaches of Biosimilars
- Pharmacovigilance challenges in Biosimilars
- BCS and IVIVC Based on Biosimilars
- Globalization of Bio Similar
- Clinical Development of Biosimilars
- Bioequivalence assessment
- Biosimilars Research Pipeline
- Intellectual Property Rights
- Brexit Effect on Biosimilar
- Drug Delivery and Development
- Current Agency Expectations for Approval for Biosimilars
- Biological Medicine
The conference was initiated with the Honourable presence of the Keynote forum:
Session Chair: Lincy Joseph, Pushpagiri College of Pharmacy, India
Title: Challenges in developing biosimilars
Subir K Basak, International Finance Corporation, USA
Title: Water as an alternative medicine in cell biology
Insang Lee, Divine Lab Co Ltd, South Korea
Title: Risk base Technical transfer in pharmaceutical manufacturing
Kunihiko Furuzaw, GMP Consultant, Japan
Title: Pharmacological screening of oxazines for epilepsy
Mathew George, Pushpagiri College of Pharmacy, IndiaHouston, USA
Poster Presentation:
Title: Navigating the biosimilar journey from bench to market: A general overview and case studiesSuliman Al-Fayoumi, Al-Fayoumi Consulting, USA
Title: Anti-MRSA activity of cationic lipid carriers in combination with oxacillin for eradicating skin Infection
Jia-You Fang, Chang Gung University, Taiwan
Title: Screening of novel oxazepines for anticonvulsant effect
Lincy Joseph, Pushpagiri College of Pharmacy, India
Title: Antibacterial activity of collagen/gelatin/sodium alginate biomaterial with liposomes
immobilized releasing antibiotics
Ming-Cheng Chang, Institute of Nuclear Energy Research, Taiwan
Video Presentation:
Title: Design of bioavailability and bioequivalence studies through PK-Stat approach
Jaganmohan Somagoni, ClinSync Clinical Research Private Limited, India.
Conferenceseries LLC offers its heartfelt appreciation to organizations such as Go EVNTS & Bentham Science and other eminent personalities who supported the conference by promoting in various modes online and offline which helped the conference reach every nook and corner of the globe. Conferenceseries LLC also took privilege to felicitate the Keynote Speakers, Organizing Committee Members and Chairs who supported this event.
With the grand success of Pharma Biosimilars 2021, Conferenceseries LLC is proud to announce the "World Congress on Biologics and Biosimilars" to be held during November 16-17, 2021 is Webinar based on the Theme: Organic products meet: current scenario and future prospects Pharmaceutical Sciences.
Sessions/Tracks
Track 1: Analytical Strategies of Biosimilar
Biologics and Biosimilar analysis make the one among the foremost important aspect on the event on biological products. the utilization of production technologies like disposable and provide chain logistics can help companies such establish flexibility facility involved in biosimilar analytical methods.
Bio analytical methods include altogether global events of biosimilars for example: GMP protein analysis, pre-clinical and clinical program, Bioassay for comparability and potency testing.
Track 2: Emerging Biosimilars in Therapeutics
In the field of biologics, the new avenue has created towards clinicians because explorations have created for better disease management. within the treatment of ailments like psoriasis, rheumatic arthritis, certain cancer inflammation, bowel diseases etc. showed some good outcomes due to using biologics. Biosimilar insulins which are newly formed are likely to enter the insulin landscape as patents for major branded insulin products able to expire within the next few years. The emerging biosimilar like filgrastim, peg filgrastim, recombinant blood products, therapeutic products vaccine biosimilar, anti-bodies growth hormones, biosimilar peptide, of these are wont to sound knowledge on biosimilars development on drugs.
Track 3: Current Challenges in Developing Biosimilars
For the event of biological calls many changes may occur. Concepts of biologics with considerations at initial stages, clinical developments are essential at early. For the successful development of biologics follow on proper scientific and strategic approaches are need. most likely , the drug safety factors and labelling requirements are the overcoming challenges and important in continue lately clinical steps. And now it's much required to develop a drug product in consistent with quality intentionally .
Track 4: Regulatory Approaches of Biosimilars
biosimilars is likewise called as nonspecific adaptation of biosimilars. The clinically idle compound isn't withstanding with biosimilars but rather minor contrasts and profoundly like authorized item; additionally, there Presently a-days in pharmaceutical industry biosimilars is formed has another buzz. Furthermore, these are not any clinically important contrasts between the biologicals and therefore the reference item as far as intensity, wellbeing and immaculateness. The worldview of customary generics to biosimilars, and different parts of Biosimilar endorsements. Also, these Biosimilars 2019 will provides a phenomenal and overall chance to the researchers, accomplices and pharma pioneers from Biopharmaceutical and Biotechnology businesses to enhance and to research the key marketplace for Biosimilars and Biologics with an unmistakable photo of the executive approach for biosimilars and biologics. The US biosimilars, European biosimilars, Canada biosimilars, UK biosimilars take an interesting part in cross the world by 2019. Biosimilars development. And these biosimilar conferences will mainly specialise in bio similar development to deliver safe and successfully.
Track 5: Pharmacovigilance challenges in Biosimilars
Same proportion pharmacovigilance for biosimilars has comparatively more different from other products. Biosimilars 2019 session mainly look that have already been announced to incorporate enhanced tracking and follow-up of post marketing surveillance issues, and on FDA initiative planned different changes in AERS, pilots of latest developed post market strategies of drug-monitoring and ADR related problems. the rules of biosimilars for pharmacovigilance and pharma epidemiology are the points that shall be laid emphasis within the session In USA average annual income mostly spend on biologics comparing to generic drugs for example:16% on biologics and three on other drugs.
Track 6: BCS and IVIVC supported Biosimilars
These Mainly discusses about differing types of medicine and adsorption distribution metabolism excretion pathways. And This biosimilars includes, In vitro diffusion cells for dissolution testing in formulation development, The preclinical testing of ADME in INVITRO. the first moto of this work was to suggest the biosimilars potential of biopharmaceutical arrangement which are known to extend the dissolution. These insoluble drugs which is orally absorbed. These Aims at addressing all such challenges of the pharma formulation sector at biologics and biosimilars at 2019 conference. The solubility includes in biopharmaceutical classification.
Track 7: Globalization of Bio Similar
These tracks mainly affect biosimilar meetings those that can attend by following biologics/protein/biosimilar product process science, New biosimilar development, portfolio Management, Reasearch&development, biosimilar market, business operations, scientific affairs. This track mainly discusses about Risk-sharing arrangement LATAM marketplace for bio-similar adopting innovative mechanism for generic drugs impact on global bio similar market and price and risk management.
Track 8: Clinical Development of Biosimilars
Risk Management, quality affairs, Case studies, clinical models, Transgenic animals Targeted cell-line development, clinical biosimilar tracks are major diseases of clinical trials. The pkd/docx studies toxicological studies and Aspects of genotoxicity tests. And These tracks are designed especially for those that are having more knowledge on clinical studies and clinicians’ prospects for biosimilars. These guidelines on the above-mentioned topics also are to be thrown effect upon at this biosimilars conference.
Track 9: Bioequivalence assessment
The active ingredient from the pharma product and its absorption into the circulation is especially specialise in equivalence release. Bioequivalence assessment includes strategies of topical dosage forms and bio equivalence approaches for transdermal dosage form and assessment of respiratory dosage form.
Track 10: Biosimilars Research Pipeline
The biological medical product may be a biosimilar manufactured by a special company by the copy of an ingenious product. the first biosimilar innovator products are officially approved biosimilar are often manufactured when the originally product patient expire. This session shall be highly useful for the biosimilar industry researchers to update themselves on the newest research updates from everywhere the planet . Not only these sessions and also there are some ways to seek out the precise place for all the biosimilar exhibitions related to present generation of biosimilars and biologics.
Track 11: property Rights
That any pharma product has successfully undergo the regulatory affairs scanners before launched within the market need less to say . Biosimilars and biologics are not any exceptions. the businesses developing these biosimilars and biologics aside from regulatory aspects tend to enjoy monopoly over their product. property Rights (IPR) and patents are ultimate tools to the biosimilar manufacturers for safeguarding their interests. 2016 was a record year for development of Biosimilars & biologics in US. during this year 16 IPR petition was filed. So, expected scenario of 2017 would be a boom in Biosimilar and biologics field.
Track 12: Brexit Effect on Biosimilar
The negative tendency of biosimilars Brexit impact. The hindrance towards the value cutting approach taken by the NHS may be a major setback towards approval and launch of biosimilars in market. With Britain being among foremost clinical preliminary focuses is claimed to ascertain a diminishing within the eagerness of the manufacturers and specialists to try to to any longer preliminaries in Britain. Additionally, Brexit will cause the first rationale of British Biosimilars Association (BBA) to fall back-which went for expanding the use of Biosimilars.
Track 13: Drug Delivery and Development
Medication Delivery Companies and Market session is beginning to change for small , large, and medium scale pharmaceutical, Co biopharmaceutical Manufacturing and Industries, bland medications organizations, contract sedate conveyance organizations which may show from improvement to assembling. Tending to those dangers is a unprecedented test, due to the many-sided quality of the Clinical bio therapeutics themselves.
Track 14: Current Agency Expectations for Approval for Biosimilars
Biosimilars are a generally new subset of biopharmaceuticals, with the biotechnology business eventually developing to such an extent that off-patent nonexclusive compose items progressively will enter real markets. Up so far , quite 20 biosimilars for a group number of reference items are affirmed in realhttps://biologicsmeet.pharmaceuticalconferences.com/abstract-submission.php markets, principally the ecu Union. Just two items are formally endorsed as biosimilars within the us . The parent field of biopharmaceuticals itself keeps on displaying a poor supporting framework of knowledge assets. Those biopharmaceutical and biosimilar data assets that do exist for the foremost part are restricted in number, assorted variety, and advancement.
Track 15: Biological Medicine:
Organic Medicine works with the science of the body and its regular recuperating capacities and additionally the otherworldly, passionate and physical parts of malady. Sickness implies that the body's direction isn't working legitimately and will be brought once more into its normal powerful state where the invulnerable framework is fully control. It during this manner searches for main drivers for the showing side effects of sickness the hidden elements making a person provides a specific disease. These underlying drivers may comprise of a couple of elements which have developed after a while and may incorporate; consume less calories, sustenance sensitivities, intestinal unsettling influences, case history , push, ecological elements, substantial metals, dental issues, hyperacidity, injury, introduction to microscopic organisms or infections or electromagnetic aggravation.
Market Analysis
The global biosimilars market should reach $60.1 billion by 2025 from $15.7 billion in 2020 at a compound annual growth rate (CAGR) of 30.9% for the forecast period of 2020 to 2025.
Companies Mentioned
· 3S Bio Inc.
· Alvotech
· Amgen Inc.
· Bio-Thera Solutions Ltd.
· Biocad
· Biocon Ltd.
· Bioeq Gmbh
· Biopartners Gmbh
· Biosidus S.A.
· Bioxpress Therapeutics S.A.
· Blau Farmaceutica S/A
· Boehringer Ingelheim Pharmaceuticals Inc.
· Celltrion Inc.
· Chong Kun Dang Pharmaceutical Corp.
· Cinnagen
· Cipla Ltd.
· Coherus Biosciences Inc.
· DM Bio Ltd.
· Dong-A Socio Holdings
· And Many More Companies!
Biosimilar drugs have gained immense popularity because of their impact on the lives of many patients. These drugs belong to several drug classes including hormones, interferons, growth factors (colony stimulating factors, erythropoietin) and monoclonal antibodies, among others. The use of these drugs has aided in the affordable treatment of many life-threatening diseases ranging from cancer and diabetes to chronic inflammatory diseases such as rheumatoid arthritis, psoriatic arthritis and others. The high cost of branded biologics has made biosimilars a lucrative alternative for affordable treatment. According to this report on biosimilars, the global market for biosimilars is expected to reach close to $20.8 billion by 2022, growing at a CAGR of 30.5%. Other drivers for this market include rising aging populations, patent expirations of many blockbuster drugs, and better healthcare provisions.
This updated report provides an in-depth analysis of the market for biosimilars in a global context, including market forecasts and sales through 2025. This study surveys the market for biosimilars in all the geographic regions including North America, Europe, the developed rest of the world (RoW), and emerging markets. The emerging markets include countries like India, China, Taiwan, Africa and Latin America.
The report provides an analysis of the market for biosimilars in various segments, for instance, by type, by region and by application/disease category. The report will include a detailed overview about the subject wherein the classification of biosimilar drugs along with their approval mechanisms, clinical trials and applications under review are elaborated upon.
The report also provides relevant patent analysis in both the U.S. and the European Union and comprehensive profiles of companies that lead the biosimilar drugs industry. The industry structure, focusing on the important biosimilar drug manufacturers/suppliers and their market shares and product offerings, is analyzed. This report also discusses the current market situation by elaborating upon the market drivers, restraints, challenges and opportunities. Separate chapters discuss the regulatory aspects and clinical trials. The latest news pieces including new products, new indications, mergers and acquisitions in the market are also dealt with in sufficient detail.
Excluded from this report are bio betters, generics of small molecule drugs and the bio generics pertaining to vaccines and blood products. The different requirements for approval and bioequivalence between generics and biosimilars put them in an entirely different regime.
The Report Includes
· 69 data tables and 73 additional tables
· An updated review and industry insights of the global biosimilars market
· Analyses of the global market trends, with data from 2018 to 2020, and projections of compound annual growth rates (CAGRs) through 2025
· Highlights of the emerging market regulations, clinical trials, and new products launches; and their impact on the stakeholders in this market
· Discussion of the biosimilars industry structure, opportunities and complexities, regulatory updates and penetration of biosimilar product classes in various regions worldwide
· Estimation of current market size and potential growth forecast for biosimilars market, and corresponding market share analysis by product type, application/disease category and geographic region
· A detailed review of patents issued for biosimilars by different assignee categories
· Impact analysis of COVID-19 pandemic on the growth of biosimilars market as compared to overall pharmaceuticals industry with respect to clinical trials/approval
Market Overview
The biosimilars market was valued at approximately USD 28,235 million in 2020, and it is expected to witness a revenue of USD 103,638 million in 2026, with a CAGR of 24.2% over the forecast period.
The impact of COVID-19 on the biosimilars market may be significant, and it has imposed a great challenge to the pharmaceutical companies focused on biosimilar development. The reduction in the FDA approval of non-COVID therapeutics during the current pandemic is expected to delay the process of product approvals and launches, thereby, hindering the market growth. Also, as most of the clinical trials have been postponed to combat the COVID-19 situation and minimize the infection among participants, most of the pipeline products are exhibiting a slow pace of research and development activities. Also, due to the lockdown and travel restrictions across the world, there is a shortage in supply chain and raw materials.
Those with submitted Abstracts will get an Acknowledgment mail enabling them to enrol for the gathering.
Abstracts will be compiled, and conference books are made available to participants at the conference.
Any presenter who is unable to attend should arrange for another qualified individual to present the paper/poster in question. If such a change is necessary, please notify our conference team
SUBMISSION OPTIONS:
Oral paper introductions will have 30-minute schedule time slot. The keynote session will have for 45-minute presentation duration, workshop/special session will have 1-hour long schedule opening and symposium will have 1-hour long availability followed by 5-minute Q&A session.
Graduate and master’s understudies are qualified to present their abstracts under poster and e-poster presentation category.
Conference Highlights
- Analytical Strategies of Biosimilar
- Emerging Biosimilars In Therapeutics
- Current Challenges in Developing Biosimilars
- Regulatory Approaches of Biosimilars
- Pharmacovigilance challenges in Biosimilars
- BCS and IVIVC supported Biosimilars
- Globalization of Bio Similar
- Clinical Development of Biosimilars
- Bioequivalence assessment
- Biosimilars Research Pipeline
- property Rights
- Brexit Effect on Biosimilar
- Drug Delivery and Development
- Current Agency Expectations for Approval for Biosimilars
- Biological Medicine:
To share your views and research, please click here to register for the Conference.
To Collaborate Scientific Professionals around the World
| Conference Date | November 16-17, 2021 | ||
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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