Generic Drugs 2021
We welcome all the participants from all over the world to attend Global summit on Generic Drugs and Quality Control, this auspicious event is to be hosted as Webinar in 2021. We cordially welcome all the international participants, eminent researchers, students, business entrepreneurs and delegates.
Generic Drugs 2021 is a unique opportunity to discuss best practices within the laboratory and those in Pharmacy industries, There will be many seminars and technical sessions taking place which will catch the attention of the professionals to attend Generic Drugs 2021 Webinar and, here we can get a chance to know views of different people working in Pharmaceuticals and related subject which can help us improve our own ideas and processes. Generic Drugs 2021 summit is designed to cover various aspects field of which include pharmaceutical analysis, Biosimilars, Generic trends, Good Manufacturing Practices (GMP), Complex Generic Drugs, Animal Generic Drugs.
Generic Drugs 2021 is aimed to promote innovation, to share advanced knowledge about Quality Control and to encourage applications of Good Manufacturing Practices.
With members from around the world focused on learning about Generic Drugs and Quality Control; this is your best opportunity to reach the largest assemblage of participants from the Generic Drugs Community. Conduct presentations, distribute information, meet with current and potential scientists, make a splash with new Techniques in Generic Drugs and Quality Control, and receive name recognition at this 2-day online event.
Track 1: Best Practices & Strategies for Generic Drug Development
Spurring innovation is required for development in generics field, advanced scientific methods, quality data and the use of sophisticated quantitative methods and computational methods are to be implemented, A specific category of drugs that are at times been difficult to make equivalent generics(complex generics) represent some very expensive drugs and are widely used generics, the products with complex active ingredients such as peptides, polymeric compounds, complex mixtures of Active pharmaceutical ingredients(API) Complex formulations such as liposomes, colloids etc. Drugs with complex route of delivery such as topical drugs and ophthalmological products that are often formulated as suspensions.
Track 2:Modernization of Bioequivalence Standards for Generic Products
Bioequivalence (BE)/bioavailability(BA) contemplates assume a significant part in drug improvement both for new medication and their conventional reciprocals, these investigations are additionally done before the endorsement of medication (post endorsement period) and are communicated in fundamental openness measures, like Area under plasma Concentration-Time curve(AUC) and greatest focus C-max these actions are accepted to relate with security and viability out comes that may communicated by biomarkers. This (BA), (BE) contemplates give significant data in generally set of information that guarantees the security and adequacy to the experts and patients.
Track 3: Application of Quantitative systems pharmacology (QSP)
QSP is a quantitative stage that covers a wide range of devices, of which physiologically based models and quantitative clinical pharmacology (QCP) depicts drug testimony and related changeability in individuals. In nonexclusive medications, QP approaches coordinate natural, physiological and drug properties to set up clinically pertinent bioequivalence (BE). QCP approaches are fundamental to assess plan and affectability to lessen cost and season of complex medication improvement.
Track 4: Bioequivalence approaches for complex injectable API and formulations
Track 5: Generic Animal Drug
In the veterinary drug market, the ascent in the conventional medications for creature medical services is the most recent pattern, the monetary advantage of nonexclusive medications is empowering the pet sweethearts to deal with their pets more efficiently.in the new years FDA is endorsing the many number of nonexclusive medications for the felines and canines which has prompted the reception of conventional medications by the veterinarians, it is assessed that about 80% of the veterinarians are recommending the nonexclusive medications to set aside the pet proprietors cash. In any case, the lower edge of benefit given by the conventional medications contrasted with the marked medications should be glanced in by the veterinary experts
Track 6: Pharmaceutical Quality Assurance
The motivation behind Quality Assurance is to guarantee that medication arriving at each customer or patient is protected, viable, and fulfills quality guidelines. A far reaching quality confirmation program incorporates both specialized and administrative exercises, numerous zones inside a medical care framework are associated with quality affirmation, including acquisition, drug store, clinical, nursing divisions, just as medication therapeutics board by acquiring quality items which are protected and successful through organized choice and obtainment techniques, keeping up nature of items through the proper stockpiling, checking and conveyance and recommending strategies.
Track 7: Challenges of Manufacturing Generic Drugs
Track 8: Acceptance of Generic Drugs by People
Worldwide medical care use is developing consistently and utilization of conventional medication is supported as cost cutting measure by numerous nations and their legislatures, as nonexclusive prescriptions are by and large low costly than their exclusive partners because of numerous reasons which incorporate skipping need to innovative work cost, less market rivalry.
Track 9: Challenges of Marketing Generic Drugs
Albeit the quicker endorsements of nonexclusive item incouraging, there are as yet numerous difficulties to bring new monetary and reasonable item into the market that empowers makes to make a few benefits and stay above water as the expense of making conventional medications is same as marked medications, yet marked medications appreciate the more noteworthy benefits on account of patent insurance.
Track 10: Biosimilars
A biosimilar is a biologic clinical item that is an indistinguishable duplicate of a unique item. Biosimilars are basically indistinguishable from authorized unique reference item with minor contrasts in clinically idle parts; likewise, there are no clinically significant contrasts between the natural and the reference item regarding wellbeing, immaculateness, and power. Albeit both nonexclusive medications and biosimilars have related business premise, they are two totally various items with regards to their construction, advancement and approval. Biosimilars are turning into an inexorably huge in the field of drugs industry around the world, the difficulties to create and show biosimilars ought to beat the characteristic contrasts in the bioprocess fabricating and organic, physiochemical portrayal of a biosimilar contrasted and a few diverse reference items. The mechanical troubles to make duplicate of items while focusing on administrative and market requests is needed to help advancement toward accomplishing profitable assembling measure
Generic Drug Market by Brand (Branded Generic and Pure Generic) for Central Nervous System (CNS), Dermatology, Respiratory, Cardiovascular, Oncology, and Other Therapeutic Applications - Global Industry Perspective, According to the market analysis report, the International Generic Drug market estimated to be across 200.20 Billion USD in 2015 and is expected to reach approximately USD 380.60 billion by 2021, growing at a CAGR of about 10.8 % from 2016 and 2021.
It is driven by the factors such as cost-effectiveness and135 billion worth patented drugs expiry and Government initiatives has given it a competitive lead over the branded drugs in the market, Nearly $150 Billion USD worth drug patents are about to expire in 2020 which can drive Generic drug market into profits.
North America is beholder of the largest share in the generic drug market, In US 89% of the prescribed drugs are Generic and the demand is high for generic drugs, In the Asia pacific region India and China dominated the Generic drug market in volume, total Indian generic drugs market was around 21billion USD in the year 2015 mainly due the Indian companies getting international regulatory approvals like U.S FDA, MHRA.UK, TGA Australia and MCC South Africa. Brazil was the largest Generic market in Latin America it is due to the sale of Generic medicine was accounted for 23% and will remain to be dominant in forecast period due to high demand and increasing development in the pharma sector. Europe is observed to show significant growth in Generic drug market as result of prevalence of chronic diseases and government support.
- Best Practices & Strategies for Generic Drug Development
- Modernization of Bioequivalence Standards for Generic Products
- Application of Quantitative systems pharmacology (QSP)
- Bioequivalence approaches for complex injectable API and formulations
- Generic Animal Drug
- Pharmaceutical Quality Assurance
- Challenges of Manufacturing Generic Drugs
- Acceptance of Generic Drugs by People
- Challenges of Marketing Generic Drugs
- Current Good manufacturing practices (CGMP)
- Quality by Design (QbD) for generic drugs
- Super Generic drugs and Bio Betters
- Patent Access& Intellectual property& FDA Regulations
- Complex Generic Drug Product
To share your views and research, please click here to register for the Conference.
All accepted abstracts will be published in respective Our International Journals.
Abstracts will be provided with Digital Object Identifier by