Developing Biosimilars & Biobetters
Biosimilars are surmounting pharmaceutical business division from most recent three decades and deals appear to extend coherently. Advances in the biotechnology prompt to change and exposure of new natural items (Biosimilars) to treat diverse life-debilitating illnesses. Biosimilars are organic medications that are conveyed after expiry of the patent of affirmed pioneer and include Hatch-Waxman act is the amendment to Federal, Food, Drug and Cosmetics act which established the modern system of approval of generics through Abbreviated New Drug Applications (ANDAs).
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Developing Biosimilars & Biobetters Conference Speakers
Recommended Sessions
- Bioequivalence Assessment
- Biological Medicines
- Biological Medicines
- Biosimilars Approval to Biogenerics in Clinical Practice
- Biosimilars Market Strategy
- Challenges in Biosimilars
- Chemical and Analytical Strategies for Biosimilars
- Consequences of Brexit on Biosimilars
- Current Agency Expectations for Approval for Biosimilars
- Developing Biosimilars & Biobetters
- Emerging Biosimilars in Therapeutics
- Innovative Approaches for Biosimilars
- Intellectual Property Rights
- Legal Issues and BPCI Act
- Novel Drug Delivery Technologies
- Regulatory Advances in Biosimilars
- USFDA Approved Biosimilars
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