Intellectual Property Rights
That any pharma product has successfully pass through the . Biosimilars and biologics are no exceptions. The companies developing these biosimilars and biologics apart from regulatory aspects tend to enjoy monopoly over their product. <span style=""font-size:" 10.5pt;="" font-family:="" helvetica,="" sans-serif;="" color:="" rgb(51,="" 122,="" 183);="" text-decoration-line:="" none;"="">Intellectual 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. In this year 16 IPR petition was filed. So, expected scenario of 2017 would be a boom in Biosimilar and biologics field.
- Pharma patent scenario
- Criteria for patentability and patent claims
- Critical research issues
- Recent patent disputes and litigations
- Evaluation of highly variable drugs and drug products
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Intellectual Property Rights Conference Speakers
Recommended Sessions
- Analytical Strategies of Biosimilar
- BCS and IVIVC Based on Biosimilars
- Bioequivalence assessment
- Biological Medicine
- Biosimilars Research Pipeline
- Brexit Effect on Biosimilar
- Clinical Development of Biosimilars
- Current Agency Expectations for Approval for Biosimilars
- Current Challenges in Developing Biosimilars
- Drug Delivery and Development
- Emerging Biosimilars In Therapeutics
- Globalization of Bio Similar
- Intellectual Property Rights
- Pharmacovigilance challenges in Biosimilars
- Regulatory Approaches of Biosimilars
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