Clinical Trials of Biosimilars
As the demand of Biosimilars is ever increasing in the pharmaceutical market, it is very important to check them properly before releasing it to the mass. That is why there is a stepwise approach towards clinical trials of Biosimilars. It has various levels such as Extensive Molecular characterization Program, Pre-Clinical, Phase 1, Phase 3, Phase 4 and so on.
- Biosimilars Clinical Studies
- Biosimilars Toxicological studies
- Targeted cell line development
- Transgenic animals
- Case studies and clinical models
- Risk management and quality affairs
- Clinical trials on major diseases
Related Conference of Clinical Trials of Biosimilars
April 07-08, 2025
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&
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Clinical Trials of Biosimilars Conference Speakers
Recommended Sessions
- BCS and IVIVC Based Biowaivers
- Bioequivalence Assessment
- Biopharmaceuticals
- Biosimilars Development
- Biosimilars in Oncology
- Biosimilars in Therapeutics
- Biosimilars Pipeline
- Challenges in Pharmacovigilance
- Clinical Trials of Biosimilars
- Drug Development and Delivery
- Globalization of Biosimilars
- Intellectual Property Rights
- Legal Issues and BPCI Acts
- Regulatory Approach for Biosimilars
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- The Future of Pharma R&D - Future Pharma 2025 (Netherlands)
- The Next Generation Approach of Antibiotics - Antibiotics Resistance 2025 (Canada)
- Toxicology - Pharmacology 2025 (France)
- Translational Research - Personalizedmedicine-2025 (Switzerland)
- Types of Formulations - Formulations 2025 (France)
- USFDA Approved Biosimilars - Eurobiosimilars 2025 (France)
- Vaccine Delivery Systems - Pharmaceutica-2025 (Canada)
- Vaccine Design and Drug Design - PHARMA CONFERENCE-2025 (France)
- Vaccine Drug Delivery Systems - PHARMACEUTICA 2025 (Germany)
- Vascular Pharmacology: Focus on Endothelial Dysfunction - Cardiovascular-2025 (France)
- Wearable Drug Delivery Systems - PHARMA CONFERENCE-2025 (France)