Patent Access& Intellectual property& FDA Regulations
Intellectual property has different forms in case of access to medicine, patent is an public policy, where government aims to provide monopoly to a company in the market as an compensation for Research and development and also providing benefits to public in from of technological advancements, extensive patent protection delays and controls the competition in generic drug market ,patent expiry dates are critical for the timing of generic entry into the market.
Related Conference of Patent Access& Intellectual property& FDA Regulations
November 13-14, 2025
28th International Conference and Exhibition on Pharmaceutical Formulations
Paris, France
November 13-14, 2025
21st International Conference on Pharmaceutical Chemistry
Aix-en-Provence, France
November 25-26, 2025
4th World Congress on Medicinal Chemistry and Computer Aided Drug Design
Paris, France
November 27-28, 2025
4th World Conference on Pharma Industry and Medical Devices
Zurich, Switzerland
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3rd International Conference on Current Advances In Pharmaceutical Industry And development
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23rd International Pharmaceutical Sciences & Life Saving Drugs
Bangkok, Thailand
March 24-25, 2026
11th International Conference on Future Pharma and Innovations
Amsterdam, Netherlands
June 08-09, 2026
8th International Conference and Exhibition on Pharmaceutical Development and Technology
San Diego, USA
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25th International Conference on Medicinal and Pharmaceutical Chemistry
San Diego, USA
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26th World Congress on Pharmaceutical Sciences and Innovations in Pharma Industry
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19th International Conference and Exhibition on Pharmacovigilance & Drug Safety
Rome, Italy
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32nd International Conference on Advanced Clinical Research and Clinical Trials
London, UK
November 19-20, 2026
14th International Conference and Exhibition on Natural Products and Medicinal Plants Research
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Patent Access& Intellectual property& FDA Regulations Conference Speakers
Recommended Sessions
- Acceptance of Generic Drugs by People
- Application of Quantitative systems pharmacology (QSP)
- Best Practices & Strategies for Generic Drug Development
- Bioequivalence approaches for complex injectable API and formulations
- Biosimilars
- Challenges of Manufacturing Generic Drugs
- Challenges of Marketing Generic Drugs
- Complex Generic Drug Product
- Current Good manufacturing practices (CGMP)
- Generic Animal Drug
- Modernization of Bioequivalence Standards for Generic Products
- Patent Access& Intellectual property& FDA Regulations
- Pharmaceutical Quality Assurance
- Quality by Design (QbD) for generic drugs
- Super Generic drugs and Bio Betters
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