- Regulatory Affairs
- Regulatory & Pharmacovigilance
- Clinical Affairs & Regulatory Strategies
- Regulatory Cooperation and Reliance
- Pharmaceutical Regulatory Environment
- Regulation and Global Regulatory Affairs
- Biologics and Biosimilars
- Best Industry Practices
- Intellectual Property Rights
- Marketing Authorizations-Affordable Healthcare and Fair Trade
- Medical Device & Combination Products Regulations
- Regulatory Strategies and Developments
- Regulatory Requirements for Pharmaceuticals
- Entrepreneurs Investment Meet
- All accepted abstracts will be published in respective OMICS International Journals.
- Abstracts will be provided with Digital Object Identifier by Cross Ref.