Pharmaceutical IPR and Regulatory Affairs
Development of a new pharmaceutical product requires at least 15 years because of changes in the regulatory. Regulatory Affairs Department acts as the interface between the pharmaceutical company and the regulatory agencies across the world. Regulatory authorities act a vital role for approval of generics. Regulatory Affairs contributes essentially to the overall success of drug development, both at early pre-marketing stages and at all times post-marketing. Regulatory Affairs professionals can play a key role in guiding drug development strategy in an increasingly global environment. North America and Europe contribute about 57.0% of global pharmaceutical sales. The global regulatory affairs outsourcing market size was valued at USD 4.53 billion in 2016 and is expected to grow at a CAGR of 11.9% over the forecast period.
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Pharmaceutical IPR and Regulatory Affairs Conference Speakers
Recommended Sessions
- Bioavailability and Bioequivalence Studies
- Novel Drug Formulation Procedures
- Pharmaceutical IPR and Regulatory Affairs
- Transdermal & Intradermal Drug Delivery Systems
- Wearable Drug Delivery
- Challenges in Drug Administration
- Drug Delivery approaches for Parenterals
- Drug Delivery Devices: Approaches and Manufacturing
- Drug Delivery Technologies
- Drug Designing and Development
- Novel Drug Delivery Systems
- Pharmaceutical Analysis Methods
- Pharmaceutical Excipients Development
- Pharmaceutical Formulations: Academic and Industry Perspective
- Pharmaceutical Formulations: Types and Novelties
- Pharmaceutical Nanotechnology: Challenges and Opportunities
- Pharmaceutical Research and Development
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