Presentation Title 2
Presentation Title 2
and Regulations
Slide 4: Immunotherapy
Slide 9: Conclusion
1. FDA Guidance Documents – Provide insights into the regulatory requirements for
cancer drug development and approval.
2. Clinical Trial Protocols and Consent Forms – Outline ethical considerations and
regulations for conducting clinical research.
3. Patent Filings for Cancer Therapeutics – Examples of intellectual property protections
for new cancer treatments.