Regulatory Affairs

1.Abbreviated New Drug Application

2.Clinical Trials

3.Documentation

4.General Agreements on Tariffs and Trade 

5.GMP Guidelines 

6.GMP and cGMP Considerations 

7.Good Laboratory Practice

8.Intellectual Property Rights 

9.Intellectual Property Rights-2

10.ISO 9000 Quality Management Systems

11.New Drug Applications 

12.Patents Final 

13.Total Quality Management