This course will cover the following topics:
                                            - Effective compilation of CTD and critical review of documentation
- Quality by design, critical attributes and developing new product using the CQA pyramid model
- Compiling and submitting Module 3 (CTD) of your registration dossier
- Identifying the extent of content expected by EU and US regulators
- Achieving the quickest turnaround of your submission
- Managing the pharmaceutical development and quality aspects of your developments and registration dossier in Europe and US
- Ensuring right first time development
- Meeting the legal framework and guidelines for the CMC / quality part of the dossier, and links to GMP

 
             
             
                             
                         
                         
                                 
                                         
                                                                     
                                                                                                                         
                 
            