Hello Everyone,
I recently join the membership of RAPS to learn more about regulatory updates and to connect with RA professionals globally . I would love to be volunteer for the RA- Ontario chapter.
I have 3+ years of experience in RA in pharmaceutical industry and I hold master's in regulatory affairs so I am well aware with drug development process, product lifecycle management, Non-clinical, clinical and CMC part of dossier and DMF. I have good practice to work on CTD format.
Kindly please let me know if I can contribute my skill and knowledge for any volunteer opportunity for Ontario chapter.
Thank you and have a good day to all!
Best regards,
Samira
------------------------------
Samirabanu Shaikh
N/A
Toronto ON
Canada
------------------------------