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Hi everyone,

I hold master's in regulatory affairs in drugs,biologics and medical devices from Northeastern university , Toronto. Apart from this, I have 3+ years of experience in regulatory field in pharmaceutical industry. 

Summary of previous experience and knowledge:

·       3+ years of experience as a regulatory professional in pharmaceutical industry, Master's in science in Regulatory affairs in drugs, biologics and medical devices.

·       Expert knowledge of regulatory guidance and requirements, drug development process, Product lifecycle management, Pharmaceutical manufacturing, USFDA, HC, ICH, GLP, GMP and Good clinical practice.

·       Expert with format of NDA, NDS, CTA, IND, ANDA (generics), DMF (CMC).

·       Experienced with Dossier preparation: in CTD, ACTD and country specific format.

I graduated on July 2022 and I have been looking for full time opportunity in field of regulatory affairs in Canada. Please feel free to reach out to me on email ID : samfallvibe@gmail.com