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What are the Steps and Timelines for Decentralised Procedure and Mutual Recognition Procedure?| DRA
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Welcome to the PharmaCamp with Neha. This is a small initiative from my side to share knowledge about the pharmaceutical world and regulatory, as I feel education is the best gift one can receive or give back to society.
Are you a working professional who wants to upgrade your skills? OR a student who wants to make a career in pharmaceuticals? OR are you a person who is interested to learn about the regulatory systems? Then this YouTube channel is for you.
About me:
I am Neha Parashar, working as a Associate Director in a pharmaceutical company and based in Germany. I am a passionate healthcare professional, an educator, and a mentor.
In this video, we will discuss - What are the Steps and Timelines for Decentralised Procedure (DCP) and Mutual Recognition Procedure (MRP)?
Series 1 -Regulatory Learnings | Investigational New Drug (IND) Application
Series 2-Regulatory Shorts
Regulatory Shorts#2 | DSUR vs PSUR | Safety Reports
Series 3-EU Marketing Authorisation
LinkedIn Articles on various Regulatory Topics:
3. Designing the Global Regulatory Strategy for the Development of Orphan Medicinal Products
Disclaimer- This video channel is for educational purposes. These are purely my views and not any recommendations. The channel does not represent the views of the organization I am associated with, and it has no connection with my current organization.
Are you a working professional who wants to upgrade your skills? OR a student who wants to make a career in pharmaceuticals? OR are you a person who is interested to learn about the regulatory systems? Then this YouTube channel is for you.
About me:
I am Neha Parashar, working as a Associate Director in a pharmaceutical company and based in Germany. I am a passionate healthcare professional, an educator, and a mentor.
In this video, we will discuss - What are the Steps and Timelines for Decentralised Procedure (DCP) and Mutual Recognition Procedure (MRP)?
Series 1 -Regulatory Learnings | Investigational New Drug (IND) Application
Series 2-Regulatory Shorts
Regulatory Shorts#2 | DSUR vs PSUR | Safety Reports
Series 3-EU Marketing Authorisation
LinkedIn Articles on various Regulatory Topics:
3. Designing the Global Regulatory Strategy for the Development of Orphan Medicinal Products
Disclaimer- This video channel is for educational purposes. These are purely my views and not any recommendations. The channel does not represent the views of the organization I am associated with, and it has no connection with my current organization.
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