Regulatory Affairs Career Guide | Episode 01 - Top 09 Skills for Regulatory Professionals

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 series 'Regulatory Affairs Career Guide' we will unlock the essential skills every regulatory professional needs in today's dynamic landscape! 🚀 Lets dive into this comprehensive career guide tailored for those eager to excel in the regulatory industry. Whether you're just starting out or looking to sharpen your skillset, this video is your roadmap to success.

Channel Introduction- Welcome to PharmaCamp    • Welcome to PharmaCamp with Neha | Reg...  

Series 1 -Regulatory Learnings | Investigational New Drug (IND) Application
   • Regulatory Learnings | Investigationa...  

Series 2-Regulatory Shorts
   • Regulatory Shorts  

Series 3-EU Marketing Authorisation
   • EU Marketing Authorisation  

Series 4-Dare to Lead with Neha | An Interview Series with Pharma Leaders
   • Dare To Lead - An Interview Series Wi...  

Series 5-Orphan Drug Development
   • Orphan Drug Development  

Series 6-Drug Device Combination Products
   • Drug Device Combination Products  


LinkedIn:   / neha-parashar  
LinkedIn Articles on various Regulatory Topics:
1. Regulatory Pathways for Expedited Access of Medicines   / regula.  .
2. Step-wise Regulatory approach for the Paediatric drug Development   / step-w.  .
3. Designing the Global Regulatory Strategy for the Development of Orphan Medicinal Products
  / design.  .
4. Step wise approach for Quality Risk Management (QRM) in pharmaceutical industries   / step-w.  .
5. Step-wise regulatory approach for the assessment of process related impurities in biological products   / step-w.  .
6. Step-wise approach for sterilisation package preparation in regulatory dossiers for biologicals and other liquid sterilised products   / step-w.  .
7. Step-wise approach for regulatory risk assessment of adventitious agents in biologicals products   / step-w.  .
8. Five Step Approach to Assess Equivalency Requirements of Topical Products   / five-s.  .

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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