Kumari Priyanka

FAQ About Kumari Priyanka

• What is Kumari Priyanka's address?

  Kumari Priyanka is located at
  Hyderabad, Telangana, India

• What is Kumari Priyanka's job title?

  Kumari Priyanka is a
  A proven track record as a regulatory professional, Priyanka has played a significant role in the creation and implementation of International Package Leaflet (IPL) and relevant SOP updates. She has contributed to relevant sections of the Periodic Safety Update Reports (PSURs) and Addendum Reports (ARs) to ensure current information is submitted to health authorities. She supports Core Data Sheets (CDS) updates to help achieve international harmonization of pharmaceutical product information. Together with this, she has experience in preparation and submission of product registration dossiers including Biotech products as per the marketing requirements for regulated market, preparation of Certificate of Pharmaceutical Products (COPP) to be submitted to local FDA for approvals and in audit and compliance activities. Her experience in working in different parts of the country and with people across the world has given her holistic view of cultural diversity at work. As an individual she values integrity, openness and collaborative approach Specialties: Global & European Regulatory Affairs, Health authority queries, PSUR, CDS, Process excellence, Project Management, GMP/Compliance, CTD preparation & submission, administration and leadership, Audit, SOPs Novartis

• What industry does Kumari Priyanka currently work in?

  Kumari Priyanka currently works in the
  Novartis

• What is Kumari Priyanka's area of expertise?

  Kumari Priyanka specializes in
  A proven track record as a regulatory professional, Priyanka has played a significant role in the creation and implementation of International Package Leaflet (IPL) and relevant SOP updates. She has contributed to relevant sections of the Periodic Safety Update Reports (PSURs) and Addendum Reports (ARs) to ensure current information is submitted to health authorities. She supports Core Data Sheets (CDS) updates to help achieve international harmonization of pharmaceutical product information. Together with this, she has experience in preparation and submission of product registration dossiers including Biotech products as per the marketing requirements for regulated market, preparation of Certificate of Pharmaceutical Products (COPP) to be submitted to local FDA for approvals and in audit and compliance activities. Her experience in working in different parts of the country and with people across the world has given her holistic view of cultural diversity at work. As an individual she values integrity, openness and collaborative approach Specialties: Global & European Regulatory Affairs, Health authority queries, PSUR, CDS, Process excellence, Project Management, GMP/Compliance, CTD preparation & submission, administration and leadership, Audit, SOPs

• Which languages does Kumari Priyanka speak? 

  Kumari Priyanka speaks the following languages:
  No languages available.

• Which industries has Kumari Priyanka previously worked in?   

  Kumari Priyanka has prior experience in the following industries:
  Novartis , Cadila Pharmaceuticals , Cadila Pharmaceuticals , Apollo Hospitals

• What is Kumari Priyanka’s work experience?  

  Kumari Priyanka has the following professional experience:
  Novartis , Cadila Pharmaceuticals , Cadila Pharmaceuticals , Apollo Hospitals .

• How can I find Kumari Priyanka on LinkedIn?  

  You can view Kumari Priyanka’s
  LinkedIn profile at LinkedIn URL.

• What are Kumari Priyanka’s work email addresses?  

  Kumari Priyanka’s work email addresses are
  [email protected] .

• What company does Kumari Priyanka work for?  

  Kumari Priyanka works at
  Novartis