Shiva Shankar Varganti
IDMP | Veeva Vault | Data Governance | Agentic AI
- Role
- Deputy Manager at Aspen Pharma Group
- Location
- Mumbai, MH, IN
- LinkedIn followers
- 500 followers
About Shiva Shankar Varganti
With over a decade of experience in pharmaceutical regulatory compliance and master data management, I have consistently driven innovation within the life sciences sector. As a former member of the Medicines for Europe Telematics WG (SPOR/ISO IDMP task force) and an active member of the IRISS Forum, I’ve shaped and implemented best practices aligned with global regulations. Certified as a Veeva Vault Administrator, my expertise spans IDMP, SPOR, DADI/PLM, IRIS, PQ/CMC, and EU-SRS compliance.I focus on integrating advanced Master Data Management (MDM), Veeva Vault with data analytics to enhance data quality, ensure traceability, and deliver actionable insights for smarter regulatory submissions. Leveraging Make Workflow Automation and AI automation, I optimize compliance workflows and reduce operational overhead. By deploying Agentic AI, I enable proactive monitoring of regulatory changes and autonomous dossier preparation, empowering organizations with adaptive, intelligent systems for superior compliance and agility.
Experience
Deputy Manager
Jul 2024 — Present · Hyderabad, IN
Education
Seventh Day Adventist High School
High School, Matriculation
2004 — 2005
Sri Chaitanya Junior Kalasala
High School, Life Science
2005 — 2007
Maheshwara Institute Of Pharmacy
Bachelor’s Degree, Pharmacy
2007 — 2011
Anurag Pharmacy College
Master’s Degree, Pharmaceutical Sciences
2011 — 2013
Skills
- Management
- Good Laboratory Practice (Glp)
- Medical Devices
- Clinical Research
- Medical Writing
- Idmp
- Arisg
- Meddra
- Microsoft Office
- Sales
- Small Business Management
- Drug Development
- Iso Idmp
- Gcp
- Clinical Data Management
- Healthcare
- Business Development
- Evmpd
- Quality Assurance
- Pharmaceutical Industry
- Sop
- Drug Safety
- Primo
- Ich-Gcp
- Regulatory Submissions
- Research
- Vaccines
- Oncology
- Protocol
- Clinical Trials
- U.s. Food and Drug Administration (Fda)
- Medicine
- Xevmpd
- Training
- Iso 11615
- Regulatory Requirements
- Pharmaceutical Research
- Validation
- Regulatory Affairs
- Lifesciences
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