Anand Kodali
Veeva vault | Submission Management | Publishing | Regulatory Affairs | Disability Advocate | PwD
- Role
- Expert in Regulatory Affairs Submission Management at Merck Group
- Location
- Bengaluru, IN
- LinkedIn followers
- 500 followers
About Anand Kodali
Regulatory Operations professional experience of 8+ years. Proficient in Document level and Submission level publishing for all 5 Modules of eCTD for USFDA, EMA and NeeS. Produce regulatory publishing submissions (INDs, NDAs, MAAs, annual reports, Clinical Study Reports and Life cycle management) in accordance with US, Europe and global requirements using electronic publishing tools. Disability advocate, Person with Disability (PwD) Champion & strives for strategies to infuse D&I culture. Good communicator, team player, flexible and quick to adapt new environment /people. Highly organized with strong attention to details who can work efficiently within a time sensitive situation & able to prioritize workloads effectively whilst under pressure both independently as well as working as part of a team. Computer literate using Word Processing Programs such as Excel spreadsheets, PowerPoint presentations etc. Highly experienced in Experience with tools such as eCTDXpress, ISI Publisher, EURS Validator & Lorenz Validator, Oxygen, Viewpoint, eCTD Viewer, Evermap tool, Acrobat plug-in and Link dictionary tool, Excel, Powerpoint, PDF files. And skilled in Advance Excel Certificated, Excel Macro developer and SAS programing learner.
Experience
Expert in Regulatory Affairs Submission Management
Oct 2024 — Present · Bengaluru, IN
Education
Hindu College of Pharmacy
M. Pharmacy
2009 — 2011
KVSR SIDDHARTHA COLLEGE OF PHARMACEUTICA
Bachelor of Pharmacy (B.Pharm.)
2005 — 2009
Seventh Day Adventist High School, Nuzvid
ISC
2003 — 2005
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