Leucine Software- E-Log Handling


B.Pharm graduate with hands-on experience in pharmaceutical manufacturing at Cipla, seeking to transition into Pharmacovigilance/Clinical Research/ Regulatory Affairs. Eager to apply my understanding of drug safety, ADR reporting, and regulatory compliance to support patient safety and organizational growth.
ADR knowledge
ICSR processing
MedDRA terminology
Drug Safety Awareness
GMP compliance
Standard Operating Procedures
Quality Assurance Fundamentals
Regulatory awareness
Batch Record Review
Microsoft Word & PowerPoint
Problem-Solving Approach
Attention to Detail
Good Communication
CAPA Deviation & Handling
Introduction to Pharmacovigilence & Drug Safety from Biopharma Institute
Leucine Software- E-Log Handling
Sports: Cricket, Badminton, Kabaddi, Kho-Kho
Dancing
Cooking
Exploring New Places
I hereby declare that all the information provided above is true and correct to the best of my knowledge.
Date: ___________ Place: ___________
Abhishek Madheshiya
Introduction to Pharmacovigilence & Drug Safety from Biopharma Institute