Personal Information
Organization / Workplace
Vishakhapatnam Area, India India
Occupation
Student at VIGNAN INSTITUTE OF PHARMACEUTICAL TECHNOLOGY
Tags
pharmaceutical
casestudy
management
usfda
drugs
antibiotics
ich guidelines
quality risk management
regulatory affairs
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- Presentations
- Documents
- Infographics
510 k
Mary Roopsy Jino
•
6 years ago
510kvs pma slides
Tahir Rizvi
•
8 years ago
510(k) Pre-Market Notification Project
Brandon MacAleese
•
8 years ago
Accelerated stability studes
Sunil Boreddy Rx
•
10 years ago
Cmc and post regulatory
Dev Jain
•
5 years ago
MDSAP
Dr. Peter Drechsler
•
8 years ago
Understanding the Medical device Single Audit Program (MDSAP) & How to Prepare for It
Greenlight Guru
•
5 years ago
Presentation: Medical Devices Single Audit Program (MDSAP) Pilot Program
TGA Australia
•
7 years ago
FDA Unique Device Identification (UDI) Overview
Caroline Bloemker, M.S., RAC
•
8 years ago
UDI
Pavan Kumar Malwade
•
7 years ago
12 Steps for Medical Device UDI Submissions to the FDA GUDID
Joe Hage
•
9 years ago
Clinical Evaluation Report (CER) - Decode the Step-wise Approach for Compliance
Freyr Solutions
•
5 years ago
FREYR UDI VISION SERIES SESSION 3 - DI & PI
Freyr Solutions
•
9 years ago
FREYR UDI VISION SERIES SESSION 1 - UDI READINESS
Freyr Solutions
•
9 years ago
US DMF v/s European DMF
Neha Pillai
•
6 years ago
Regulatory affairs-Introduction to CTD
Mahesh shinde
•
9 years ago
labelling of drugs and cosmetics in European Union
Bindu Kshtriya
•
7 years ago
Anticounterfeit packaging
MadhuraNewrekar
•
5 years ago
Anti-Counterfeit Packaging Technologies
Bilcare Research
•
13 years ago
Barcodes, RFID or Smart Items? Evaluating track and trace technology today and tommorow
Till Riedel
•
12 years ago