- Presentations
- Documents
- Infographics
Parenteral production and aseptic area
Shaik Sana
•
9 years ago
Crystal powder zinc sulphate heptahydrate -rech chemical co. ltd
Rech Chemical
•
7 years ago
Flow chart of manufacturing of dyes
Azmir Latif Beg
•
8 years ago
5991 0165 en-1
Bibiana Portillo
•
7 years ago
Column choices feb2008
Gopal Pawar
•
11 years ago
Pharma Regulatory Affairs in Mexico
María Inés Guaia
•
10 years ago
C5 eCTD Summit: Electronic submissions and the new Variations Regulation
seront
•
13 years ago
Dossier Management and Regulatory Affairs.
Naila Kanwal
•
8 years ago
Quality and Regulatory Affairs
MaRS Discovery District
•
16 years ago
Preparing Compliant eCTD Submissions
Scott Abel
•
15 years ago
ctd and e ctd submission
Rohit K.
•
8 years ago
Stability testing and shelf life estimation
Manish sharma
•
9 years ago
Understanding FDA Requirements Medical Devices
marchell
•
15 years ago
Ich guidelines for stability studies 2
priyanka odela
•
11 years ago
ICH GCP
PAREXEL International Clinical Research
•
14 years ago
Preparing a drug registration for the US and the EU: Parallel or sequential applications? – Part 2
Voisin Consulting Life Sciences
•
7 years ago
Pharma regulatory affairs
Girish Swami
•
11 years ago
ANDA filing
debangshuroy89
•
12 years ago
Stability study as per ich guideline
RaKesh Rathava
•
10 years ago
Anda registration in us eu
Patel Parth
•
11 years ago