Pharmaceuticals (21 CFR Part 210, 21 CFR Part 211 and related Regulations)

V
Where & How to Capture Details of Periodic Reviews of Change Control & CAPAs
Replies
8
Views
4K
v9991
V
J
Transitioning from ISO 9001 to CFR - Recently transferred to a Pharma company
Replies
9
Views
4K
AnaMariaVR2
AnaMariaVR2
D
Printed Packaging Material Suppliers to Pharmaceutical Companies
2
Replies
13
Views
8K
ScottK
ScottK
D
Requirements to Manufacture a Pharmaceutical vs. Medical Device
Replies
9
Views
5K
mehtagaurav_2004
M
R
Inquiry for License needed when not releasing your self? Pharmaceutical Products
Replies
1
Views
2K
Marc
Marc
P
Incoming (Receiving) Components Inspections
Replies
1
Views
4K
Stijloor
Stijloor
G
Dose Audit Requirements
Replies
7
Views
6K
Kees Fremery
K
R
Pantoprazole Enteric Coated, Gastro Resistant & Delayed Release Tablet differences
Replies
4
Views
16K
Jim Wynne
Jim Wynne
J
Environment Monitoring programme for pharmaceutical industry
Replies
4
Views
6K
bio_subbu
bio_subbu
L
Recall Process for Pharmaceuticals - Example wanted
Replies
9
Views
8K
amodra
A
AnaMariaVR2
Nanodrop Spectrophotometer
Replies
3
Views
7K
12stones
1
AnaMariaVR2
Laboratory Equipment Quality System - Calibration, Maintenance and Inspection
2
Replies
10
Views
7K
AnaMariaVR2
AnaMariaVR2
D
Ventilation equipment- Are there any FDA or pharmaceutical industry requirements
Replies
1
Views
2K
PotentCompoundSafety
P
V
Concepts and Industry Practices of Measurement-Metrics-QA (Pharma/Device Industry)
Replies
2
Views
3K
v9991
V
S
GMP guideline for Manufacturing of Inhaled Dosage Forms
Replies
2
Views
4K
shraddha13
S
You must log in or register to post here.
Top Bottom