|
|
|
|
US FDA GMP And Quality System Regulation (QSR) |
|
| |
 |
|
 |
| |
Regulatory Progress
Associates can help you:
- Provide an Overview of the
US Food and Drug Administration
(FDA)
- Discuss the FDA Quality
System Regulations (QSR)
- General provisions of
current Good Manufacturing
Practice (known as GMP or cGMP)
- Responsibility of management
- Conducting audits, taking
corrective action and
documenting results.
Creating design controls: input,
output, validation, transfer,
changes and documentation
- Purchasing and the
evaluation of suppliers
- Identification and
traceability of products
- Dealing with production and
process changes
- Inspection, measuring and
testing equipment
- Acceptance activities
- What to do with
non-conforming products
- Corrective and Preventive
Actions (CAPA).
Labelling, storage, distribution
and installation
- Records and servicing of
products
RPA professionals can have you
up and complying with US FDA
regulations in record time!
Call us
or email us your questions. We'll
get back with a free estimate.
|
|
|
|
|
