 |
Validation Solutions
| |
 |
Why PVSR?
|
| Our experienced professionals
are dedicated to meeting your project needs in a
timely fashion. Every associate is certified in
our 30 hour Qualification Program. We will work
with you in equipment and facility design review,
computerized system validation, aseptic processing
design, calibration programs, environmental monitoring
programs, Clean Room Certification, GMP audits and
sterilization processes. |
| We
will meet with you and deliver cost effective solutions. |
|
|
|
 |
| |
 |
We
have the whole solution. |
|
|
|
We can provide your organization
with a full range of validation professionals
whose backgrounds include engineering, computerized
systems, biochemistry and microbiology. PVSR is
a single source provider of extensive industry
and technical experience.
|
 |
We can
be there for you! |
|
Let us plan your FDA compliance strategy and
reduce your risk. We provide you with research
and analysis of the latest trends and developments
in compliance, enforcement and regulatory
affairs. |
| Need
Solutions?:
solutions@pvsrwebsite.com |
|
|
|
|
|
 |
| |
| |
 |
Our Capabilities
|
|
PVSR personnel and management has broad
experience in sterile equipment and facilities
we were part of the Schering-Plough Manati
effort to comply with the FDA Concern Decree
requirements. Our Management and/or Associates
have work with: Abbott, Amgen, Aventis,
Biovail, Lilly, Merck & Co, Pfizer, Schering-Plough,
St. Jude Medical, Wyeth and more... Our
resume on-line capability and information
system based structure allow us to be flexible
and agile to fulfill our client needs, we
provide just as our name states, validation
solutions.
|
|
|
|
|
|
 |
