|
cGmp
Validation L.L.C– The Company
Established in June 1997, cGMP Validation L.L.C. has 140 employees
based throughout the United States and is a full service validation/compliance
firm offering validation and compliance services for the pharmaceutical,
biotechnology, biologics, medical device, and medical diagnostic
industries. cGMP Validation is staffed with a group of professionals
with considerable experience within the pharmaceutical industries.
The educational disciplines of the team members consist of chemistry,
microbiology, engineering, pharmacy, and computer science. Most
project managers hold graduate degrees, have held senior level
positions in industry and have more than 20 years of pharmaceutical
experiences.
With corporate offices in Mission, Kansas, USA, the team has
performed successful projects throughout the United States and
in Canada, Korea, Italy, India, Germany, and the Netherlands.
cGMP Validation clients have been large, small and medium sized
pharmaceutical (finished and bulk), biological, device, and diagnostic
manufacturers. Projects have ranged in size up to complete validation
of new facilities and processes. All projects, regardless of size,
are given the same professional attention and management.
cGMP Validation L.L.C. is an industry leader with a proven approach
to Validation and GMP Compliance consulting. cGMP Validation provides
industrious and experienced consultants who complete projects
on time and on budget. Emphasis is given to strong project management
and innovative thinking that enhances the quality and value of
out services.
cGMP Validation can look at you company’s unique situation
objectively, uncover your needs and priorities, clearly defined
project requirements, and tailor our services accordingly by using
practical approaches to validation, providing excellent customer
service, and strong project management.
cGMP Validation, L.L.C. has performed more than 600 validation
projects in the last 5 years and written more than 10,000 validation
protocols. Approximately 80% of cGMP Validation’s work is
full facility commissioning and validation of process utilities,
process equipment, analytical equipment, process validation, cleaning
validation, computer validation (including 21 CFR Part 11 assessments
and remediation planning) for large pharmaceutical clients including
Wyeth, Amgen, Eli Lilly, Baxter Heathcare, and Merck. cGMP Validation
has more than 100 clients in finished pharmaceuticals, active
pharmaceutical ingredients (API), biotechnology, biologicals,
diagnostics, and medical devices industries.
|
Sub Menu
Products/Services
Contact
Us
Visit Our Website
Address
|
cGmp Validation L.L.C |
| |
5800 Foxridge Dr, |
| |
Suite 402 Mission,
KS 66202, |
| |
USA |
| Tel. |
+1 913 384 2221 |
| Fax |
+1 913 384 2252 |
|