Top > 
| 321. |
PRI Group
|
|
|
Provides specialist advice for regulatory strategy in Europe.
Date Added: Jul 19, 2006 Hits:
|
|
|
| 322. |
ARX - Digital Signature Solutions
|
|
|
21 CFR Part 11 compliant digital and electronic signatures for any file format, document system, or web application.
Date Added: Jul 19, 2006 Hits:
|
|
|
| 323. |
Solutions MDI, Inc.
|
|
|
clinical affairs, quality systems, compliance strategies, CE mark and FDA submissions.
Date Added: Jul 19, 2006 Hits:
|
|
|
| 325. |
Valid Ground
|
|
|
Valid Ground offers services to cover most aspects of Good Clinical Practice compliance initiatives. We serve pharmaceutical, biotech, and medical device companies, academic institutions, institutional review boards, and contract research organizations.
Date Added: Jul 19, 2006 Hits:
|
|
|
| 326. |
Validation in Partnership Ltd
|
|
|
Specializing in the provision of validation and CGMP (Current Good Manufacturing Practice) compliance services.
Date Added: Jul 19, 2006 Hits:
|
|
|
| 327. |
Cro.nu
|
|
|
CRO in drug development process in close collaboration with the preclinical and clinical departments of pharmaceutical and biotech companies.
Date Added: Jul 19, 2006 Hits:
|
|
|
| 328. |
Training-HIPAA.net
|
|
|
Provide HIPAA compliance kits, manuals, training, security compliance templates and compliance consulting services.
Date Added: Jul 19, 2006 Hits:
|
|
|
| 329. |
nFocus Technologies ERP for Life Sciences
|
|
|
nFocus Technologies has developed a portfolio of software solutions to meet the unique requirements of this highly regulated industry.
Date Added: Jul 19, 2006 Hits:
|
|
|
| 330. |
Samarind Regulatory Management Software
|
|
|
Samarind RMS is a software package for the pharmaceutical industry that manages regulatory affairs and licence submissions.
Date Added: Jul 19, 2006 Hits:
|
|
|
|
|
