Services image

Project Services

 

Veracord

4040 Moorpark Avenue

Suite 100

San Jose, CA 95117

Phone: 408-294-5500

info@veracord.com

Project services

Validation services

Compliance services

Placement services

Clinical Services

Medical Device Consulting Services

Project Services

Pharmaceutical companies face a growing list of regulations governing everything from production processes to product labeling and instructions, as set forth by the U.S. Food and Drug Administration (FDA), the European Medicines Agency (EMEA), and Japan's Ministry of Health, Labor and Welfare (MHLW). To sell in these markets, companies must keep pace with new format regulations, such as the FDA's 21 CFR Part II governing electronic records and Structured Product Labeling (SPL), requiring labeling in XML format. In addition, they must meet global regulatory standards to ensuring traceability and accountability in production processes and systems.

Veracord combines a core set of skills with technological expertise matched to your business needs to deliver quantifiable value. Veracord’s global, practical approach to identifying, designing and implementing technology solutions involves working with clients to analyze existing infrastructure and strategic needs, then carefully engineering solutions that deliver tangible and measurable results.

Veracord supports clients in the following areas: