Labeling, Packaging & Distribution of Clinical Supplies

Fast, flexible GMP compliant clinical labeling on the West Coast, with no study too small!

Trusted Provider of Quality Clinical Labeling & Distribution

Accurate labeling of your clinical supplies is of critical importance to your Program. Our clients rely on the experienced labeling and distribution team at Dow to label their supplies accurately every time and to deliver those supplies to the clinical sites on time. The labeling group works closely with the Quality Assurance Department to make sure this happens. Accuracy, personalized service and meeting deadlines is our business.

 

Flexibility & Responsiveness

Whether your needs are for small Phase I open-label studies or large, multi-center, complex Phase 3 studies, Dow designs and executes an appropriate program for the management of your important clinical supplies. Dow’s labeling group is very responsive to new and existing clients and can quickly meet the needs for small projects as well as large. We specialize in the customization of patient kits for maximum patient compliance for any dosage form, and can label a large range of container sizes. Any storage condition can be met to support labeling operations.

GMP Facilities on the West Coast with Multi-National Capabilities

Dow's state-of-the-art laboratory facility is located in the biotech hub of Northern California. Operating under cGMPs, Dow has designated rooms for pharmaceutical labeling, staging, in-process holding and kit assembly. Any storage condition can be met to support labeling operations. The facility is also licensed to handle and store schedule 3-5 drugs.

While our operations are located in Sonoma County, California, Dow is experienced with label design in multi-national languages and has distributed labeled supplies to over 40 different countries. We are acutely aware of worldwide regulatory requirements.

Full Complement of Services Offered:

  • Label Design – specifications, printing, multi-national languages
  • Random Code Design and Control
  • Patient Kit Design
  • Labeling Types – open label, blinded, double-blind, double-blind cross over
  • Storage – temperature controlled conditions
  • Distribution – national and global
  • Returned Drug Accountability and Destruction
  • QC Testing & QA Release
  • Full GMP Documentation

To Learn More

Please contact Karen Hanley, Assistant Director, Business Development & Client Relations, (x 654) for additional information. We encourage you to visit our facilities and evaluate our operations. Tel: 707.793.2600