Clinical Manufacturing Services

Pharma One Resources can provide expertise for your Clinical Trial materials (CTM) by implementing and maintaining communication to ensure on-time processing and delivery of clinical supplies for domestic and international studies by identifying key, rate limiting tasks and preventing delays in the supply process.

We work synergistically to ensure proper CTM use through effective and efficient packaging and labeling and other areas:

• Pharmaceutical technologies
• Stability Studies
• Clinical Trial Manufacturing
• Clinical Packaging Design and Kit Assembly
• Document management
• SOP

Pharma One will assist with the development/review of the bulk CTM requirements for Clinical Trial, Stability, QC Testing, Release, Packaging and labeling requirements by addressing stability including Storage and Re-assay data that impact the CTM process.

We do assist with coordinating timely manufacture and delivery of bulk CTM ensuring complete documentation and tracking of all services provided..

Support Services

 We offer the following additional services:

• Project Management
• SOP Development
• Tech Transfer & Protocol Review

In addition, Pharma One staffing Division offers qualified pharmaceutical professional for staff augmentation to support your short term or long term internal needs.

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