The key to a successful trial.
VetPharm’s unique and comprehensive study management system, which is thoroughly documented in our standard operating procedures, runs faster, smarter, and smoother than anything most sponsors have experienced. By outsourcing their clinical trials to VetPharm, they insource better data, in less time, and at lower total cost. As a result, their new products get approved faster and launched sooner. And that means larger market shares, longer revenue cycles, and higher profits.
Complete Planning and Design Services
- New product development plan
- FDA/CVM liaison
- Protocol development and review
- Data form (CRF) design, review, and testing
- Electronic data capture (EDC) database design and user acceptance testing (UAT)
- Pre-study enrollment projections
- Standard operating procedures (SOPs)
- Good Clinical Practice (GCP) training and testing
- Regulatory compliance
- Investigator and site selection
- Investigator and site staff training
- Pre-study site qualification inspection
- Investigator meeting organization and travel coordination
- Investigator binder design, production, and distribution
- Owner diary design, production, and distribution
- Laboratory selection and contract negotiation
- Drug packaging, labelling, storage, and distribution
- Test article accountability system
- Safety, palatability, pilot, pivotal, and post-marketing studies
If you’d like to know more about VetPharm’s unique and comprehensive study management system, current clinical trial opportunities, employment opportunities, or to discuss the conduct of a specific clinical trial, please send us a message.