Years of experience from both a sponsor’s and a CRO perspective laid the foundation for our world class clinical trial management team. Prosoft’s team can do as much or as little as our clients request of us, managing the entire clinical trial or just assisting in various aspects.

• Investigator contract negotiations
• Critical document collection
• Drug supply coordination
• Timeline development
• Adverse event narrative writing
• Study report completion
• Site audits
• Clinical trial tracking and monitoring
• Vendor contract negotiations

request for proposal

Prosoft Clinical has provided exceptional clinical, data management, CMC, and statistical consulting services on a number of development projects. Their experience and diligence to getting the job right is what distinguishes them from other CROs. I recommend them without hesitation

~ James H Lee MD PhD Group Vice President, Head Inflammation and AutoImmunity Incyte Corporation