Services
Allphase Services
Allphase Clinical Research provides clinical trial management, monitoring, medical writing, auditing, and related regulatory services to pharmaceutical and biotechnology companies. These are our core competencies and as such, they are executed effectively. The experience of our team has been consolidated to develop our organization as an efficient and user-friendly resource for our clients. To ensure that we continue to provide the level of service our customers expect, we regularly survey our clients and investigative sites for feedback.
Affiliate Services
Allphase Clinical Research is able to offer clients additional capabilities by augmenting our in-house services with those of our affiliated partners to be able to provide:
• Central Laboratory Services • Ethics Review Board
• Investigational Product Distribution • Translation Services
• IVRS • Global CRO Network
• Home Health Care • Pharmacovigilance
To see in further detail the services we provide, please follow the links below:
Product Development Planning
Project Management
Clinical Monitoring
Data Management
Operational Support
Investigator Meetings
Regulatory Affairs
Scientific Support and Medical Writing
Drug Safety
Biostatistics
Quality Assurance
ACE Training
Document Storage