Avicemer offers a wide-range of therapeutic expertise and world-class information technology and communication within a unique global corporate structure that delivers exceptional customer service.

 

With more than 30 global locations, Avicemer has access to very diverse patient population. From small local trials to complex multi-site and multi-national programs, Avicemer has the global resources and experience to help Sponsors achieve their goals effectively.

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Phase II/III Clinical Trials

Whether you prefer a turnkey full service support or functional provider service support, we will provide you with the right team, attentive delivery and strong dedication to your goals.

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We may also support you via a CRO/SMO hybrid model.  We are positioned to work with you using the appropriate framework that fits into your study planning and overall strategy of outsourcing. If your policy is to work directly with Medical Centers and Principal Investigators, we will facilitate that for you. In addition to turnkey projects, we can support:

• Accelerated Start-up and Recruitment

• Management and coordination of Central Labs that deliver standardized implementation, analytical testing and database development

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Study management & monitoring

We can manage your clinical study from site initiation through project close out. The following is a partial list of our study management services:

• Project management and planning

• Preparation of study documents

• Conducting investigator and study experts meetings

• Training of personnel

• Management of trial medication

• Sites identification and selection

• Initiation visits

• Monitoring visits

• Close-out visits

• Management of laboratory samples

• Quality assurance

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Phase IIIB/IV and Safety

Late phases and Safety services involve:

• Safety surveillance and observational studies

• Benefit risk analysis services to evaluate potential regulatory concerns

• Clinical safety services including Pharmacovigilance

• Pharmacoeconomics studies and health outcome research

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Patients recruitment and management

Finding, enrolling and retaining study subjects are some of the largest and most costly challenges facing clinical research professionals. The timely enrolment of appropriate subjects into trials is critical to managing the time lines for a development program. We can assist Sponsors:

• Estimate enrolment potential of Sites

• Conduct the right study campaign

• Administer call centers to assist in screening patients and reply to their inquiries

• Maximize retention

• Manage compliance