top of page

Late Phase Research

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

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



Phase II/III Clinical Trials

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

We also provide support via a CRO/SMO hybrid model.  We are positioned to work with clients using the appropriate framework that fits into their study planning and overall strategy of outsourcing. If our client's policy is to work directly with medical centers and principal investigators, we collaborate accordingly. In addition to turn-key projects, we support:

  • Accelerated start-up and recruitment

  • Management and coordination of central labs that deliver standardized implementation, analytical testing and database development



Study Management & Monitoring

We 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/investigational product

  • Site identification and selection

  • Site initiation visits

  • Monitoring visits

  • Close-out visits

  • Management of laboratory samples

  • Quality assurance



Phase IIIB/IV & 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



Patient Recruitment & Management


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

  • Estimate enrollment 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

bottom of page