Project Management Services & Products
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Medical & Regulatory Affairs
3/4/2016
Taking new products successfully through clinical development, submission and approval can be a difficult, expensive and lengthy process. SynteractHCR’s medical regulatory affairs group offers a wide range of services that spans the full range of product development, including training, performed by senior regulatory professionals with experience in pharmaceutical, diagnostic, device and biotechnology industries. Our medical regulatory affairs team is here to deliver on aggressive timelines and control costs, while ensuring compliance and patient safety.
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Strategic Resourcing Functional Services
5/29/2013
Our dedicated functional teams have the experience to be your partner in clinical research. We deliver a variety of clinical development services customized to fit your objectives, whether you need a single function across several drug programs, a range of functions within a single therapeutic area, a complete staff lift-out or any other defined need.
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Phase I-IIA Clinical Trials
5/29/2013
INC Research/inVentiv Health conducts Phase I-IIa clinical trials quickly and efficiently at its dedicated 22,000 square foot clinical facility comprising more than 200 beds in four independent units. An extensive database and relationships with leading hospitals ensures rapid recruitment of study participants for a wide variety of trials.
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Oncology Clinical Trials
5/29/2013
The unique patient populations, study design challenges, and special endpoints associated with oncology trials demand specialized knowledge. INC Research/inVentiv Health's Oncology team is uniquely qualified to manage that complexity.
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Phase IIb-III Clinical Trials
5/29/2013
With decades of experience in clinical trial design, INC Research/inVentiv Health offers a full range of clinical trial services including bioanalysis, biostatistics, data management, feasibility studies, global safety and pharmacovigilance, medical writing, project management, protocol and case report form design, quality assurance, regulatory affairs, risk management, site management, strategic planning, and study monitoring.
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Central Laboratory Solutions
4/23/2013
Remember the time when laboratory kits were ordered and reordered by sites faxing in pieces of paper, and laboratory reports were faxed and express mailed to investigative sites around the world? Sadly that time is still here for many central laboratory providers.
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Strategic Clinical Project Outsourcing
8/28/2012
RDP Clinical specializes in building highly experienced project monitoring teams that are a custom fit for your specific study demands/ needs that are geographically positioned in direct proportion to the site locations to maximize efficiency.
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Clinical Project Management
5/17/2012
Marken’s intensive project management approach means that your project moves seamlessly through the clinical trial process.
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Project Management
6/24/2011
An exceptional Project Management approach lays the foundation for every successful clinical trial. And by successful, we mean more than just completing the project on-time and on-budget.
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Clinical Project Management
Setting high expectations and exceeding them
For more than 30 years, Rho has helped pharmaceutical and biotechnology companies successfully lead their clinical research projects from initiation to closure. Our Project Managers have years of experience managing clinical trials and programs, including decentralized and virtual trials, in our therapeutic areas of expertise, including Neurology, Psychiatry, Analgesia, Rare Disease, and Infectious Disease and Vaccines. This experience has also given them broad knowledge of clinical research which helps to unify their trial teams and deliver results that are within the desired scope, timeline, and budget.