• Services
Clinical Development Solutions
Clinical Monitoring
Data Management
Biostatistics & Programming
Medical Writing
Regulatory Affairs & Consulting
Pharmacovigilance
Medical Devices
Emerging Biotech
Global Alliance Services
Our Quality Policy
"Quality is our way of life… At inVentiv Clinical Solutions, we are committed to providing superior clinical research services in support of our clients' clinical development pipelines. We believe that the only way to achieve quality excellence is to build it into our systems and processes while investing in training."
click here to learn more about our Quality Policy
Company News
Fortune Magazine rates inVentiv Health #15 of the Fastest Growing Companies.
click here to learn more
inVentiv Clinical Development Solutions
inVentiv Clinical offers a wide range of clinical development services, from full-service clinical trial management to functionally based services to meet both short- and long-term goals. We are committed to providing superior clinical research services through quality excellence in our systems and processes. Our Global Alliance Services in India, Latin America and Europe provide added time zone coverage, accelerated ramp up and strong, cost-effective execution for your clinical development needs.
Click on the links below to find out more about each of our clinical development service offerings.
Protocol/study design
Investigator selection & recruitment
Patient recruitment & retention
Investigator meeting planning
Clinical development plans
Clinical monitoring
Data management
Biostatistics & programming
Medical writing
Regulatory affairs
Pharmacovigilance
Medical Devices
Emerging Biotech
Global Alliance Services

Commitment to Communication

We are committed to providing effective communication throughout every project. We develop a Project Plan at the beginning of every program to identify the informational and communication needs of all parties (Sponsor, Site, Recruiters, Patients, etc.) and suitable means of meeting those needs. This Project Plan identifies study specifics (eg, the process for Investigator selection, site contacts, monitoring intensity, data management plans, etc) and gives a thorough risk analysis with proactive contingency plans. The Project Plan also includes a detailed flow chart of all project activities, including a definition of the responsibilities of team members in addition to the status of the project budgets, timelines and achievements.

Project Management

We assign a Project Manager to each project as the primary point of contact for all project-related questions or concerns. Our Project Managers bring an average of 15 years of experience in clinical research operations, ensuring that your project runs smoothly and efficiently. iCS Project Managers have regular communication with the Sponsor's project lead to discuss progress as well as the technical interface with statisticians, data managers, clinical trial managers, etc. as needed to carry out the day-to-day aspects of running a trial. In addition, our executive leaders are available at all times to help mitigate risks and resolve issues quickly.

Our Experience

inVentiv Clinical brings a wealth of experience from all clinical phases of development and major therapeutic indications, including Oncology, CNS, Cardiovascular, Infectious Disease/HIV and Obesity. In addition, our research experience extends to numerous types of medical devices, including industry-leading experience in neuro-stimulating devices.
*“Other” includes Hematology, Gastroenterology, Respiratory, Urology, Dental, Musculoskeletal
For a further breakdown on our experience as it relates to your clinical development pipeline, please contact us today!
General Capabilities Brochure
Home | Services | About | Careers | Library | Investigator | Contact Us | Sitemap
inVentiv Investor Relations | Terms & Conditions | Smith Hanley Consulting | MedFocus
©Copyright 2007 inVentiv Health
inVentiv Clinical