Veritas Research, Inc., an independent Contract Research Organization (CRO), was established in September 2000, to provide quality clinical research to the pharmaceutical and biotech industries in all therapeutic areas. We are experienced in Phase II through Phase IV studies. Our mission is to support our Sponsor partners with personalized service and to add scientific and clinical value to each and every project we undertake. Our extensive knowledge of CRO operations and Sponsor culture give us an edge in creating a progressive and innovative research community. "Truth in Research" is the adage we live by.

We stress proper communication between our staff and our sites to encourage and foster a positive relationship between CRO, Sponsor and investigative sites. This approach provides invaluable rewards to both Veritas and our Sponsor clients. All research is conducted in strict confidence and in compliance with all government and local laws.

In today’s competitive market, we are cognizant that time is the real value. Our focus is to assist our clients in bringing their product(s) to market faster with the integrity that they deserve. Veritas Research is committed to exceeding high standards of performance in everything we do by being responsive and dedicated to the needs of our Sponsors while protecting the rights of human patients.

We offer the following specialized clinical consulting services:

• Strategic Clinical Planning
• Phase II - IV Clinical Trial Management and Monitoring
• Standard Operating Procedures (SOPs) Review and Development
• Project Management Optimization
• Event Planning - Investigator Meetings, Advisory Board Meetings, Focus Groups
• Auditing
• CRAtoolbox™
  • The only PDA-based application designed to assist clinical monitors and study coordinators with calculations and conversions found on a CRF. The 15 most frequently performed clinical research calculations, customized to match your clinical research needs, all together in one place for ease of use.

Penny Blinder, President, has over 20 years experience in clinical research. After mastering all of the related responsibilities as a CRA, Assistant Project Manager and Project Manager over the course of 8 years, she worked her way up to Director of Operations for a mid-size CRO. Penny has overseen the clinical and data day-to-day management and execution of multi-therapeutic, multi-center clinical trials for numerous pharmaceutical and device-manufacturing Sponsors. Her expertise lies in Rx to OTC switch studies, and the design of creative Phase III trials in support of category changes. Current responsibilities include business development and creating synergistic relationships with industry partners.

Stacey Lense, Executive Vice President, has 9 years of clinical research experience with extensive project management knowledge in the areas of gastrointestinal diseases and feminine hygiene care. Stacey has designed, developed and facilitated an entry level training program for CRAs in Good Clinical Practices and monitoring techniques. Stacey's responsibilities included clinical training, daily supervision, project-specific training, resource allocation, measurable tracking and semi-annual performance evaluations. She has developed and implemented CRO Standard Operating Procedures (SOPs), as well as assisted in the development and design of a CRO auditing department. Current responsibilities include operation and management of current Veritas research projects.

• Synergy Research, Inc.
• Clinfosystems
• AXONYX
• Ikonisys, Inc.
• Meditor Pharmaceuticals
• MedecoNovo Research, Inc.
• Wyeth-Lederle Vaccines
• MannKind Corporation

Contact Information

Veritas Research
Penny Blinder, President
138 East Drive
North Massapequa, NY 11758 USA
Phone: 516-850-8240
Fax: 516-293-1518
E-mail:

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