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We are a full-service consulting firm for medical professionals, specializing in clinical trial site management.

Our clinical trial management services include the startup and management phase I-IV trials. We offer complete training and ongoing support for new physicians and study coordinators. We currently have ongoing trials for cardiovascular, dermatology and endocrinology. Our expert staff manages regulatory, patient recruitment and source documents.

Staff Experience:

- Our staff includes Registered Nurses, Medical Assistants and support staff with over 25 years of clinical trials experience.

- Our research staff are certified by ACRP ( Association of Clinical Research Professionals)

- Our staff possess a high degree of professionalism, involvement and service. The Bracane Company is dedicated to providing  exceptional customer service.

Our Investigators:

- Conduct clinical trials according to FDA regulations and ICH guidelines.

- Maintain protocol records, screening logs and other required documents in accordance with FDA regulations and the sponsor requests.
 
- Participate in training programs selected by the company for clinical trial management and FDA regulations.

Benefit to the sponsor:

- Principle Investigator selection is fast, efficient study start-up.

- Regulatory documents submission and management.

- Individual site recruitment plan.

- Training programs for the principle investigator and research staff on an ongoing basis for "Good Clinical Practice Guidelines" and Food and Drug Administration (FDA) code of regulations.

- Experienced research staff on site to assist with trial procedures and management.

- Ongoing quality assurance and site audits for compliance.

 

Our mission is to fulfill our client's clinical research needs by being reliable, efficient and consent. Operating at the highest level of integrity and provide the highest quality of service, while providing an environment of reward and growth for internal customers and aid in the development of effective, safe products for mankind.

The Bracane Company provides clinical trial management for therapeutic categories for pharmaceutical manufacturers and biotechnology companies for clinical trials phases I-IV.

Interested in becoming a study coordinator or a monitor? With things constantly changing in the medical field do you find yourself needing additional training and support?

Weather you are a contract CRA or a business owner who cannot afford the cost of hiring a full time trainer. The Bracane Company has the right solution for you. We offer training for both

- Study Coordinators

- Monitors

Our courses cover:

- Good Clinical Practices

- FDA rules and Regulations

- Protocols

- Monitoring guidelines

- Report writing

- and many more

 

For more information please contact:

The Bracane Company

Ph: 972-422-5674

Fax: 972-881-4292

 


 

 

 

Clinical Areas of Research

- Diabetes

- Asthma

- Hypertension

- Oncology

- Woman's Health

- Osteoporosis

- Pain Management

- Dermatology

- Anti-infections

- Endocrinology

Our Clients and Customers

- Novartis Pharm...

- GlaxoSmithKline

- Sanofi-Aventis

- ICON

- OmniCare

- Luitpold Pharm

- Medpoint

- Takeda

- PPD

- Nereus Pharm

- Gilead Science Inc

- TX Department of Assistive and Rehabilative Services

- TX Department of State Health Services

- and others

 

 

The Bracane Company

101 E Park Blvd Ste 600

Plano, TX 75074

Phone:

972-516-3809

Fax:

972-727-6239

Email:

pjnelson@bracaneco.com

 

The Bracane Company ©2009

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