A Protocol describes the objectives, design, methodology, statistical considerations and organization of a Clinical Study, BRCR Global has highly qualified personnel in the preparation and development of an instrument according to the needs of the client"
The indispensable variables for the design of our protocols are the following:
• Type of participant
• Test schedule
• Standard Operating Procedures
• Medications and doses
• Test duration
Protocols (among many other documents produced as part of a test) must be controlled documents; numbered and dated version using a formalized convention.
To help researchers develop effective and high-quality protocols, BRCR Global has designed a protocol guide and a template which optimize the consistency and quality of the result.
Protocols (among many other documents produced as part of a test) must be controlled documents; numbered and dated version using a formalized convention.
We have extensive experience in a variety of therapeutic areas by managing studies in USA, Latin America, Caribbean Islands and Central America. We have built strong business relationships with main researchers in several cities in the referred regions.
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