Clinical trials protocols.
Blackwell’s electronic medical record allows to record the medical follow-up of patients attending the research centers according to current pharmaceutical industry standards, as well as compliance with Good Clinical industry standards, as well as compliance with Good Clinical Practice (GCP). (GCP).
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Modernize your clinical research management protocols, BLACKWELL has the most efficient way to solve all your needs.
BLACKWELL's platform
is designed according to Mexican data protection and privacy laws, since no record can be edited without the patient’s authorization, which must be signed and uploaded to the platform in all records.
In Blackwell the physician and/or clinical protocols staff capture patient information in the same way as if they were doing it on paper.
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Collaborating with the best health practices in Mexico.
It is designed to comply with the Mexican Official Standard NOM-004-SSA3-2012, On the clinical record, as well as with the Mexican Official Standard NOM-024-SSA3-2012, Registration Information Systems.
