GML is frequently contacted by pharmaceutical, biopharmaceutical,
biotechnology, medical devices companies, logistics industry, CCO’s,
CRO’s looking for immediate access and reference of investigators in
different therapeutic areas, eager and willing to participate in research
projects.
GML Investigators Data Base affords investigators the opportunity to
increase the participation of their site in feasibility processes to be
considered for clinical trials conduction. Please complete the
following preliminary information questionnaire that GML will need,
to recommend you as potential Investigator – Site to healthcare
research companies.
For pharmaceutical and research companies, timelines and quality of response during a feasibility process are key and competitive aspects to advance participation in a research project, GML can support Sites to improve times as well as the quality of feasibility information for a sponsor – regulatory process and local requirements as well as feasibility and capability to carry out the project.
·Imports
·GMP compliant Storage according to temperature and humidity required conditions
·Site distribution including accountability during project up to destruction
Preparation and submissions the applicable regulatory entities, Ethics Committees and Health authorities.
“Interested in participating as Investigator in Clinical Trials” (complete only if you are a Physician/Investigator not for site staff)
Ready to start your next project with us? That's great! Give us a call or send us an email and we will get back to you as soon as possible!
+502 2261 7400
+502 2295 9234