Consulting and assistance for the complete design of clinical research documents in compliance with International Good Clinical Practices (GCP’s), and Standard Operation Procedures (SOP’s)
Project Planning
Clinical Plan Development
Site Identification and Assessment
Regulatory Affairs
Coordination of Investigational Sites
Clinical Monitoring
Medical Monitoring
Quality Assurance
Management of drug and laboratory samples
Registration of new products / indications
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COLOMBIA HEADQUARTERS
Cr 37a # 8 - 43, Edif. Rose Street Ofic. 901,
Medellin,
Colombia,
050010
