Clinical Trial Management

The SMOconnect clinical operations team comprises qualified and trained people with extensive experience in managing phase I to IV studies for regulated markets.

Our SOPs are well aligned with both regulatory norms as well as best practices of the industry. SMOconnect utilizes a streamlined project management model, providing a single point of contact to oversee the people, processes, and operations.

We are committed to meeting the client’s needs for quality, compliance, and agreed-upon delivery times in order to achieve and, where possible, exceed the target plan with the guarantee that all work is carried out in accordance with SOPs, GCP/ICH guidelines and applicable regulatory requirements.

Protocol DevelopmentProject ManagementRegulatory ServicesSite Evaluation and SelectionCentral Lab ServicesClinical Trial Supply ManagementSite InitiationSite MonitoringMedical MonitoringQuality AssuranceMedical WritingStatistical Analysis