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ClinForward, Inc. provides Clinical Research consulting services to pharma, biotech companies and CROs for Phase I-IV. Pharmaceutical and biotechnology clinical trials including:. Clinical Monitoring (Qualification, Initiation, Interim and Close-out). Consent review and development. Pre-Study Site Qualification and Site Selection. Initiation training and presentations. Study Tools and Manuals. Site budget review and negotiation. CRA and site audits.
ClinfoSource: Clinical Research Education Online
Clinical Research Education Online. We offer Online Training Certificate Programs for GCP Compliance. This program consists of core and advanced topics pertaining to GCP applicable to Investigational sites. It offers necessary training in the regulations and standards governing clinical trials in human subjects for Investigators, Study Coordinators and Pharmacists. Raquo; Individual Enrollment. Raquo; Group Enrollment. Raquo; Individual Enrollment. Raquo; Group Enrollment.