Glenwood Clinical Monitoring, Inc. specializes in performing and coordinating all aspects of the clinical monitoring process from Phase I to Phase IV. Extensive experience with SAD/MAD dose-escalation studies with PK/PD/PG procedures. The company provides timely, cost-efficient, and accurate monitoring services to assess the safety and efficacy of investigational trials. Services include conducting site visits to determine site selection, protocol and regulatory compliance, file reviews, performing investigational product accountability, preparing pre/post site visit required documentation, data query resolution, reviewing AE / SAE reporting documentation, and helping clients meet critical study timelines. The company and our strategic affiliates emphasize a dedicated and personalized approach to clients and their affiliates. Additional services include Project Management, Investigator Assistance, Business Development Assistance, Training, and Auditing. Please see www.glenwoodclinical.com for additional details.