Pharmaceutical and life science companies face tremendous challenges due to constantly changing industry demands. Macro challenges, such as new government regulations, health insurance company policies, and the introduction of generic drugs have
resulted in increased price pressure for pharmaceutical companies. These challenges coupled with micro challenges, such as the necessity for constant research and development, active marketing efforts, and increased business complexity in emerging
markets have resulted in diminishing margins. Pharmaceutical companies are constantly challenged to increase revenues and improve operational efficiency throughout their organizations. They struggle to adopt shorter new drug development cycles
while maintaining US and International regulatory compliance standards: a task that is highly complex, time-extensive, and costly.
iPharma360 Overview
iPharma360 : Regulatory, Operational and Collaborative Solution
iPharma360 is an enterprise wide pharmaceutical, life sciences, medical device, and product life cycle management solution that is comprised of a suite of 21
CFR and GxP compliant applications.
The Suite Includes: Document Change Control, Dossier Management, Drug Master File, Artwork Management, Marketing Communications, Quality Management, Electronic Common Technical Documentation (eCTD), Legal, Shipping and Logistics.
iPharma360 addresses the operational, regulatory and collaborative challenges that come with each stage of the existing or new drug, device or product development lifecycle.
