Webinar Information

MORE INFO: http://www.feith.com/webinar-bpm-for-pharmaceuticals

QUESTIONS: Please direct all inquiries to: [email protected]

What You'll Learn

What are your biggest barriers to achieving your Pharmacovigilance goals? Many pharmaceutical, bio, and medical device companies and CROs are struggling to manage changing and challenging mandated Risk Evaluation & Mitigation Strategy and Risk-Management Plan obligations. How do we maintain compliance and reduce our risk while operating in a more efficient, more accurate, and more cost-effective environment? And how do we correctly manage Global Operations with centralized communications and keep everyone instantly on the same changing page?

Utilizing manual REMS & RMP Tracking processes with antiquated tools is inadequate and results in poor process visibility and increased compliance risk. These are just a few of the struggles Pharmacovigilance professionals like you are dealing with when managing PV plans on a global basis. But fret not because there is hope: By leveraging efficient, streamlined Business Process Management technology and best practices, achieving your RMP Tracking goals is possible, with solutions including:

• Centralized RMP tracking tools
• Standardized RMP information repositories
• Monitoring RMP status and obligations with a single portal
• Meeting changing HA requirements quickly and more adaptably
• Increased coordination with PV Group activities
• Increased oversight for mitigating compliance risk
• Harmonized reporting for QPPV review
• Compliance for Inspection Rediness
• And much more

Join your hosts for this exclusive session on solving your stickiest challenges in the Drug & Medical Device regulatory landscape, automating Risk Management Plan obligations, addressing global PV/DS Group operational issues, and how to evaluate agile BPM platform technologies and how Business Process Management can ease your operation frustration such as:

• Complex and disorganized tracking due to the sheer volume of RM Activities globally
• Managing RMPs completely through versioning, submission, and roll-out
• PV surveillance and reporting while requirements are in flux
• PV routine and additional activities that vary in frequency and duration
• Lack of a unified tool for tracking plan activities, investigations, and milestones
• Lack of visibility into status of RMP obligations

What You'll See

Find out how you can benefit from streamlining your pharmaceutical business processes by automating capture, routing, notification, and approval with one unified interface by reducing processing costs, decreasing manual effort, increasing accuracy, improving timeliness, and eliminating lost items in:

• Pharmacovigilance
• Adverse Event Tracking
• Patient Risk Management Plan Tracking
• Records Management
• Internal and External Reporting
• Inventory Tracking
• Back-office Operations such as Human Resources, Travel & Expense, and Accounting
• Manufacturing Solutions such as Engineering Document Management and Material Safety Data Sheet Management
• And much more.