Patrick P. Den Boer

About Patrick P. Den Boer

Patrick P. Den Boer serves as the Chief Executive Officer of QPharma, where he directs the strategic management of the company.Pat is a recognized expert in the Pharmaceutical Industry, in areas such as Computer System Validation, PDMA Compliance, Sample Accountability, Sales Force Automation, Warehousing, Fulfillment, and Pharmacy operations. He founded the Professional Services division of QPharma in 1994, where he served as President for 10 years. Pat built the organization from a small start up IT services company to a global multi-million dollar regulatory compliance solutions firm. The PDMA Services division was formed in June to assist pharmaceutical companies in complying with the Prescription Drug Marketing Act. In 2006, the Fulfillment and Pharmacy Services division was created as a natural extension for QPharma to ship prescription drug requests to Practitioners, Sales Representatives, and Patients. Prior to founding QPharma, Pat served as Validation Manager at Warner Lambert (now Pfizer) and Anaquest (now a division of Baxter). He also served in various positions at Lederle Laboratories early in his career. Pat is a 1985 graduate of Steven\'s Institute of Technology where he received his B.S. in Chemical Biology. He received his M.S. in Software Engineering from Iona College in 1988.Specialties: General Business Management, Strategic Planning, Mergers and Acquisition and Strategic Planning

Experience

1. President & CEO

   QPharma, Inc.

   Jun 1994 — Present · Morristown, NJ, US

   I am responsible for defining and managing the strategic goals of the company as well as managing and developing staff to achieve the strategic goals of the organization. I am involved in all facets of the organization, including proposal development and negotiations, risk management, corporate policy, project and corporate presentations, human resources and budget management.

Education

• Stevens Institute of Technology

  BS, Chemical Biology

  1980 — 1985

• Iona University

  MS, Software Engineering

  1988 — 1989

Skills

• Pdma
• Validation
• Strategic Planning
• 21 Cfr Part 11
• Thought Leadership
• Iso 13485
• Biotechnology
• Business Strategy
• Computer System Validation
• Change Control
• Regulatory Affairs
• Lifesciences
• Pharmacovigilance
• Gmp
• Compliance
• Iso
• Pharmaceutical Industry
• Sop
• Fda
• Product Development
• Technology Transfer
• Start-Ups
• P&L Responsibility
• Data Management
• Quality Management
• Gamp
• Cross-Functional Team Leadership
• Marketing
• Healthcare
• Process Improvement
• Quality System
• V&V
• Document Management
• Process Simulation
• Quality Assurance
• Mergers & Acquisitions
• Commercialization
• Software Documentation
• Gxp
• Quality Auditing