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New Jersey based pharmaceutical and medical device companies have a great opportunity this month to gain some significant information on how to improve their compliance outcomes and reduce their costs, using Sharepoint-based quality systems.    Sharepoint has become a darling of FDA-regulated companies due to a variety of features that are built into the Sharepoint platform that improve collaboration, increase control, and reduce costs.   Sharepoint-based Quality Systems are the next logical evolution of FDA-regulated companies implementation of quality systems.

Appropriately, the event will be held at the Microsoft offices in Iselin, NJ, and will include representatives from local companies that deliver Sharepoint-based solutions, and other Microsoft solutions targeted at FDA-regulated companies.

I’ll be there also!

What you will learn:

  • The “Core Four”: How to achieve significant improvements in quality and compliance outcomes using Microsoft Sharepoint tools with key Quality System functions.
  • Insider Secrets: What your peers and competitors are doing to maintain cost effective compliance.
  • Maximum Leverage: How your existing IT/IS investments in Microsoft tools can be used to rapidly implement a robust, cost effective Quality System.

Don’t miss the chance to gain useful information that could help your company improve its compliance outcomes.

Event Details

WHEN: February 25, 2010,     12:00 to 1:30 PM

WHERE: Microsoft Office, 194 Wood Avenue South, 6th Floor, Iselin, NJ 08830

COST: $25.00 – Includes lunch and the opportunity to network with industry colleagues

RSVP: Registration closes February 24, 2010. Seating is limited to 20 people

To register, please click here:   Microsoft/Sharepoint Solutions for FDA-Regulated Companies

Filed Under: Achieving Compliance, Events / Resources, Quality Management & Assurance Tagged With: 21 CFR Part 11, quality systems, Sharepoint

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  • About Us
    • Senior Staff
    • Why Us
    • Mission And Vision
    • Clients
    • Partners
    • Career Opportunities
  • Services
    • Inspection Readiness & Enforcement
      • FDA Inspection Readiness
      • Audits & Assessments
      • FDA Enforcement Response/Remediation
    • FDA Quality Consulting
      • Quality System & Compliance Turnarounds / Restructuring
      • Training / Coaching
      • Quality & Compliance Computer-Based Systems
      • External Supply Chain Compliance
      • Part 11 & Computer Systems Validation
      • Turnkey Quality Systems
    • Quality Assurance and Engineering
      • CRPN Quality Roadmap®
      • Quality Culture Assessment
      • Product Quality Consulting
      • Operational Efficiency/Compliance Effectiveness
      • Project/Program Management
    • Corporate Compliance and Litigation
      • Corporate Compliance Programs
      • Interactions With Department Of Justice And The Courts
    • FDA Regulatory Consultants
      • Product Development / Submissions / Commercialization
      • REMS (Risk Evaluation And Mitigation Strategies)
      • Mergers / Acquisitions / Licensing
    • Quality, Compliance, Regulatory & Operations’ Staffing
      • Staffing
      • Talent Management
      • Rapid Turnaround
  • Innovative Solutions
    • Writing for Compliance®
    • CRPN Quality Roadmap®
    • Quality Pulse®
    • IEEP
    • REMS
  • Success Stories
  • Industries
    • Biopharmaceuticals
    • Cannabis/CBD
    • Cell & Gene Therapies
    • Combination Products
    • Cosmetics
    • Dietary Supplements
    • Medical Devices and Diagnostics
    • Pharmaceuticals
  • Contact Us

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