Hovsep Kirikian, Director of Product Management, USDM Life Sciences to Speak at The Knowledge Group’s Biotech & Pharma Webcast

Top Quote The Knowledge Group, the leading producer of regulatory focused webcasts, has announced today that Hovsep Kirikian, Director of Product Management, USDM Life Sciences will speak at its webcast entitled, “IT Strategies for Early-Stage Biotech & Pharma.” End Quote
  • (1888PressRelease) August 25, 2022 - This event is scheduled for September 22, 2022 from 12:00 PM to 1:30 PM (ET).

    For further details, please visit:
    https://knowledgewebcasts.com/know-portfolio/biotech-biopharma-organizations/

    About Hovsep Kirikian
    Hovsep leads USDM’s Veeva practice and has over 15 years of experience managing projects in the life sciences industry, specifically focusing on regulatory compliance, validation, equipment lifecycle, laboratory operations, and data and content management across all phases of the product life cycle.

    About USDM Life Sciences
    At USDM Life Sciences, our purpose is to bring clarity and action to the interplay of technology and regulations to help biotech, pharma, and medical device companies deliver trailblazing outcomes. We help our customers utilize cutting-edge technology to increase their speed to market while ensuring continuous compliance and patient safety. The world’s leading technology companies trust USDM to ensure their technology is adopted effectively, powerfully, and in compliance. Thousands of life science companies choose USDM to bring the future of work into the present. For more information, visit www.usdm.com.

    Event Summary:
    Early-stage life sciences organizations face many challenges, but planning and implementing IT doesn’t have to be one of them. Discover powerful tools and techniques to help you set priorities and make decisions with confidence. Follow key principles and techniques to ensure you make the right investments at the right time with partners that are the best possible fit for your organization. Learn how to build a strategic IT roadmap, define roles and responsibilities, and establish processes to make successful software investments.

    A right-sized regulatory compliance program lets you implement your GxP or SOX applications efficiently, mitigate risks to patient safety and product quality, and prepare for inspections. Achieve greater cyber maturity with privacy frameworks and safeguard privacy as your business grows in size, value, complexity, and capabilities.

    This webinar will help you to rethink your challenges and develop an IT strategy from the pre-clinical phases through commercialization.

    We will discuss:
    - Building a strategic IT roadmap that includes critical regulatory and functional requirements and milestones
    - Understanding business needs and drivers for G&A and GxP functional areas
    - Making timely and scalable IT investments
    - Establishing or harmonizing an IT compliance program to fuel growth
    - Addressing cybersecurity and privacy needs
    - Resourcing models—such as fractional CIOs, managed services, and staff augmentation—to efficiently achieve business objectives
    - Case studies for rapid growth and transformation

    About The Knowledge Group
    Founded in November 2006, The Knowledge Group has been at the forefront of providing quality continuing education programs for lawyers, accountants, financial executives, risk and compliance specialists, human resources professionals, technology officers, and business consultants in a wide range of industries.

    The Knowledge Group strives to be the best-in-class provider of continuing education by bringing forth relevant content you can’t get anywhere else.

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