ERP Horror Stories: How a Manufacturer Failed an FDA Audit and Lost $600M in Valuation in a Day

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Manufacturers in regulated industries face stringent regulations, with compliance often being a matter of significant consequence. These regulations are not just bureaucratic hurdles; they're designed to ensure safety, quality, and trustworthiness in the products delivered to consumers.

Failing to adhere can result in severe financial penalties, reputational damage, and even legal ramifications, emphasizing the critical need for manufacturers to be both informed and diligent in their industry practices.

In the most recent "ERP Horror Story," Microsoft Partners HSO and Merit Solutions talk about a manufacturer's ERP setup that wasn’t properly tailored to their specific industry. The company faced a flawed FDA audit, resulting in a staggering $600 million loss in valuation and a 40% decline in stock price overnight.

WATCH ON-DEMAND NOW: ERP Horror Stories: How a Manufacturer Failed an FDA Audit and Lost $600M in Valuation in a Day

Key highlights of the discussion will include:

  • How to use your ERP as a way to safeguard your company’s future, regardless of your industry's compliance demands with the FDA, ISO, or others.
  • Tips for selecting the right partner for your D365 deployment or upgrade.
  • Understanding why a generic version of D365 might not meet your needs.
  • The scary consequences of neglecting digital infrastructure.
  • How to avoid costly technological missteps that could severely impact your company.

Presenters:

Rick Harper, Area Executive, Regulated Industries, HSO

Bill Burke, CEO, Merit Solutions

Moderator:

Anya Ciecierski, Co-Founder, ERP/CRM Software Blog

ERP Horror Stories: ERP Horror Stories: How a Manufacturer Failed an FDA Audit and Lost $600M in Valuation in a Day

WATCH ON-DEMAND NOW: ERP Horror Stories: How a Manufacturer Failed an FDA Audit and Lost $600M in Valuation in a Day

By ERP Software Blog Writers, www.erpsoftwareblog.com

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