OARO COMPLY

Relying on clipboards and signatures is not only inefficient and expensive, it’s also inaccurate. The world has evolved and so have our methods of quality management, especially in industries such as pharmaceuticals, life sciences, and manufacturing. This enterprise grade solution establishes standards, identity deviations and analyzes quality events, improving the safety, efficacy and profitability of your organization’s products.

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Benefits

Standardized and automated quality processes to ensure regulatory compliance

Reduced legal and compliance risks arising from human error or lost reports

Accelerated adoption of technology resulting from an intuitive user experience

Automated verifications, notifications, and document reconciliation

Enforced execution of plans and standards

Customized rules for form filling, signing, and validation

Increased transparency throughout the organization

Reduced waste to meet sustainability goals

Case Application

Multinational Pharmaceutical Company

Note. Due to the confidential nature of some of our projects, we’ve omitted the client’s name. For references to further details, please contact us directly.

Reducing the administrative burden of quality assurance

About the client

  • - Revenues of more than $30B annually
  • - 100,000 employees in 150 countries

Quality assurance in the pharmaceutical industry can be onerous. Unfortunately for our client, the staggering administrative burden is both costly, inefficient, and puts a heavy strain on employees. OARO crafted a digital version of its robust quality assurance process using blockchain technology. The result was a program that saved time, money, but also offered the client greater security and transparency.

CUSTOMER REPORTED:

• 70% reduction in admin time saving over 10,000 hours

• Projected annual savings of $300K USD per manufacturing site

• Improved quality risk management

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