industry

Risk Cloud for Pharmaceuticals

As a biotech company, you face some of the most stringent regulatory requirements in the United States and around the world. The regulatory landscape is always evolving, and you need tools to stay nimble with your compliance strategies. The LogicGate Risk Cloud's technology permits you to do just that.

LogicGate for the Pharmaceuticals Industry

01

Make Compliance Part of Your DNA

From the Food and Drug Administration (FDA) to the European Medicines Agency (EMA), numerous agencies around the world impose their own sets of regulations on pharmaceutical, health sciences, and biotech firms. The LogicGate Risk Cloud helps you put the processes in place to remain compliant, such as field force monitoring and biosecurity assessments.

 

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Make Compliance Part of Your DNA
Set the Global Standard

02

Set the Global Standard

In addition to governmental laws, numerous industry best practices govern drug development and manufacturing, such as CGMP and ISO standards. Risk Cloud offers solutions that help ensure these best practices are followed through agile controls management.

 

Why Customers Choose LogicGate 

03

Manage Change Before It Manages You

Given the ever-evolving landscape of medicine, change management is a required component of any proactive governance, risk, and compliance program. Risk Cloud's automated platform assists with the effective identification, management, and implementation of necessary changes, keeping your organization prepared for what's next.

 

Reporting with LogicGate

Manage Change Before It Manages You
  • "The best part about LogicGate is the flexibility it provides fast-paced organizations to implement new processes and adapt as the company continues to change and grow. With LogicGate, we have been able to streamline our risk assessment process and equip business owners with the information they need to assess and mitigate risks on their own."

    - Head of Risk and Compliance, Healthcare

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