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White Paper Vanesa Vasadi Figueroa

White Paper: Environmental Monitoring in cleanrooms. Six factors to consider when evaluating a digital system

We are honored to present this interesting White Paper in which Vanesa Vasadi Figueroa reviews six key factors for the decision process of selecting software for an Environmental Monitoring (EM) program. She explains how each of those factors can improve workflow efficiency and overall compliance, facilitate the detection of potential contamination or adverse trends, and ultimately lean into a more data-driven culture.

The first two considerations review the core requirements one should look for when evaluating and considering a digital system for purchase:

  • Ensuring fundamental compliance with regulations.
  • Meeting best practices for software validation.
  • Ease of implementation.

The paper then discusses the user experience related to everyday interaction with the system and how an intuitive workflow can improve functionality and usability, ultimately; reduce the burden on scientists. Lastly, she discusses data management, interpretation, and frequent, reliable reporting for investigations and trends.

Vanessa Vasadi Figueroa, Chief Executive Microbiologist and Independent Consultant at VVF Science®, has more than 17 years of combined experience in the life sciences industry, supporting Pharmaceutical, Biotechnology and Medical Device companies. Mrs Figueroa’s core expertise is in sterility assurance, contamination control, microbial investigations, and environmental utilities.

Learn more about environmental monitoring by downloading the poster: Expecting more from your EM software, created by our product manager, Enric Adserà in collaboration with Vanessa Figueroa.

Vanessa Figueroa leverages her combined knowledge of the Pharmaceutical, Biotechnology and Medical Decives industries to provide manufacturers across the US, Europe and India with critical laboratory operations management and personnel training programs to ensure compliance with cGMPs as well as global regulatory standards.

Combining hands-on Quality Control, Sterility, Inspection, and Compliant Operations with an educational leadership approach and natural business acumen, Vanessa brings 17+ years of real-time experience to deliver transformational real-world results.


Vanessa Figueroa leverages her combined knowledge of the Pharmaceutical, Biotechnology and Medical Decives industries to provide manufacturers across the US, Europe and India with critical laboratory operations management and personnel training programs to ensure compliance with cGMPs as well as global regulatory standards.

Combining hands-on Quality Control, Sterility, Inspection, and Compliant Operations with an educational leadership approach and natural business acumen, Vanessa brings 17+ years of real-time experience to deliver transformational real-world results.

Vanessa Figueroa leverages her combined knowledge of the Pharmaceutical, Biotechnology and Medical Decives industries to provide manufacturers across the US, Europe and India with critical laboratory operations management and personnel training programs to ensure compliance with cGMPs as well as global regulatory standards.

Combining hands-on Quality Control, Sterility, Inspection, and Compliant Operations with an educational leadership approach and natural business acumen, Vanessa brings 17+ years of real-time experience to deliver transformational real-world results.

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