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About

About the services

Sanity Consulting provides portfolio and program management and business process design solutions for the biotechnology, medical devices, life sciences, and diagnostics industries. Technical writing services are also available for individual documents or as part of larger projects.

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Why should you choose Sanity Consulting

You work with complex systems, subject to external regulatory and market constraints, in an environment of constant change and ambiguity. Your teams need order and organization, while retaining adaptability and avoiding bureaucracy. With Sanity Consulting you get:

  • Less chaos and ambiguity; improved efficiency in your programs and processes
  • Customized solutions for what your teams need, without over-complication
  • One-on-one support from a highly experienced program manager accustomed to working in complex, fast-paced environments
  • Transparent communication: Clearly defined scope and schedule of work, regular updates on progress, and timely notifications of risks and delays
  • See Use Cases for examples of how Sanity Consulting can help your teams

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About the owner

My name is Saniya Fayzullina. As the sole owner of Sanity Consulting, I will work with you to understand your company’s needs and fully customize the services I deliver. My guiding principle is that solutions should be fit for purpose: following common sense and avoiding over-engineering. I emphasize easy-to-use tools, clearly defined processes, and consistent unambiguous communication. In addition to program and portfolio management certifications, I also hold a PhD in Pathobiology and have extensive experience working with bench scientists, bioinformatics scientists, and software engineers. I excel at bringing together development and regulatory, quality, and operations teams to achieve business objectives.

I’m based in the San Francisco Bay Area. I’m available in person/on site in the Bay Area and remotely for other locations. 


Summary of experience and qualifications:

  • Program and portfolio management and business process design experience in the medical devices industry
  • 510k, PMA, IDE, and CE mark (IVDD and IVDR) filings
  • Design Quality and Risk Management under Design Controls
  • Portfolio Management Professional certification (PfMP) from PMI
  • Project Management Professional certification (PMP) from PMI
  • Regulatory Affairs Certificate: Medical Devices from RAPS
  • PhD in Pathobiology from Johns Hopkins School of Medicine
  • Mediation and Conflict Resolution Certificate from UC Berkeley
  • Technical writing: academic publications, regulatory submissions, internal procedures, design and development documentation
  • Comfortable working in a variety of enterprise software: Jira, Google Suite, Microsoft Office Suite, Smartsheets, Adobe Acrobat Pro, Veeva eQMS, AODocs eQMS, Matrix Requirements eQMS

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