Versions Compared

Key

  • This line was added.
  • This line was removed.
  • Formatting was changed.

...

Demonstrating Real-World Impact of Modernization of Statistical Analytics (MSA) Framework

Project Scope:

The PHUSE project team will extend the MSA framework by creating a reference architecture that takes into account real-world scenarios and design solutions to remediate them, ultimately providing a practical guide to building an end-to-end validated environment for regulated work. Companies seeking to build an open-source programming environment for regulatory reporting can leverage the MSA framework for guidance.

However, since the framework is designed to be both flexible and extensible, implementing it may prove challenging for companies, resulting in situations where risks are not sufficiently mitigated. While the original MSA paper provided conceptual guidance, the PHUSE handover of the project will seek to provide an overview of practical implementations of the framework being applied.

Current Status:

  • Finish business case/technical implementation review.​

  • Aggregate primary business case/technical implementation points and map with MSA tenets.​

  • Choose most relevant technical implementation options.​

  • Begin testing implementation options with examples.

  • Finish business case/technical implementation review.​

  • Aggregate primary business case/technical implementation points and map with MSA tenets.​

  • Choose most relevant technical implementation options.​

  • Begin testing implementation options with examples.

Regular Project Meeting Day/Time:

  • Bi-weekly: Wednesdays 14:00-15:00 BST

Key Skills:

  • Experience with the MSA Framework.

Communication of Version Metadata for Open-Source Languages

Project Scope:

This project aims to develop a new template or enhance an existing one such as the Study Data Standardization Plan (SDSP) or Analysis Data Reviewer’s Guide (ADRG), to ensure that metadata pertaining to the versions of statistical packages and procedures is consistently documented in alignment with health authority expectations. This standardized template will streamline the submission of clinical study metadata to health authorities as part of the regulatory review process.

Current Status:

  • Create ADRG R package​

  • Create ADRG:

  • Completion​ guideline for OS​

  • ADRG OS example

    Regular Project Meeting Day/Time:

    • Monthly: Wednesdays 19:00-20:00 BST

    Key Skills:

    • Experience with the Study Data Standardization Plan (SDSP)

    • Experience with the Analysis Data Reviewer’s Guide (ADRG)