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The docs for RuleSetReferenceId are helpful, as is I believe this directory in the source tree. Basically put java in front of these files to turn on the rules there.
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Start by opening the PMD list 1 document on your computer or device.
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Fill in the top section with the relevant information, such as the date, project name, and any other required details.
03
Review the list of items or tasks that need to be addressed in the PMD. Read through each point carefully to ensure you understand what is being asked.
04
Begin filling in the document by going through each item one by one. For each item, write a brief description or explanation of what needs to be done to address it.
05
Use clear and concise language to convey your thoughts. Make sure your answers are complete and address all components of each item on the list.
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Who needs a PMD list 1 doc:

01
Project managers: PMD lists are commonly used by project managers to keep track of the tasks and responsibilities associated with a particular project. The list helps them ensure that all necessary tasks are being addressed and completed in a timely manner.
02
Team members: Team members working on a project can benefit from having access to a PMD list 1 doc. It helps to provide clarity on their individual tasks and the overall project goals, making it easier for them to prioritize and stay organized.
03
Stakeholders: Stakeholders, such as clients or sponsors, may also need a PMD list 1 doc to have visibility into the progress of a project. It allows them to understand what tasks are being worked on and when they are expected to be completed.
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PMD List 1 doc is a document that lists all potentially market-disruptive pharmaceutical and medical devices.
Manufacturers, marketers, and distributors of pharmaceuticals and medical devices are required to file PMD List 1 doc.
PMD List 1 doc can be filled out by providing detailed information about each potentially market-disruptive pharmaceutical and medical device.
The purpose of PMD List 1 doc is to regulate potentially market-disruptive products in the pharmaceutical and medical device industry.
PMD List 1 doc must report information such as product details, market potential, potential impact on existing products, and regulatory status.
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PMD MATOSSIAN rheumatology endocrinology TELE cardiology neurology subsequent specialists arthritis

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