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Investigator Initiated Research Agreement (US)
Foley & Lardner LLP

This is a sample template for an investigator initiated research agreement.

Resource Details
Interest Area: Health Law
Source: Resource Library
Region: United States
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Considerations When Responding to a Document Subpoena (US)
Foley & Lardner LLP

This checklist includes the considerations when responding to a document subpoena.

Resource Details
Interest Area: Compliance and Ethics, Government, Health Law
Source: Resource Library
Region: United States
Audience: New to In-House, Small Law Departments, Large Law Departments
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Compliance Effectiveness Review - HIPPA Security Checklist (US)
Foley & Lardner LLP

This checklist is for the health law industry members to evaluate HIPPA security compliance effectiveness.

Resource Details
Interest Area: Compliance and Ethics, Health Law, Technology, Privacy, and eCommerce
Source: Resource Library
Region: United States
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Whether it’s plaintiff’s attorneys or the federal or state government, the healthcare industry is under constant scrutiny and attack. Join experienced in-house and outside healthcare counsel explain the current trends, what might be looming on the horizon, and what you should do if an investigator knocks on your door.

This resource discusses the regulation of patented medicines (this resource is in French).

This resource discusses how to best protect confidential information, such as trade secrets, personally identifiable information and company proprietary information. The resource further discusses the relevant laws, such as Sarbanes-Oxley and HIPAA.

This resource discusses the Patented Medicine Prices Review Board (PMBRD), including its origin and mandate, as well as the price regulatory framework, the price review process, and the review of excessive price guidelines.

Whether it’s plaintiff’s attorneys or the federal or state government, the healthcare industry is under constant scrutiny and attack. Join experienced in-house and outside healthcare counsel explain the current trends, what might be looming on the horizon, and what you should do if an investigator knocks on your door.

This resource explains healthcare product advertising and drug promotion in Canada. In addition, this document describes the relevant codes and laws, including Health Canada and PAAB.

<br />This program will provide guidance regarding your ethical obligation for responding to government requests for information, including informal letters from government agencies or their contractors, OIG subpoenas, HIPAA subpoenas, civil and administrative investigative demands, congressional and grand jury subpoenas. Various other ethical issues, including privilege, will also be addressed.

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