Live Events

Risks of Property Line Construction for Design Professionals

Jun 22

This program will discuss the risks design professionals face in connection with construction projects involving closely adjoining or attached properties. It will be presented from both the legal and engineering perspective. In connection with the former perspective, the program will discuss basic theories of liability and how to defend against them and the pre-construction protections design professionals can legally take. In connection with the latter perspective, the program will discuss basic engineering solutions to common place problems and how design professionals can protect themselves from a professional angle prior to and during construction.

What You Will Learn

  • Theories of liability and defense.
  • Real world practical, professional solutions from an engineer’s perspective.
  • Pre-construction phase dos and don’ts.
  • Construction administration phase dos and don’ts.

Who Should Attend

  • Lawyers who regularly represent design professionals.
  • Claims Managers who handle construction and architect and engineer claims.
  • Design professionals.
  • Lawyers who handle construction matters.
Package Dates Price
Risks of Property Line Construction for Design Professionals - Members Package Jun 22
$150.00
Risks of Property Line Construction for Design Professionals - Non-Member Package Jun 22
$180.00

So You Want to Handle Trucking Cases? Understanding the Basics of the Federal Motor Carrier Safety Administration Rules and Regulations

Jun 27

This “Lunch and Learn” webinar is geared towards providing a core breakdown of the Federal Motor Carrier Safety Administration Rules and Regulations for attorneys new to trucking. The program will provide an easy-to-digest review of “Hours of Service” regulations, driver logs, driver qualifications, mandated drug and alcohol testing, vehicle inspection and other federal rules applicable to commercial drivers. Panelists will also discuss FMCSA recordkeeping requirements and what documents are necessary to properly evaluate and defend a trucking case.

What You Will Learn

  • “Hours of Service” regulations.
  • Driver log requirements.
  • Driver qualifications.
  • Vehicle inspection.
  • FMCSA required recordkeeping

Who Should Attend

  • Young attorneys and transportation specialists and practitioners who are new to trucking.
  • Practicing trial lawyers handling regulation heavy trucking litigation.
  • Trucking Industry representatives and claims adjusters seeking to enhance their knowledge or get a refresher on the basics.
Package Dates Price
So You Want to Handle Trucking Cases? Understanding the Basics of the Federal Motor Carrier Safety Administration Rules and Regulations - Member Package Jun 27
$150.00
So You Want to Handle Trucking Cases? Understanding the Basics of the Federal Motor Carrier Safety Administration Rules and Regulations - Non-Member Package Nov 30
$180.00

Cybersecurity and Regulatory Issues for Drugs and Medical Devices

Jul 12

Pharmaceutical and medical device manufacturers encounter constant threats and challenges. One serious threat is a breach of cybersecurity during the product life cycle and/or during postmarket management. Other challenges to industry include patient-focused drug development, labeling of biosimilars, and regulations for medical device software, among others. The FDA recently issued Guidance on Postmarket Management of Cybersecurity in Medical Devices. The FDA is also considering Guidance on other key regulatory drug and device issues. Register now for this informative webinar to learn from two top FDA regulatory lawyers who will assist you in better understanding these critical issues.

What You Will Learn

  • The application of FDA’s Guidance for Industry regarding Postmarket Management of Cybersecurity in Medical Devices
  • Regulatory issues facing drug and medical device companies in 2017
  • Possible additional areas of consideration for future FDA Guidance for Industry

Who Should Attend

  • Practicing attorneys who regularly represent pharmaceutical and medical device companies
  • In-house and outside counsel who want to broaden their knowledge of recent and proposed FDA Guidance
  • Attorneys who advise clients on FDA regulatory issues
  • Attorneys interested in cybersecurity
Package Dates Price
Cybersecurity and Regulatory Issues for Drugs and Medical Devices - Members Jul 12
$150.00
Cybersecurity and Regulatory Issues for Drugs and Medical Devices - Non-Members Jul 12
$180.00