Clinical Trial Training Series

With the push for improved compliance and enforcement — and a legion of newly-hired and -trained investigators — the FDA is coming down hard on sponsors and sites to comply with Good Clinical Practices (GCP).

But with limited budgets, training directors are having a hard time finding cost effective training tools to educate their staff.

Sending employees for training off-site can be time-consuming and expensive. And it can be frustrating when an employee you’ve trained leaves you to go to work for a competitor — and you’re forced to start all over again.

But there is an easier way. Now you can train staff yourself — for significantly less money — in your own office, on your own schedule.

For years, GCP compliance and training directors have asked FDAnews for help with their training needs.  And now we’ve come up with an unbeatable solution.

We’ve pulled the “best of” our webinar and virtual conference recordings and packaged them together for one low price.  With nearly 15 hours of content, the Clinical Trials On-Demand Training Series is a cost-effective way to give your staff the kind of high-level education they want and need … with the flexibility that makes in-house training most beneficial.

With it, you can train your entire staff … or one person at a time … at their own pace … at a time that’s convenient … as an all-day crash course, or an hour or two at a time to view just one section.

And, if you or staff members need a brush-up, you can easily go back and select the sections you need to review.

The FDAnews Clinical Trials On-Demand Training Series is your best option to keep your training current  — without blowing your budget.

Here’s how it works: To provide you with the most up-to-date training possible, the Training Series is available as a one-year subscription. You’ll have immediate online access to nearly 15 hours of recordings from our clinical trials vault, and, throughout your subscription term, new recordings of select FDAnews webinars and virtual conferences will be made available to you — for no additional charge.

There’s no better time to subscribe than now. With this introductory offer, you pay just $897, a $400 savings off the regular full price of $1,297. Staff training has never before been this affordable. Please read on for more information.

The Clinical Trials On-Demand Training Series puts you fully in control of your training, and lets you avoid the stress of having to plan your daily work around off-site training. It allows you to plan sessions at times that work best for your company, that are convenient to you and your staff, and for an amount of time that fits your company’s day-to-day business schedule.

But most importantly, the Clinical Trials On-Demand Training Series gives you the effective top-level training you need, while keeping its cost at a minimum. At last, you can solve your training problems the easy way — and greet FDA investigators with confidence.

The Sessions:

  • Managing Clinical Investigators in 2010 and Beyond — FDA’s Final Guidance for Investigator Responsibilities
  • Risk Strategies in Clinical Trial Contracts — How to Write Win-Win Indemnification Clauses
  • Clinical Trial Inspections — What a Former FDA Official Can Tell You About Noncompliance
  • Case Study:  Conducting EU Studies from a US Virtual Biotech Company
  • Protection and Transfer of Clinical Trial and Adverse Event Data within the Patchwork of EU Regulations
  • Avoid Clinical Trial Liability Lawsuits — Improving Your Informed Consent Practices
  • Clinical Trial Billing Under Medicare — Overcome Billing Irregularities to Avoid Regulatory Challenges
  • Falsified Data in Clinical Trials — How to Determine What to Report to the FDA
  • Understanding Clinical Trial Regulations in Austria, Germany, Hungary, Poland
  • Securing Insurance for Running Trials in EU Countries
  • Managing Postmarket and Pharmacovigilance Related Trials in the EU
  • Results of the “Road Map Initiative for Clinical Research in Europe” Workshops — Where Does the Road Lead Us?

Users include:

  • Clinical quality assurance managers and auditors
  • Clinical site directors
  • Clinical research associates/coordinators
  • Regulatory affairs
  • IRB administrators
  • GCP training staff

Companies who will benefit include:

  • Drug companies
  • Biotech companies
  • Device companies
  • Diagnostic companies
  • CROs
  • Academic and public/private research facilities
  • Institutional review boards

Regularly $1,297 for a site-wide license. But order TODAY and you save $400. Your price: just $897. Act now: place your order today. Multi-site and global pricing available on request. Please contact customer service at or call toll free (888) 838-5578 (inside the U.S.) or +1 (703) 538-7600.