Posts Tagged With 'webinar'

  • Jun
  • 04
  • 2012

Please Join Us For Our Next Webinar: Ensuring Successful FDA Meetings

Please Join Us For Our Next Webinar: Ensuring Successful FDA Meetings

“Ensuring Successful FDA Meetings”
Wednesday, June 20, 2012
12 p.m. (EDT) | 9 a.m. (PDT) | 5 p.m. (GMT)

Online Registration

FDA meetings, regardless of when they occur — from pre-IND, to End-of-Phase 2, to pre-NDA meetings — can make or break your chances of bringing your product to final approval. Ensuring successful meetings is therefore a key part of your overall product development plan. Please join:

Joel Falk, EVP of Product Regulation & Compliance, and Lauren Wind, Senior Consultant, as they discuss key tactics, such as:
• Assuring your submissions provide compelling support to your goals for the meeting
• Structuring your questions to maximize unambiguous responses
• Preparing for the actual meeting — the “Tiger Team”
• Deciding whether to commit or not to commit
• How to best utilize the participants on your side of the table
As well as other methods to increase your success with the FDA.

This complimentary, one-hour webinar is designed to help life science executives understand how to maximize success when meeting with FDA regulators.

To join the webinar, please register here. Upon receipt of registration, a dial-in number and log-in information will be sent.

  • Mar
  • 19
  • 2012

Please Join Us for Our Next Webinar: “New Biosimiliars Guidance- Has Anything Changed?”

Please Join Us for Our Next Webinar: "New Biosimiliars Guidance- Has Anything Changed?"

“New Biosimilars Guidance- Has Anything Changed?”

A Webinar Presented by The Weinberg Group

Wednesday, March 28, 2012

12 p.m. (EDT) | 9 a.m. (PDT) | 5 p.m. (GMT)

Online Registration

The path to lowering the cost of health care requires innovative thinking throughout the drug development process. Important biologic medicines are soon coming to the end of their exclusive marketing periods and follow-on biologics – also called biosimilars – are poised to be introduced in greater numbers in the US. This webinar will provide insights from biologic development and lessons learned from the process that has unfolded to date, as well as the impact of the recent FDA guidance documents. Please join:

Bob Roth, Ph.D., M.D., Vice President and Worldwide Medical Director and
Nick Fleischer, Ph.D., Vice President, Clinical Pharmacology & Biopharmaceutics as they discuss

▪ The state of regulatory pathways to approval based on case experience
▪ Best practices and lessons learned in developing biosimilars
▪ A view of the future abbreviated pathway for biosimilars
▪ The recent FDA draft guidances: what is now different?
▪ The challenges associated with launching biosimilars

This complimentary, one-hour webinar is designed to help life science executives understand the market opportunity in pursuing biosimilars.

To join the webinar, please register here. Upon receipt of registration, a dial-in number and log-in information will be sent.

  • Jan
  • 23
  • 2012

Please Join Us For Our Next Webinar: “Understanding What FDA is Looking For in Postmarket Safety Assessments”

Please Join Us For Our Next Webinar: "Understanding What FDA is Looking For in Postmarket Safety Assessments"

“Understanding What FDA is Looking for in Postmarket Safety Assessments: Going Beyond AERS.”

A Webinar Presented by The Weinberg Group

Wednesday, February 8, 2012

12 p.m. (EDT) | 9 a.m. (PDT) | 5 p.m. (GMT)

Online Registration

As we know, getting a drug approved by FDA is hardly the last step. FDA’s oversight continues well past approvals and over the years, has become more vigilant regarding safety and efficacy. This greater focus means postmarket safety assessments are playing a growing and increasingly critical role within your regulatory group. During this webinar, Dr. Bob Roth will explain how to get the information FDA is looking for, and how to communicate this information, both good and bad, to FDA.

Please join Bob Roth, Ph.D., M.D. Vice President and Worldwide Medical Director, as he discusses:

- VigiBase, the international equivalent of AERS
- Drug Abuse Warning Network (DAWN)
- National Poison Data System (NPDS)
- Useful analyses and data presentations
- Application to special risk settings

This complimentary, one-hour webinar is designed to help decision makers and regulatory affairs professionals understand what FDA is looking for in post market safety assessments.

To join the webinar, please register here. Upon receipt of registration, a dial-in number and log-in information will be sent.

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