Igniting Innovation Through Deep Empathy
[WEBINAR] State of the Industry Webinar: U.S. Regulatory Policy Improvements
FDA 483 Responses: Avoiding Common Pitfalls and Deficiencies (Ep. 8 on The Pharmcast)
This week on The Pharmcast, we explore best practices and common pitfalls in FDA 483 Responses. In 2015, there were an average of 175 inspections and 10 warning letters issued per...
[WEBINAR] Knowledge Management: How to Capture, Retain, & Leverage Expertise Before It Walks Out the Door
FSMA Implementation: Getting Past “What” to “How”
After five years of listening sessions, draft rules, comment periods, discussion, analysis, planning, and compromising, the rules are final and the first compliance date for the Food...
FSMA Implementation: 3 Lessons Learned Along the Way
Over the course of my 36 years with The Hershey Company, I helped lead and execute a number of global Quality, Regulatory, and Governance initiatives. Perhaps one of the most...
FSMA Compliance: 4 Steps to Move Forward with Confidence
The time is now, yet the journey is still just beginning. Since January 2011, significant work has been underway by both food regulators and the regulated industries preparing for...
Real World Evidence: Times They Are a (Slowly) Changin'
Per the FDA’s PDUFA VI "commitment letter," the agency will face some real world deadlines to advance the use of real world evidence. But, since we’re dealing with the real world, let’s...
[WEBINAR] Keys to Breakthrough Margin Improvement
In this session Dr. Dahlgren and Dr. Kamman will share Keys to Breakthrough Margin Improvement. Gleaned from over 60 years of combined experience in R&D and Quality for leading CPG and Food companies,
Dr. Joseph Lamendola Fails Retirement: Joins YourEncore as SVP of Regulatory Practice
YourEncore is pleased to announce that Dr. Joseph Lamendola has failed retirement and joined YourEncore on a full-time basis to be Senior Vice President of its Regulatory Practice. “Dr. Lamendola...
YourEncore at DIA 2015