Home » Biopharmaceutical/Biotech » [WEBINAR] Medical Device Lunch Briefing: FDA 483 Response Best Practices
Strengthening R&D Effectiveness from the Start: The Power of the Problem Statement
“A problem well stated is a problem half solved”-Charles Kettering, former CTO of General Moto...
Quality Best Practices From an IT Perspective
Tony Ettwein, Managing Expert of YourEncore's Quality Center of Excellence, provides valuable insights into audits in IT and the different AI systems that will soon affect the Quality landscape.
State of the Industry: The Evolution of Quality and its Upcoming Challenges
Jane Wood, former Head of R&D Quality at J&J, and Principal of YourEncore’s Quality Center of Excellence discuss the current state of Quality and the future of regulation adaptation.
The Path to Patient Centricity: Part IV
Learn more from Regina Shanklin on how maximizing engagement with your audience and patients will help increase the relevance of your brand communications
The Path to Patient Centricity: Part III
Learn more from Regina Shanklin on how being useful to your audience and patients will help increase the relevance of your brand communications
The Path to Patient Centricity: Part II
Learn more from Regina Shanklin on how being completely understandable to your audience will help increase the relevance of your brand communications
The Path to Patient Centricity: Part I
Learn more from Regina Shanklin on how seeing things from the patient’s point-of-view will help you meet them where they are and increase the relevance of your brand communications
How Smart Biotechs Scale Organizations Fast and Maximize Value
Managing the Talent Roller Coaster with Virtual Development Models
Raphael G. Ognar discusses the overlying challenges biopharma organizations have and how Virtual Development can save the day.
Embracing the Virtual Development Model in Biopharma
Joseph Lamendola, PhD discusses the challenges many biopharma companies face and how Virtual Development can help create solutions.
[WEBINAR] Leveraging Evolving Regulatory Landscape to Accelerate Drug & Device Development
The Power of Community in the Era of Human Clouds: New Partnership Merges Expert Talent with California Life Science Community
Tapping Alumni for Interim Leadership
How one company got the work done while searching for the right long-term leader Minnie Baylor-Henry is an accomplished pharmacist, attorney, and regulatory affairs professional with...
[WEBINAR] Unlocking Potential: Leveraging Blockchain in the Medical Devices Industry
YourEncore experts Minnie Baylor-Henry, Darryl Glover, Donna Godward, and Vic Chance discuss the promise of Blockchain to address key issues within the Medical Devices industry.
Launching a New Business, Post-Retirement: Q&A with YourEncore Expert John Carpenter, SHRM-SCP
In an effort to expand our thought leadership, highlight Experts, and engage our Expert Community, we collaborated with YourEncore Expert, John Carpenter, to participate in our Q&A...
YourEncore Regulatory R.A.N.T. – Relevant Assessments, New Trend (2016) [WHITE PAPER]
Executive Briefing: EU Medical Device Regulation | 5 Ways EU MDR Will Impact Your Business [WHITE PAPER]
[WEBINAR] Drug-Device/Diagnostics Combination Products: Understanding the Rapidly Changing Landscape
Finding the Right Fit: Q&A with YourEncore Expert Marcia Ellett
In an effort to expand our thought leadership, highlight Experts, and engage our Expert Community, we reached out to YourEncore Expert, Marcia Ellett, to help pilot a Q&A series as a...
Executive Briefing: EU Medical Device Regulation | 5 Ways EU MDR Will Impact Your Business [White Paper]
The European Union has agreed on a new Medical Device Regulation meant to improve patient safety and data transparency. The regulation is extensive and impactful – it touches many...
Medtech Valuation Killers: 10 Regulatory & Commercialization Traps to Avoid (Ep. 11 on The Pharmcast)