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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 h...
Strategic Planning in Clinical Trials and Drug Supply
Jason Nolte, Clinical subject matter expert, discusses the importance of strategic planning teams and what they must utilize to stay relevant in the Clinical Trial & Drug Supply industry.
Bioethics: Application and Implementation
In this Expert Q&A session, Luann Van Campen, Ph.D., M.A., and Don Therasse, M.D., provide valuable insights into the implementation of bioethics best practices within life sciences organizations.
Audits: A Brave New World, Time for a Refresh?
Written by Jane Wood, this is an abbreviated version of an article in The RQA Magazine about the rapidly evolving world of clinical trials and the technology and data that rule within them.
Good Laboratory Practices - The Importance of Preparation and Execution
Deb Sedor, former Director of Quality Assurance at J&J, and Managing Expert for YourEncore’s Quality CoE, discusses the importance of preparation and execution when it comes to Good Lab Practices.
Compliance, Clinical Operations, or Quality: What Team Do You Play For?
Some pharma professionals need a gentle reminder that they are, in fact, on the same team – driving toward the same goals. Read more from Arti Bajpai about quality and compliance in a team setting.
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.
Data Integrity - It's All About the Data!
Jane Wood, Principal of YourEncore's Quality Center of Excellence, discusses the importance of Data Integrity in any Quality system.
Clinical Regulatory Inspections – and why I love them
Jane Wood, Principal of YourEncore's Quality Center of Excellence, discusses the importance behind clinical regulatory inspection readiness.
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