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Mastering external and cross-functional document reviews in medical writing and regulatory affairs
Enhance your collaboration with external and cross-functional stakeholders with this masterclass for medical writing and regulatory affairs professionals.
How do you review a document efficiently when your collaborators are spread across the globe and time zones? How do you ensure the confidentiality of documents while enabling everyone to work together seamlessly?
In an era of increasingly complex regulations and stakeholder collaborations, the efficiency of document reviews can make or break a project. Many organizations rely on manual, decentralized tools such as Excel and Outlook to navigate the intricate drug and medical device development landscape. Without scrutinizing and improving on the pitfalls and obstacles these manual processes bring, time and money are both wasted, pushing back projects and speed-to-market.
Join our insightful webinar “Mastering external and cross-functional document reviews in medical writing and regulatory affairs” and discover the secrets to streamlined and secure document reviews, no matter the department or geography.
Date and time: 30 January 3pm GMT
This webinar is hosted by James Wilding, VP of collaboration solutions at Ideagen and will have a special contribution from medical writing expert Diahann Homer, former Director of Oncology Medical Writing at GSK.
As VP of collaboration solutions at Ideagen, James supports organizations across the Life Sciences industry to radically overhaul their document review processes, empowering them to reach the document completion stage in significantly less time. All while improving their regulatory compliance and audit readiness.
Having worked closely with top global pharmaceuticals, CROs and medical device companies throughout his career, James has a wealth of experience to draw upon when it comes to pioneering change and raising industry standards. He is passionate about helping teams of all sizes to remove common barriers, minimize costly errors and improve document quality, so that organizations can focus on delivering critical therapies to market, faster.