Welcome to our new website! If this is the first time you are logging in on the new site, you will need to reset your password. Please contact us at email@example.com if you need assistance.
Your membership opens the door to free learning resources on demand. Check out the Member Knowledge Center for free webcasts, publications and online courses.
Our new book is a comprehensive look at a vital part of medicines development and regulatory affairs. Grab your copy today!
Hear from leaders around the globe as they share insights about their experiences and lessons learned throughout their certification journey.
Up until mid-March 2020, regulatory professionals were traveling globally, attending meetings with regulatory agencies, planning for FDA Advisory Committees and CHMP Oral Explanations and attending conferences. where regulators would turn up to offer their current thoughts on various aspects of drug development. Now we are all working virtually, wondering how society might change as a result of COVID-19. This webcast will not try to predict how the geopolitical world will change as a consequence of COVID-19, but will cover current hot topics and emerging challenges affecting regulatory affairs professionals globally. Questions to be discussed include:
We may not have all the answers, but we hope to help you apply additional creative thinking as you navigate the uncertainty of the current regulatory environment.
Intermediate: Content is designed based upon the assumption that individuals have basic knowledge of the topic(s) and/or demonstrated competence related to the topic(s). Higher-level concepts are introduced during lectures; exercises requiring synthesis and/or application of concepts are incorporated into the activity.
Who Should Attend
Over a 30-year regulatory career, Joe has been responsible for 30+ approvals across 10+ therapeutic areas. With hundreds, if not thousands, of agency interactions under his belt, Joe provides clients with the insights, relationships, and credibility needed to bring drugs to patients quicker. Beyond drug development, Joe is an expert in strategic alliance governance and organization design, having developed the first BMS US regulatory organization.
Prior to joining YourEncore, Joe served as the US VP of Regulatory Sciences for Bristol Myers Squibb and VP of Regulatory Affairs with US and global experience for Schering Plough. In this role, Joe was responsible for leading the regulatory strategy for all global programs across the preclinical, clinical and approval stages.
Joe believes his ability to collaborate across matrixed organizations and maintain a sense of humor throughout the thrills and challenges of drug development have largely contributed to his success.
Graham Higson has over 35 years of experience in the pharmaceutical industry. Since 2014, he has worked as a Regulatory consultant specializing in the provision of strategic regulatory advice, drug development, regulatory outsourcing and organizational development. Prior to his shift to consulting, he was Managing Director of NDA Advisory Services where he was accountable for the organization’s Regulatory and HTA Advisory Boards.
Early in his career, Graham was the Global Head of Regulatory Affairs for the medical diagnostics division of GE Healthcare and he spent five years at AstraZeneca as Vice President and Global Head of Global Regulatory Affairs, where he led the regulatory organisations across six R&D sites in the UK, Sweden, US and Japan. He held a number of senior regulatory positions in the UK and USA during his 11 year tenure at Pfizer, and he has also worked at Gensia, Sandoz, Ciba-Geigy, Synthѐlabo and Baxter Healthcare.
Graham has served on the EFPIA and PhRMA regulatory affairs committees, the CMR Regulations Advisory Board and the TOPRA Regulatory Advisory Council. He is also a member of the NDA Regulatory Advisory Board, comprised of former senior European regulators and industry experts.
Steve Pondell is a CMC expert in the manufacturing, compliance and regulatory aspects of product development from clinical manufacturing, through global regulatory approvals and into commercial production. He has experience working with small biotech companies as well as multi-national pharmaceutical companies, and has served as a contract manufacturer and as a virtual manufacturing outsourcing manager. His specialty is assisting companies work across the sponsor/contract manufacturing relationship, creating high performing partnerships on a global basis.
Steve presently serves as a Managing Expert, Regulatory Center of Excellence at YourEncore. As an expert consultant, Steve has helped a variety of small to medium sized pharma and biotech companies with projects that include GMP Gap Analyses, product development programs, CMC regulatory dossiers, cGMP compliance and supplier audits, and business development activities for a global logistics provider.