26 April - 15.00-16.00 BST

Bringing novel medicinal products to market is a long, complex, and expensive process which requires drug developers to balance the need for rigorous testing with the goal of getting medicines quickly to patients who need them. To this end, both US and European regulatory agencies have developed expedited pathways to accelerate the approval process for therapies that treat serious conditions and unmet medical needs.

Veristat Regulatory experts will discuss how developers of such therapies can utilize some or multiple programs/pathways to accelerate approval in the US and Europe. This webcast will highlight the requirements, benefits, and procedures for following US pathways: Accelerated Approval, Breakthrough Therapy Designation, Fast Track, and Priority Review Designation. Then we will examine the similarities and differences to the EU pathways: Accelerated Assessment, Conditional Marketing Application (CMA), and Priority Medicines Scheme (PRIME). The discussion will culminate with real-world examples and success stories.

Learning Objectives:

• Understand when and how to apply for the following expedited pathways with FDA and European Regulatory Authorities:
  • Breakthrough Therapy
  • Fast Track
  • Priority Review
  • Accelerated Approval
  • Accelerated Assessment
  • Conditional Marketing Authorization
  • PRIME
• Consider real-world examples of increased efficiency with submitting pathways requests with FDA and EMA independently and simultaneously

Who Should Attend:
• Delegates from the regulatory affairs industry who wish to develop their strategic knowledge within this area
• Delegates who want to obtain a better insight into Clinical Trial Programs into the US
• Regulatory Professionals who wish to gain a comprehensive understanding of the subject.
• Less experienced regulatory affairs professionals 

Mara Holinger, PhD, RAC
Senior Vice President, Regulatory Affairs, Veristat



Mara Holinger provides pharmaceutical, biotech and medical device firms with strategic consulting to prepare their regulatory pathway, design their clinical program and trials, perform gap analysis for CMC and preclinical reporting and write regulatory applications.  Additionally, she is an expert in regulatory agency meeting preparation, moderation and logistical support, and services as an Authorized Regulatory Representative and US Agent.   Mara has written, reviewed or provided oversight for more than 20 Investigational New Drug Applications (INDs), multiple Orphan Drug Designation (ODD) applications, breakthrough designation applications, special protocol assessments, fast track applications and several New Drug Applications, including 505(b)(2). 
Mara earned her Ph.D. in Molecular Microbiology from Tufts University School of Medicine and began her career as a lead scientist in anti-cancer research.     
Xavier Luria, MD
Vice President, Regulatory Affairs Europe, Veristat



Xavier Luria, MD, is responsible for providing strategic and implementation counsel across the spectrum of global regulatory and pharmacovigilance services for drugs, IVDs, and medical devices. Levering his deep expertise, Dr. Luria drives productive communication with health authorities and associated meetings and submissions, along with overseeing the development of impeccable project regulatory documentation and safety reporting.

Dr. Luria has nearly a decade of experience offering regulatory consulting within industry, 7 years of experience working as Head of Safety and Efficacy of Medicines at the European Medicines Agency (EMA) and spent the prior 18 years in the pharmaceutical industry.     

In addition to Dr. Luria’s specialty in internal medicine, and pharmaceutical medicine and biostatistics (University Autonomous Barcelona), he has developed expertise in several specific therapeutic areas, carried out postgraduate qualification in clinical pharmacology, drug development and regulation (Tufts University School of Medicine, Boston), and he is a recognized expert on regulatory systems and benefit-risk assessment (modelling, development and methodologies).

Kevin Hennegan, MA
Director of US Regulatory Affairs, Veristat



Kevin Hennegan has provided strategic clinical and regulatory guidance to the pharmaceutical, biotech and medical device industry for over 15 years. He has led and participated in the preparation of many successful FDA filings, including Investigational New Drug Applications (INDs), New Drug Applications (NDAs), Biologics License Applications (BLAs), Breakthrough Therapy Designations, Orphan Drug Designations and Fast Track Applications. His experience covers a wide array of therapeutic indications (oncology, neurology, rheumatology, infectious disease, etc.) and product classes (therapeutic proteins, small molecule drugs, cell therapies, gene therapies, vaccines and more). He is an advocate for patient-focused drug development and excels in engaging the FDA and other regulatory authorities as development partners.

Kevin earned a bachelor’s degree in Microbiology from Colorado State University and a master’s degree in Molecular, Cellular and Developmental Biology from the University of Colorado at Boulder.

Disclaimer: Whilst TOPRA is running this webinar for Veristat, this is not an endorsement of Veristat, Veristat's affiliates, employees or its products and services. TOPRA is also not responsible for the content or views expressed during the webinar.

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