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Best Practices in Clinical Pharmacology Gap Analysis

WEBINAR DETAILS

Date: Wednesday, November 15, 2017

Time: 11am EST / 4pm GMT (UK) / 5pm CET (EU-Central)

Duration: 60 minutes

Featured Speaker:

Submitting your New Drug Adminstration (NDA) to the US Food and Drug Administration (FDA) is the ultimate test of a drug program. Are you confident that you'll have robust answers to the 40 different questions that the agency will ask about your clinical pharmacology data package at the time of an NDA submission? If the thought gives you "pre-test jitters,"¯ you might want to invest in a clinical pharmacology gap analysis– a tool that can help you evaluate and address any potential gaps in your program before the FDA does.

The field of clinical pharmacology can help stakeholders address these challenges and improve decision-making at critical milestones, whether early in proof-of-concept phases (preclinical through 2a clinical trials) or in the later stages where a more robust risk and efficacy profile is established (2b through 3 clinical trials). The tools, methods, and frameworks (e.g., mechanistic or quantitative) of clinical pharmacology span distinct sub-specialties and can significantly impact these preclinical and clinical phases.

Attend this webinar to learn from Dr. Julie Bullock, Senior Director of Consulting Services at Certara, how gap analysis can help you ensure that your development program will contain all the elements needed to satisfy regulators and investors during all phases of drug development from Investigational New Drug (IND) to NDA. By attending this webinar, you will learn the following:

  • What questions the agency will ask about your clinical pharmacology data package at the time of an NDA submission
  • How gap analysis can help you develop a clinical pharmacology development strategy that covers all relevant domains
  • What data to gather and when to gather it to enhance decision-making during development
  • How a clear clinical pharmacology plan can assist in negotiations with regulators and investors during IND development
  • What quantitative analyses (pharmacometrics and other model-informed drug development technologies) can be leveraged to diminish dedicated study needs and accelerate your path to drug approval
ABOUT OUR SPEAKER

Julie Bullock, Senior Director of Consulting Services, Certara


Dr. Bullock has over 10 years of drug development experience within the FDA. Dr. Bullock's past appointments include Clinical Pharmacology Team Leader and Senior Clinical Pharmacology Reviewer (FDA). Her regulatory experience was focused in the therapeutic areas of hematology/oncology and coagulation. She has unique insight in pediatric development, PK/PD approaches for biosimilar products, oncology dose finding strategy and streamlining development for breakthrough therapies and accelerated approval. Dr. Bullock has contributed to over 14 new molecular entity approvals during her 10 year FDA career.

THIS PROGRAM IS INTENDED FOR

This program is intended for professionals from pharmaceutical and biotech companies involved in regulatory affairs, medical affairs, and research & development.

OUR XTALKS PARTNER FOR THIS EVENT

Certara is a leading decision support technology and consulting organization committed to optimizing drug development and improving health outcomes. Certara's solutions, which span drug discovery through patient care, use the most scientifically-advanced modeling and simulation technologies and regulatory strategies to increase the probability of regulatory and commercial success. Its clients include hundreds of global biopharmaceutical companies, leading academic institutions, and key regulatory agencies.

 

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