Drug Development: The IND, the IMPD and more. Getting Authorization for Entry Into Man Studies: An Introductory overview of the FDA and EMA Requirements with Reference to other important Regulatory Authorities

Duration:
60 Minutes  
Instructor
Dr. Flavio De Rosa 

In this webinar speaker will give a brief overview of EIM requirement dossiers from other important regulatory authorities will also be provided.

Recorded
Refund Policy

Overview

The aim of this webinar is to provide an introductory overview of the requirements demanded by the FDA and EMA (arguably the two most important regulatory authorities for drug developers) for EIM (the IND and IMPD) and to provide an brief review of where the agencies differ as well the commonalities of approach for their EIM dossiers.

Why you should Attend

Although each regulatory authority publishes guidelines and instructions regarding the requirements for the Entry Into Man (EIM) of a new medication, such information is often located in different pages of the authority's website and it can be time consuming to acquire and review all the relevant information.

The FDA's website, for example, has 27 sections [topics] with a total of 183 subsections, each of which can be multiple pages with links. The EMA website is equally extensive and complex.

A brief overview of EIM requirement dossiers from other important regulatory authorities will also be provided

Areas Covered in the Session

  • The most important regulatory authorities for drug developers
  • What is an IND, what is an IMPD
  • What are the required components for the IND the IMPD dossiers
  • What are the common features to both the IND and the IMPD dossiers
  • Notable differences between the IND and IMPD
  • EIM Requirements for other important regulatory authorities

Who Will Benefit

  • Clinical Scientists
  • Clinical Operations Staff
  • Clinicians and other Medical/Scientific Professionals who support their department of Regulatory Affairs in preparing IND and IMPD dossiers

Speaker Profile

Dr Flavio De Rosa founder of Paracelsus Science GmbH, has more than 30 years of drug development industry experience in all phases of drug development covering diverse therapeutic areas, including oncology, rheumatology and infectiology, and with diverse responsibilities - from drug safety analyses, to advising senior management to study design and conduct.

Academically trained (PhD, MSc. Diploma in Pharmaceutical Medicine) with extensive "hands on" experience in medium and large pharma companies and in a specialised CRO, Dr De Rosa has a broad knowledge of the industry and of medicine and experience working with Key Opinion Leaders. With considerable Clinical Scientist experience in the US, Europe and Australasia (Australia, Malaysia, Japan) he has successfully and consistently delivered complex projects and analyses within set timeframes, budgets and to a very high standard. About Paracelsus Science GmbH;

Paracelsus Science was set up in 2017 to offer support to companies requiring senior specialised staff on a one-off, short- and medium-term basis.
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