Preparation of FDA Submissions and Communicating with the FDA

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    "CfPIE instructors always do a great job and are very knowledgeable about the subject/topic area. I really enjoyed the information related to IND meetings and FDA interactions."


    Kevin Hadley, Senior Clinical Research Scientist, DSM Nutritional Products

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    "Very good course, interactive and very useful for regulatory professionals. It covered all points from agenda and complied with the objectives. This course helped me to better understand FDA regulations."


    Maria R., Regulatory Affairs Manager, Probiomed S.A. de C.V.

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    "The Course Director did a great job in keeping us engaged. I most enjoyed the specific examples that were presented within the different topics covered throughout the course. The course content was very thorough, as well as current (updated). This is very important in this field. After attending the course, I have a better understanding on how to prepare/ communicate for FDA interactions. I enjoyed the course very much. He is a great, very knowledgeable instructor!"  


    Daphne, Scientist, Janssen R&D

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    "This course gave a great overview and insight into requirements for submissions and working with the FDA. The Course Director's experience provided additional insight that was appreciated!"  


    Amy H., Regulatory Affairs Manager, Cardinal Health

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Course Director

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Course Fee

$2150.00 Regular Registration

$1950.00 Early Bird Pricing (Register 30 Days in Advance)

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Course Description

This 15-hour FDA regulatory submission requirements training will give participants the necessary overview of the US Food and Drug Administration's (FDA) current responsibilities, procedures, guidances and regulatory pathways that affect the review and approval of chemical drugs, biologicals, biopharmaceuticals, biosimilars and chemical generics. Using the ICH Common Technical Document (CTD) module format outline, significant Chemistry Manufacturing and Controls (CMC), Nonclinical and Clinical areas will be analyzed and discussed, as a basis for strategic planning for both submitting INDs, NDAs, BLAs, ANDAs, and post-approval supplements, as well as for holding key meetings with the FDA.


Similarities and differences between clinical INDs and market approval dossiers, and between the various market approval dossiers (NDAs, BLAs, and ANDAs) will be discussed. Other topics to be discussed include Fast Track pathway, comparison of chemical generics with biosimilars, FDA's commitments under the User Fee Acts (PDUFA, BsUFA, GDUFA) and FDA's evaluation of industry's performance in meeting its requirements and expectations for review of drug products. This certificate not only verifies your commitment to professional development, but it also positions you for greater leadership in regulatory roles, clinical and CMC domains.

Who Should Attend

Personnel in the pharmaceutical, biopharmaceutical, biologics and generic drug industry who are involved in preparing FDA submissions (INDs, NDAs, BLAs, ANDAs, post-approval supplements) will find this FDA submission preparation and communication course to be of particular benefit. Those who need to interact with FDA staff, including Project Managers, Regulatory Affairs, Clinical, Nonclinical, Manufacturing, and Quality personnel, will also find this FDA submission process course extremely useful. 


The course is well-suited to professionals who must align technical content with regulatory strategy before submission reaches the agency. Participants who support dossier planning, meeting preparation or cross-functional review can use this training to better understand how submission decisions affect FDA communication at different stages of development and review. 

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  • Learning Objectives

    By the end of this FDA compliance and submission strategy training course, you'll be able to: 


    Understand the importance and underlying principles of the FDA regulatory review process for chemical drugs, biologics and biopharmaceuticals from Phase 1 IND through market approval

    • Learn how to prepare appropriate and necessary FDA regulatory submissions throughout the drug development process covering the CMC, Nonclinical and Clinical areas
    • Learn how to more effectively communicate with the FDA through submissions and meetings
    • Fully understand the seriousness with which the FDA carries out its responsibilities and the ramifications of either not filing or filing incomplete submissions

  • Agenda


    Legal Basis for FDA’s Authority to Regulate Human Medicines

    • Overview of human medicine regulation by the FDA
    • Drug regulatory pathways granted to the FDA by U.S. Congressional laws
    • Human medicine distinctions:  chemical drugs vs. biologics, CDER vs. CBER, generics vs. biosimilars

    FDA Review/Control of Human Drug Development & Accelerating Development and FDA reviews

    • FDA's requirements/expectations for CMC, Nonclinical, Clinical content from Phase 1 through market approval
    • Differences in the FDA regulatory review and approval pathways for NDAs, BLAs, ANDAs and biosimilars
    • Accelerated and fast track FDA review opportunities 

    Meetings With the FDA – Critical Importance of Communications During Clinical Development and Marketing Applications

    • PDUFA, BsUFA, GDUFA meetings with the FDA - justified not entitled
    • Risk assessment – when should you have a meeting with the FDA
    • Lessons learned of what to do/not to do
    • What the FDA is looking for in IND submissions/amendments – avoiding the 'clinical hold'  
    • Forms, format and content required during the clinical stages 
    • Strategic value of the End-of-Phase 2 (EOP2) meeting with the FDA

    Critical Importance of the IND/NDA/BLA/ANDA Dossier Preparation

    • Need to avoid the Refusal to File
    • What the FDA is looking for in the market application dossier – forms, format, content  
    • Strategic value of the Pre-NDA/BLA submission meeting with the FDA  

    FDA Review and Approval of NDA/BLA/ANDA Submissions

    • First milestone – avoiding the 'Refusal to File'
    • Intense interactions with the FDA covering CMC, Nonclinical and Clinical
    • Race to meet the time clock – avoiding the Complete Response Letter

    Post-Market Approval Submissions and Interactions with the FDA

    • Supplements for changes in CMC and Clinical, and required FDA reporting/updating 
    • Problem reporting: Field Alert Reports (FAR), Biologic Product Deviation Report (BPDR), and ORA inspections
    • Honoring post-market approval commitments and ongoing adverse event reporting

    Navigating the Rich FDA Website Resources

    • On-line resources for Drugs
    • On-line resources for Biologics
    • Insights into the FDA NDA/BLA review process

  • Testimonials

    "CfPIE instructors always do a great job and are very knowledgeable about the subject/topic area. I really enjoyed the information related to IND meetings and FDA interactions."

    Kevin Hadley, Senior Clinical Research Scientist, DSM Nutritional Products


    "This course was very comprehensive, interactive, and had plenty of supporting documentation.  I really enjoyed the class discussions."

    Sabrina D., Scientific Writer, Carisma Therapeutics


    "This was a well-balanced and complete course and very well structured. The tips and lessons learned were very useful."

    Olivier B., Senior Regulatory Affairs Associate, Ablynx NV


    "I was very impressed with the breadth and depth of knowledge the course director had!"

    Jennifer, Regulatory Affairs Specialist, Liebel-Flarsheim Company LLC


    "My expectations were exceeded with this course. I definitely recommend this for all pharma professionals who are keen to develop their skills in contacting the FDA and to learn how his communication process works."

    Carlos V., Early Development Manager, Ache Laboratorios Farmaceuticos


    "This was an excellent course even for seasoned professionals. This course offers a great overview of the current regulatory environment while also promoting interactions between industry professionals. A great course for professional development."

    Rachael G., Regulatory Associate, USWorldMeds


    "Very good course, interactive and very useful for regulatory professionals. It covered all points from agenda and complied with the objectives. This course helped me to better understand FDA regulations."

    Maria R., Regulatory Affairs Manager, Probiomed S.A. de C.V.


    "I liked the course organization and the material. The communication with the Course Director was very easy."

    Erica L., Regulatory Affairs Specialist, Probiomed S.A. de C.V.


    "The Course Director did a great job in keeping us engaged. I most enjoyed the specific examples that were presented within the different topics covered throughout the course. The course content was very thorough, as well as current (updated). This is very important in this field. After attending the course, I have a better understanding on how to prepare/ communicate for FDA interactions. I enjoyed the course very much. He is a great, very knowledgeable instructor!"

    Daphne, Scientist, Janssen R&D


    "This course was pretty intuitive with very good, real-life examples. I like the global perspective incorporated into the presentation slides."

    Lara N., Director, Regulatory Affairs, Nexgen Pharm


    "Very thorough. We covered a large amount of information and the Director was knowledgeable and willing to answer a wide range of questions."

    Vincent A., Regulatory Affairs Manager, Prestige Brands


    "Thoroughly enjoyed the course. Course Director presented and spoke at a good pace to keep your interest peaked. Now have a much better understanding of the submissions process. Knowledge gained in this course will help in my day-to-day work life."

    Joanne A., Sr. Medical Affairs Coordinator, Bayer


    "This was a very well organized course. The pace was perfect and it provided a wealth of information to enhance my ability to file INDs and NDAs. This course was well worth the cost and time away from work."

    Dr. Sandra W., Research Fellow, Merck


    "This course was a great overview of the submission process. Has been very informative, as my company is preparing for an IND filing."

    Caitlin C., QA Document Control Specialist, Celtaxsys


    "The Course Director was an excellent trainer and presenter. The course was fabulous, and I have a very good understanding of the material. The materials, media, internet references will all be put to good use. Thank you for the great experience - I am ready to apply my knowledge!"

    Stacey H., Sr. QA Associate Regulatory Affairs, Gallus BioPharmaceuticals


    "The content of the course was exactly what I was looking for – comprehensive review with practical applications through real-life examples. The knowledge base and personal experience of the instructor and ability to make the course interactive provided an optimal learning environment on a somewhat heavy topic."

    Jim C., Director, Medical Research, Pfizer


    "The course director was incredible and thoroughly versed in the subject matter. Top notch trainer!"

    Yvonne S., QA Document Manager, Inst. For One World Health


    "Very personable Course Director. Held the attention of the class. Very well-organizaed and prepared. Course Notes were well organized. Able to handle questions well and present ‘real-life' experiences."

    Angela S., Medical Writer, Abbott Laboratories


    "Always nice to see actual or mock documents of how things look eCTD, CTD, slides of pre IND meeting examples. Thank you so much, the course was very well done!"

    Tammy L., Regulatory Affairs Senior Manager, Ultradent Products


    "This course gave a great overview and insight into requirements for submissions and working with the FDA. The Course Director's experience provided additional insight that was appreciated!"

    Amy H., Regulatory Affairs Manager, Cardinal Health


    "Very comprehensive and easy to understand!"

    Carl D., Team Leader of Regulatory Affairs, The Dial Corp.


    "The speaker was superior. Seldom do I go to a course where the speaker does not read the overheads word for word. Super, Super, Super!"

    Chandler W., Manager, Analytical Services, Stability Group


    "The Course Director articulated his ideas and the course content in a manner that was concise and interesting. This was the best course and instructor that I have been exposed to thus far. Excellent speaker…great job!"

    Lynn C., Regulatory Affairs Associate, Biomira


    "Great balance of overview of a high amount of material, but also a lot of specific, practical advice."

    Sean O., QA/Regulatory Compliance, MD Andersen

FAQs

  • How much of the course deals with INDs and how much with NDAs/BLAs?

    The FDA compliance and submission strategy training covers both IND and NDA/BLA in great detail. You'll learn everything from submission of original INDs, through IND amendments, FDA meetings during clinical development, preparation of the market approval dossier (NDA, BLA, ANDA) and maintenance of the market approval. 

  • Does the course cover CMC, nonclinical and clinical concerns?

    Yes, the course covers FDA concerns and expectations for CMC, nonclinical (i.e., animal studies) and clinical (i.e., human studies). 

  • I am new to regulatory issues. Will I understand what is being presented?

    Yes, the course is suitable for both newcomers and experienced professionals in the field. The course systematically covers all aspects of FDA submissions and communications in three layers. The first layer is a broad overview, and the remaining two layers each dig deeper into understanding the FDA concerns. 

  • Our company is preparing for its first IND filing. Is this course appropriate for this stage, or is it better suited for those further along in development?

    The pharmaceutical FDA approval submission course is well-suited to teams at exactly that stage. It covers the full submission life cycle, beginning with the regulatory framework and FDA's expectations for IND preparation, so first-time filers will get a clear, structured understanding of what's required before they submit. The depth of content covering NDA, BLA and post-approval obligations means the course remains valuable as your program advances.

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Registrant Information:

Each person attending a course will be asked to set up an Attendee Profile Account during the registration process. Creating an Account helps you view your order history and manage your training programs. If you are registering for others, please set up an Account in the Attendee’s name. If you are registering more than one person, you’ll need to set up a separate account for each Attendee.