Description :
The Drug Discovery and Development (but also the biologics and medical device) process is a very complex process with every participant focusing on their particular piece of discovery or development. You can spend a lifetime in your part of the process, without ever understanding the complete picture. While you may hear or see the other parts by interacting with colleagues from other parts of the process you never quite get the whole picture. Add to that, that different regulatory agencies have different requirements and it often feels like pieces of a jigsaw puzzle which you see at random, never quite understanding how they all fit together to get the big picture.
This leaves you confused, causes friction between departments and leaves the company prone to errors and mishaps that can be avoided if you understood what the other parts of the company and an FDA inspector require of you. This in turn results in delayed timelines, product recalls and operational inefficiencies.
This webinar will lay out the whole process systematically and in a simplified manner. It will help you to understand how what you do and your goals and objectives, contribute to the overall success of the company, both in terms of product approval by the FDA or in terms of successful inspection outcomes. At the end of the webinar, you will be able to have better communication with your functional colleagues and the quality and regulatory affairs departments. This will lead to higher quality product, easier approvals, many fewer errors and much less friction between departments. It is a must for anyone that is either joining the Pharmaceutical / Biotechnology / Medical Device industries for the first time, or anyone that is transferring from one part of the company to another part (e.g. from discovery to development and vice versa). Also for international attendees that need to familiarize themselves with the FDA process and how it differs from other regulatory authorities.
Areas Covered in the Session :
Stages of Drug Development and Review
Drug Review Steps Simplified
Reviewing Applications
Accelerated Approvals
Bumps in the Road
The Role of User Fees
The Quality of Clinical Trials
How Drugs are Approved
How does the FDA differ from other regulatory authorities
Frequently Asked Questions about the FDA Drug Approval Process
Who Will Benefit:
This is a fundamental course that will benefit the following people:
Anyone that works or plans to work in Pharmaceutical, Biotechnology or Medical Device Industries will benefit.
Anyone that is already working in the above industries, but is transferring from one part of the industry to another part (e.g. transferring from discovery to development of vice versa)
Anyone that works in companies that support the above industries e.g., IRBs, CROs, Data Monitoring Companies
International attendees that may be familiar with the above process in their country and for their regulatory authorities, but want to learn the process as expected by the FDA
Price tags:
Live
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Recording
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299
The Drug Discovery and Development (but also the biologics and medical device) process is a very complex process with every participant focusing on their particular piece of discovery or development. You can spend a lifetime in your part of the process, without ever understanding the complete picture. While you may hear or see the other parts by interacting with colleagues from other parts of the process you never quite get the whole picture. Add to that, that different regulatory agencies have different requirements and it often feels like pieces of a jigsaw puzzle which you see at random, never quite understanding how they all fit together to get the big picture.
This leaves you confused, causes friction between departments and leaves the company prone to errors and mishaps that can be avoided if you understood what the other parts of the company and an FDA inspector require of you. This in turn results in delayed timelines, product recalls and operational inefficiencies.
This webinar will lay out the whole process systematically and in a simplified manner. It will help you to understand how what you do and your goals and objectives, contribute to the overall success of the company, both in terms of product approval by the FDA or in terms of successful inspection outcomes. At the end of the webinar, you will be able to have better communication with your functional colleagues and the quality and regulatory affairs departments. This will lead to higher quality product, easier approvals, many fewer errors and much less friction between departments. It is a must for anyone that is either joining the Pharmaceutical / Biotechnology / Medical Device industries for the first time, or anyone that is transferring from one part of the company to another part (e.g. from discovery to development and vice versa). Also for international attendees that need to familiarize themselves with the FDA process and how it differs from other regulatory authorities.
Areas Covered in the Session :
Stages of Drug Development and Review
Drug Review Steps Simplified
Reviewing Applications
Accelerated Approvals
Bumps in the Road
The Role of User Fees
The Quality of Clinical Trials
How Drugs are Approved
How does the FDA differ from other regulatory authorities
Frequently Asked Questions about the FDA Drug Approval Process
Who Will Benefit:
This is a fundamental course that will benefit the following people:
Anyone that works or plans to work in Pharmaceutical, Biotechnology or Medical Device Industries will benefit.
Anyone that is already working in the above industries, but is transferring from one part of the industry to another part (e.g. transferring from discovery to development of vice versa)
Anyone that works in companies that support the above industries e.g., IRBs, CROs, Data Monitoring Companies
International attendees that may be familiar with the above process in their country and for their regulatory authorities, but want to learn the process as expected by the FDA
Price tags:
Live
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Recording
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299
