|Quantity Discounts||1 - 9999|
|1 - 9999|
|1 - 9999|
|1 - 9999|
Unfortunately, the FDA guidance doesn’t address the business and technical skills users must have. And to compound matters, FDA continues to tighten its validation criteria for eCTD submissions.
To help you survive, e‑SubmissionsSolutions’ expert Antoinette Azevedo will teach the necessary skills beyond what’s listed in the guidance with her proven eCTD Roadmap.
If you find yourself asking any of these questions — you’re not alone.
Avoid the traps and costly quality assurance mistakes that plague users and companies. Don’t fall victim to thinking that just because you have your in-house eDMS it will be easy to outsource your submission publishing project. All the content needs to be correctly exported so that you don’t lose chain of custody and audit trails.
Your colleagues and competitors have already found the key. Don’t delay. Register now for the encore presentation of eCTD Requirements: Where Are You on The Curve?
Antoinette Azevedo gets rave reviews from industry professionals for her expertise and teaching style:
"Antoinette's expertise in the fields of document management and electronic publishing is unquestionable. She understands all of the potential hurdles — not just current FDA/ICH standards, but also hardware issues, software issues, IT support, need for document control and even the struggles with internal resistance to standardization and change.”
Kathleen Gibbon, Senior Director, Regulatory Affairs, Avera Pharmaceuticals
Attend eCTD Requirements: Where Are You on The Curve? and you will:
This encore presentation is a must for professionals in the drug industry, including
Antoinette Azevedo, founded e‑SubmissionsSolutions.com to advise all sizes of biotechnology and pharmaceutical companies on the use of technology to manage regulatory documents and publish electronic submissions.
She was director of West Coast Operations for Liquent from 1997 to 2000. She was principal consultant in the CSC Consulting life sciences practice as technical lead for regulatory submission publishing from 1994 to 1997, working with pharmaceutical clients both large and small in North America and Western Europe.
|Date:||Feb. 18 – March 8, 2013|
|Location:||Your office or conference room (no need to travel!)|
Gather your team for maximum benefit! Your investment is for one dial-in.
Significant tuition discounts are available for three or more sites from
Call (888) 838-5578 in the U.S. or +1 (703) 538-7600 globally
We accept American Express, Visa and MasterCard. Make checks payable to FDAnews.
Or, register by phone: toll free (888) 838-5578 (inside the U.S.) or +1 (703) 538-7600
Registrations may not be cancelled. Please contact customer service to make any substitutions.
Interested in Becoming a Speaker?
We're always looking for industry leaders eager to share their expertise at an FDAnews audioconference, webinar or physical conference. Our seasoned speaker community includes executives in the pharmaceutical, medical device and clinical trial industries, regulatory affairs, quality control, compliance, healthcare and academia, as well as several former — and current — top FDA officials. Click here to complete our speaker opportunity form and have a representative contact you about future opportunities.
"Antoinette is extremely knowledgeable regarding needs across the industry."
Report Coordination Supervisor, SNBL USA
"Antoinette knows the topic well, was very helpful and open to questions and suggestions. She led the discussion well and provided a wealth of information. The workshop materials were very comprehensive with good handouts, takeaways and valuable tools."
Director, Regulatory Submissions
“With over 20 years in the industry, Antoinette brings a wealth of experience and knowledge in the electronic submissions and document management areas. In the past 10 years, I have drawn on Antoinette's expertise for large and small electronic submission and document management projects. Each time, she has delivered above my expectations. She is respected in the pharmaceutical industry as a subject matter expert for electronic submissions to health authorities. It is her experience, knowledge and work ethic that has earned her that respect."
Director, Operations and Regulatory Information Management, Regulatory Affairs
"Ms. Azevedo is a longstanding, industry-recognized subject matter expert in regulatory submissions to the FDA and international regulatory agencies. Ms. Azevedo is unique in the regulatory submissions industry in that she provides her clients with strategies for regulatory submissions. This clearly differentiates her from many other providers. Bottom line, I take my business to e‑SubmissionsSolutions.com for regulatory submissions solutions. And when it comes to paperless, eCTD filings, Ms. Azevedo is the ‘go to’ authority. Just ask what clients retain her business. If top global biotech and pharmaceutical firms can rely on Antoinette, we all can. I do."
Steven Gerken, Ph.D., MBA
"Antoinette is a great resource for eCTD and has been very valuable to our organization. Her feedback is very helpful and her technical knowledge is outstanding!"
Manager, Regulatory Document Operations
Takeda Global Research & Development Center
Copyright ©2018. All Rights Reserved. Design, CMS, Hosting & Web Development :: ePublishing