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Dante Resources, Inc. Blog

Clinical and regulatory submission related content based on Dante Resources 20 years of successful CTD, eCTD submissions.

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Dante Resources, Inc. Blog | danteresources.blogspot.com Reviews

https://danteresources.blogspot.com

Clinical and regulatory submission related content based on Dante Resources 20 years of successful CTD, eCTD submissions.

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1

Dante's Informative Posts

http://danteresources.blogspot.com/2010/08/dantes-informative-posts.html

Dante Resources, Inc. Blog. Dante Resources is a clinical research organization specializing in regulatory submissions with deep expertise in phase III clinical trial data preparation and submission. The Dante Resources blog content is drawn from Dante Resources over 20 years of successful CTD, eCTD regulatory submissions without a single refusal to file. Thursday, August 26, 2010. Will be back in September 2010. Enjoy the rest of a safe and sunny summer. From the desk of Dante Resources, Inc.

2

Differences in EU and US 510(k) Market Approval

http://danteresources.blogspot.com/2010/06/differences-in-eu-and-us-510k-market.html

Dante Resources, Inc. Blog. Dante Resources is a clinical research organization specializing in regulatory submissions with deep expertise in phase III clinical trial data preparation and submission. The Dante Resources blog content is drawn from Dante Resources over 20 years of successful CTD, eCTD regulatory submissions without a single refusal to file. Monday, June 28, 2010. Differences in EU and US 510(k) Market Approval. Critique medical device design. In the US, a 510(k) application is submitted to...

3

Development of Antibody-Based Therapeutics

http://danteresources.blogspot.com/2010/07/development-of-antibody-based.html

Dante Resources, Inc. Blog. Dante Resources is a clinical research organization specializing in regulatory submissions with deep expertise in phase III clinical trial data preparation and submission. The Dante Resources blog content is drawn from Dante Resources over 20 years of successful CTD, eCTD regulatory submissions without a single refusal to file. Friday, July 16, 2010. Development of Antibody-Based Therapeutics. Posted by Diane Mauriello, PhD. Subscribe to: Post Comments (Atom).

4

July 2010

http://danteresources.blogspot.com/2010_07_01_archive.html

Dante Resources, Inc. Blog. Dante Resources is a clinical research organization specializing in regulatory submissions with deep expertise in phase III clinical trial data preparation and submission. The Dante Resources blog content is drawn from Dante Resources over 20 years of successful CTD, eCTD regulatory submissions without a single refusal to file. Monday, July 19, 2010. Lixiviant Product Development and FDA Regulation. Testing required, such as but not limited to:. Posted by Diane Mauriello, PhD.

5

FDA CDRH 513(g) Medical Device Classification and Clinical Submission

http://danteresources.blogspot.com/2010/07/fda-cdrh-513g-medical-device.html

Dante Resources, Inc. Blog. Dante Resources is a clinical research organization specializing in regulatory submissions with deep expertise in phase III clinical trial data preparation and submission. The Dante Resources blog content is drawn from Dante Resources over 20 years of successful CTD, eCTD regulatory submissions without a single refusal to file. Wednesday, July 7, 2010. FDA CDRH 513(g) Medical Device Classification and Clinical Submission. Protocol, process, procedure. CE Mark - Europe. Within ...

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Darr; Skip to Main Content. 518) 557- 3502 eBiz ROI, Inc. 30 Rosemere Rd, Ballston Lake, NY 12019 Support@eBizROI.com. Business New Website and Website Redesign Client Sample. Bay Colony Advisory Group. Internet marketing client, Bay Colony Advisors, Inc. – Website Redesign project. McKeon and Associates, LLC. Internet marketing client, McKeon and Associates, LLC – New Business Website. Pharmaboard Partners, LLC. Internet marketing client, Pharmaboard Partners, LLC – Website Re-design Project. Click an i...

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Dante Resources, Inc. Blog

Dante Resources, Inc. Blog. Dante Resources is a clinical research organization specializing in regulatory submissions with deep expertise in phase III clinical trial data preparation and submission. The Dante Resources blog content is drawn from Dante Resources over 20 years of successful CTD, eCTD regulatory submissions without a single refusal to file. Thursday, August 26, 2010. Will be back in September 2010. Enjoy the rest of a safe and sunny summer. From the desk of Dante Resources, Inc. HDE amendm...

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