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Blog & Resources Camargo Blog Regulatory

The Camargo Blog

Get insight and information from our team of experts to improve your pharmaceutical development and commercialization strategy.


October 3rd, 2011

Don’t Launch Unapproved Products After 9/19/2011

September 11th, 2011

AB Rated 505(b)(2)’s

August 7th, 2011

2012 PDUFA User Fees

June 24th, 2011

Whew! Supreme Court Rules Generic Labels Must Track RLD

June 14th, 2011

K-V’s Makena Part 4: Statistical versus Clinical Significance

June 2nd, 2011

Ophthalmics: 21 CFR 314 94(a)(9)(iv) No Longer Applies

June 2nd, 2011

Why Generic Companies Might Like 505(b)(2)

May 31st, 2011

K-V’s Makena: Part 3: Use of Public Information for 505(b)(2) Approvals

May 23rd, 2011

K-V’s Makena Part 2: Accelerated Approval Subpart H

May 18th, 2011

K-V’s Makena® Part 1: 505(b)(1) or 505(b)2)?

May 16th, 2011

K-V’s Makena®: A trove of 505(b)(2) Lessons

March 23rd, 2011

Revised Safety Reporting for BE/BA Studies Effective March 28, 2011

March 10th, 2011

User Fee Waivers: What is an Affiliate? New Guidance Issued

February 21st, 2011

Approvals of ANDAs Slows

February 1st, 2011

Injectables: 505j or 505(b)(2)?

January 19th, 2011

REMS for 505(b)(2) Products?

January 6th, 2011

2010 505(b)(2) Approvals

December 20th, 2010

PDUFA Fee Waiver: Plan Ahead

December 13th, 2010

Use of Pharmacokinetic n(PK) Modeling & Steady-State Simulations in 505(b)(2) Drug Development

October 18th, 2010

Company Officials Personally Liable

October 15th, 2010

When is an IND Required?

October 6th, 2010

505(b)(2)s with Minimal Sponsor Studies

October 5th, 2010

Why have a Quality Overall Summary for the Quality Module?

August 31st, 2010

Failed 505(b)(2)?: Vivus™ Qnexa

Page 5 of 10


Camargo Pharmaceutical Services provides comprehensive drug development solutions, specializing in customized programs including the 505(b)(2) pathway.


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