8806 LIBERTY LANE ° POTOMAC, MARYLAND 20854
° 301-983-0395 °

 
  HOME ::      

 
 
 
 
  
                                                                                                               + A | - A
 
Hot Topics


Pre-IND/IDE Meetings Can Reduce Time to Market - Perspective from a Former "FDA Insider"
January 22 , 11:30 AM - 12:30 PM (EST)
Jerri Barden Perkins, MD, Former FDA Medical Officer
Click here for event flyer

ACRP Annual Meeting in Boston, MA; Errors in GCP's Preventing Nightmares.
Saturday, April 26, 2008
Jerri Barden Perkins, MD, Former FDA Medical Officer.

Excellence in Research : Building a Strong Foundation
Device Misconduct: Hidden Hazards in a Case Study
Friday, September 21, 2007
Jerri Barden Perkins, MD, Former FDA Medical Officer.
Sheraton Columbia Hotel
Wincopin Circle
Columbia, MD.
Click here for event flyer

An FDA Insider's Guide to Pre-IND/IDE Meetings
How to Avoid Clinical Trial Holds
July 19, 2007
Jerri Barden Perkins, MD, Former FDA medical officer
Click here for event flyer

Clinical Trial Nightmares: How to Prevent them with Good Clinical Practices
Thursday, January 11, 2007
Jerri Barden Perkins, MD, Former FDA Medical Officer
VA Hospital, Education Conference Room, 42nd and Woolworth, Omaha, NE

Contemporary Issues in Clinical Research
Building Quality into Clinical Trials (Devices, Drugs & Biologics) + Q&A
September 30, 2006
 Click here for event flyer.

Demystifying the FDA Audit Process:
Perspective from a Former FDA Medical Officer
Followed by: Good Clinical Practices
Workshop and IDE Forum
June 1, 2006
 Click here for event flyer.

How to Prepare for the FDA Clinical Research Audits
February 7, 2006,
Jerri Perkins, M.D., FDA Consultant, Perkins and Perkins.
Click here for flyer.

How to Prepare for an FDA Audit
January 12, 2006
Speakers: Jerri Barden Perkins, M.D., Former FDA Medical Officer
Location: VA Hospital, Education Conference Room, 42nd and Woolworth, Omaha, NE
Click here for flyer.

 
(c) 2008 All rights reserved -Perkins & Perkins Incorporated
 
 
Quick Link
 
 
             

Consultant, FDA, Food and Drug Administration, FDA consultant, FDA audit preparation, fda, FDA Consultant, FDA, Food and Drug Administration, FDA consultant, FDA audit preparation, fda, FDA Consultant, FDA, Food and Drug Administration, FDA consultant, assistance in writing protocols for FDA, FDA regulatory strategy planning, fda consultant, FDA case report forms, FDA applicaton, FDA approval, FDA labeling advice, clinical trail design, advice and preparation of FDA informed consent, FDA patient package inserts, PPI, advice on fda data safety  monitoring board, fda consultant, fda consulting, FDA IND, FDA approval, FDA IDE, fda clinical program evaluation, FDA IND, FDA NDA, FDA IDE, FDA PMA, fda 510(k), fda adverse event report reviews, FDA ISS and IES review and evaluation, fda medical consulting, fda regulatory consulting, GCP Workshops, EXPERT FDA, expert fda, fda medical device consulting, fda consultant, fda approval, fda medical device consulting, fda consultant, fda approval, fda medical device consulting, fda consultant, fda approval, fda medical device consulting, fda consultant, fda approval, fda medical device consulting, fda consultant, fda approval, AIDS, Alzheimer's, Anti-Infective, Cardiovascular Drugs and Devices, Dermatology, GI, Generic Drugs,  Neuropharmacological, Pulmonary Drugs, Barrier Devices, FDA Approval, AIDS Prevention, Drug Device Combinations,  Dental Devices, Gene Therapy, General and Plastic Surgery Devices, GI/GU Devices, Imaging, Lasers,  Neurological and Radiological Devices, OB/GYN, Ophthalmic Devices, fda consultant, Orthopedic Devices, FDA Good Clinical  Practices (GCP) Reviews, assessment for FDA compliance, fda advisory panel preparation, Drug Consultants, Pharmaceutical Consultants, GCP Consultants,  fda regulatory strategy, fda audit preparation, fda pre-approval audit preparation, fda clinical trials, mock FDA inspection, Clinical Quality Assurance Audit, Clinical QA Audit,  Assistance with Clinical Audit, assistance with clinical audit, Pre-FDA Audit, Pre-FDA Inspection, FDA audit, FDA inspection, FDA Medical Consultants in MD, FDA Medical Consultants in Maryland, FDA Regulatory Consultants in MD, FDA Regulatory Consultants in Maryland,  GCP Compliance audit, Good Clinical Practice Compliance Audit, Clinical Trials consultant, Clinical audit experience, former FDA, FDA meeting consultant, FDA drug consultant, FDA drug development, FDA Medical Consultants in DC, FDA Medical Consultants in Washington, DC, FDA Regulatory consultants in Washington, DC, FDA Regulatory consultants in DC