Loren Data's SAM Daily™

fbodaily.com
Home Today's SAM Search Archives Numbered Notes CBD Archives Subscribe
SAMDAILY.US - ISSUE OF APRIL 11, 2020 SAM #6708
SOLICITATION NOTICE

D -- PharmaPendium

Notice Date
4/9/2020 1:37:19 PM
 
Notice Type
Presolicitation
 
NAICS
511210 — Software Publishers
 
Contracting Office
NATIONAL INSTITUTE OF HEALTH NIEHS MORRISVILLE NC 27560 USA
 
ZIP Code
27560
 
Solicitation Number
75N9602004092020
 
Response Due
4/13/2020 9:00:00 AM
 
Archive Date
04/28/2020
 
Point of Contact
Luis A. Salas
 
E-Mail Address
Luis.salas@nih.gov
(Luis.salas@nih.gov)
 
Description
THIS IS A NOTICE OF INTENT AND NOT A REQUEST FOR QUOTATIONS. The National Institute of Environmental Health Sciences (NIEHS), Research Triangle Park, NC intends to negotiate on a sole source basis with Elssevier B.V.,Radarweg 29, 1043 NX Amsterdam, The Netherlands, DUNS # 406928382;� �pursuant to FAR 13.106-1(b)(1)- Only One Responsible Source. This purchase is for: License to access the following Pharmapendium modules: Pharmapendium Base FDA Classic Collection Pharmacokinetics module Efficacy module PharmaPendium is a commercial database that has been carefully curated and organized to provide access to comprehensive safety and regulatory data from the Food and Drug Administration (FDA) submissions on pharmaceuticals. PharmaPendium is a database product derived from data in Food and Drug Administration (FDA) and MDL Information Systems (later bought by Elsevier) Cooperative Research and Development Agreement (CRADA) in 2006 and 2007.� PharmaPendium is a unique database that at its core integrates preclinical, clinical and post-market safety data from all the FDA approval packages.�� An FDA drug approval package consists of medical, pharmacological and other data collected as part of the FDA's review of a pharmaceutical.� Pre-1991 FDA approvals exist on microfiche while more recent approvals publically accessible on the web through the FDA Drug Label Database and Drugs@FDA. Unfortunately, the pharmacokinetic, efficacy, toxicology, and adverse event data are buried in�microfiche, PDFs and webpages rendering this information inaccessible and difficult to search.� As a result, FDA worked with MDL Information Systems (Elsevier) to digitize the approval packages and extract all the data elements in order to create a database that integrated the data from the preclinical, clinical and adverse event reports.� As a result, PharmaPendium encompasses a suite of unique content not provided by any other vendor. This notice of intent is not a solicitation or request for quotes. �Notwithstanding, any responsible source that believes it is capable of meeting NIEHS requirement, may submit capability statement.� Responses to this posting must be submitted via email to, luis.salas@nih.gov, by April 13, 2020 at 12PM EST. � A determination by the Government not to compete this quote contract action based upon responses to this notice is solely with the discretion of the Government. information received will only be considered for the purpose of determining whether to conduct a competitive procurement. There is no solicitation package available. For any questions regarding this announcement, please contact Luis Salas at the above email address.
 
Web Link
SAM.gov Permalink
(https://beta.sam.gov/opp/4876bbeaee55418abd603ffcf98776be/view)
 
Place of Performance
Address: Durham, NC 27709, USA
Zip Code: 27709
Country: USA
 
Record
SN05615686-F 20200411/200409230145 (samdaily.us)
 
Source
SAM.gov Link to This Notice
(may not be valid after Archive Date)

FSG Index  |  This Issue's Index  |  Today's SAM Daily Index Page |
ECGrid: EDI VAN Interconnect ECGridOS: EDI Web Services Interconnect API Government Data Publications CBDDisk Subscribers
 Privacy Policy  Jenny in Wanderland!  © 1994-2024, Loren Data Corp.