Request for proposals to manage the Embase Search Project

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					Request for Proposals (RFP) to manage the
Embase Search Project

RFP release date: Monday, September 17th, 2012
Deadline for proposals: Friday, October 26th, 2012


1. Overview
This Request for Proposals (RFP) to manage the Embase Search Project is aimed at Cochrane entities
and organisations associated with The Cochrane Collaboration. The work maybe particularly suited
to a Cochrane Centre but proposals from any entity or organisation are welcomed. The contract with
the successful bidder will be awarded for one year in the first instance, with a review at the end of
this period and the possible option to renew for a further period. Bidders will be judged on:

       I.   Their ability to ensure delivery of the outputs accurately
      II.   The proposal of a credible process to ensure outputs
     III.   The demonstration of capacity, and the capability of the staff on the project
     IV.    Cost effectiveness of the solution
      V.    Their familiarity with The Cochrane Collaboration and its needs


2. Background
“Embase is a... database covering the most important international biomedical literature from 1947
to the present day” i

From 1997 to 2011, the UK Cochrane Centre (UKCC) managed the Embase Search Project on behalf
of the Collaboration, conducting annual searches of Embase to identify records that were not
already indexed as randomised trials in MEDLINE. These searches have been completed for the
years 1980 to 2010. In total, they have yielded over 100,000 additional unique reports of trials not
indexed at the time of the search.

All of these records are now published in the Cochrane CENTRAL Register of Controlled Trials
(CENTRAL) under a Licence Agreement between Elsevier, the publisher of Embase; and John Wiley &
Sons, Ltd (Wiley), the publisher of The Cochrane Library. As part of this agreement, a complementary
subscription to Embase - via Ovid - is available for the purpose of the Embase Search Project to the
group designated by the Collaboration to manage it.

In 2011, with guidance from funders, the UKCC decided not to continue to manage the project,
although they completed the processing and submission of the journal article records in the 2010


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dataset. For the first time conference abstracts were included, which Elsevier had newly added to
Embase in 2010, increasing considerably the number of records retrieved. For the 2010 dataset,
approximately 42,000 potentially eligible records were retrieved, when ordinarily this would have
been expected to be around 23,000 to 24,000. A pilot study, looking at approximately 4000 of these
records was undertaken to investigate how many might be eligible for inclusion in CENTRAL. Some of
these records were processed by the UKCC before work on Embase ceased.


3. Instructions to bidders
          3.1. Proposals


   Proposals are encouraged from bidders that meet the solution outlined in this paper, as it
   represents the Collaboration’s view of its requirements based on current practices. Other
   innovative or alternative solutions may also be proposed that will achieve the ultimate aim of
   the user requirements outlined in the Summary of business needs. Alternative solutions must
   have sufficient detail to enable comparison. Value-for-money will be a key consideration.


          3.2. Tender response


   Proposals should be provided as attachments to an email to Ruth Foxlee, Information Specialist,
   The Cochrane Editorial Unit: rfoxlee@cochrane.org.


          3.3. Summary of business needs


   Since 1997, the Embase Search Project has been fundamental to the composition of CENTRAL,
   which is a key component of the evidence base on which Cochrane and many other systematic
   Reviews are built. The implementation of the Cochrane Register of Studies (CRS), the
   Collaboration’s online software for managing specialized registers of healthcare studies and their
   reports, has resulted in a change in the publication cycle of CENTRAL.

   In January 2012, CENTRAL moved from a quarterly to monthly publication cycle via the CRS. This
   cycle includes monthly searches of MEDLINE, which are being carried out by the Collaboration’s
   development partner for the CRS, Metaxis Ltd. The ability to establish an accelerated process for
   identifying and processing Embase records will be important consideration in assessing bidders’
   proposals. The additional work involved in shifting to a monthly publication cycle has been
   accounted for in the indicative budget (see item 3.6).

   In the 2011 for the first time, the entire Medline dataset was included within the Embase
   dataset. The proposal of a method to handle this change will be considered an essential
   component of any proposal.

   In their proposals, bidders should set-out how they intend to provide the following services:


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     I.     The identification of reports of randomized controlled trials (RCTs) and quasi-
            randomized controlled trials (QRCTs) in Embase that have not already been indexed with
            the Publication Types “Randomized Controlled Trial” and “Controlled Clinical Trial” in
            Medline, from 2011 onwards.
    II.     Processing of the remainder of the 2010 dataset, comprising conference abstracts only,
            which was not completed at the time the UKCC ceased to carry out this work.
    III.    Timely delivery of the records in tagged text format on a monthly basis to Metaxis Ltd.
            This will be on a monthly cycle for the foreseeable future but the successful solution
            should also have the capability of delivering records on a ‘publish when ready’ basis.
    IV.     Processing of the 2011 and 2012 datasets (including conference abstracts) to bring the
            project up to date. This “catch-up” processing must feed into the monthly publication
            cycle.
    V.      Annual reassessment of the search strategy to identify relevant studies to take into
            account changes in indexing terms and enhancements to database content, structure
            and functionality, and adjustments to the design of the strategy required to ensure trial
            identification remains methodologically sound.


           3.4. Operational requirements


The successful bidder will be responsible for:

           Designing (including annual reassessment) and running searches
           Developing and updating configuration files
           Downloading, preparing and distributing records to a handsearcher(s) (for the coding of
            reports as RCT or Quasi-RCT or not eligible)
           Recruitment of appropriately skilled handsearchers
           Quality control of handsearching (for verification of coding)
           Creating and submitting eligible records to Metaxis Ltd (CRS) for publication in CENTRAL
           Supporting colleagues from Wiley in the negotiation of contracts with Elsevier


           3.5. Project plan



Bidders should provide a detailed outline of how they intend to achieve the requirements
outlined above. The project plan should include:

      Information about the search methods the bidder intends to use, shown in enough detail to
       allow the Collaboration to assess whether or not the project proposal is underpinned by an
       appropriate level of search methodological expertise
      Names and summaries of the relevant experience of the staff to be employed on the project
      Details of the bidder’s relevant experience in the delivery of similar solutions to that outlined by
       this RFP


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A template for completing responses is provided at the bottom of this document.

      3.6. Project budget



The Cochrane Collaboration Steering Group has approved a budget for three years for this
project. The indicative funding amount is 30K GBP for the first year with a further indicative
budget of 14K GBP for the second and third years. The successful proposal will provide a cost
effective solution which meets the Collaboration’s need for identifying unique reports of trials in
Embase and delivering them to Metaxis Ltd for publication in CENTRAL. It is envisaged that the
majority of the budget will be allocated to staffing costs, though a proportion of the budget may
relate to equipment. Travel costs will not be funded.

Bidders will provide full costings for their proposals, including the cost of processing the backlog
of 2010 Embase conference abstract records (approximately 20,000 records) and the ongoing
annual costs of processing Embase records for journal articles and conference abstracts
(approximately 42,000 records). It is likely that bidders who bring forward additional resources
to part-fund their proposals may be received more positively, but the quality of the proposal will
be of paramount importance.

Any staff employed as part of the project would be employed by the bidder and not by The
Cochrane Collaboration


      3.7. Financial and contract considerations


The following considerations apply to this RFP:

        a) The successful bidder will be awarded a contract with The Cochrane Collaboration.
           Award of the project will not be considered finalised until contracts have been
           successfully agreed and signed.
        b) In line with Collaboration policy, and those of other charities, for proposals
           originating in universities and similar institutions, only direct costs (the marginal
           costs of delivering the project) will be funded. Indirect institutional and related costs
           such as ‘estates’ and ‘overheads’ will not be funded.
        c) For proposals originating in Cochrane entities, entity infrastructure costs will not be
           funded, except as required for direct delivery of the proposal.


      3.8. Bidder profile


The bidder should be able to demonstrate experience in the delivery of similar solutions to those
outlined in this RFP or that they have appropriately skilled staff who are capable of developing and
delivering a solution that meets the Collaboration’s needs.



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      3.9. Handover from UK Cochrane Centre



The UKCC can provide the bidder with a set of search terms used in their Embase search strategy
to date. These terms have been objectively derived based on the methods used to revise the
Cochrane Highly Sensitive Search Strategy for Medline; however recent changes to Embase and
the Ovid platform will require that the search strategy itself be adapted before running the 2011
dataset. As noted above, Embase now includes the whole of the Medline dataset; it will be the
responsibility of the bidder to devise a method of retrieving reports of RCTs and CCTs that are
unique to Embase and not also labelled as RCTs and CCTs as publication types in Medline.

As outlined above, selected conference proceedings are now indexed in Embase, which has
added considerably to the number of records retrieved. The conference abstracts downloaded
in the 2010 dataset by the UKCC and not yet processed as part of the pilot study can be passed
on, but the bidder may prefer to run a fresh search to identify records of reports of RCTs or CCTs
that are labelled as conference abstracts in Embase to take advantage of any changes in indexing
and improvements in formatting of these records since the original search was run in January
2011. The successful bidder will have an opportunity to discuss the issues around conference
abstracts in Embase with UKCC staff.




      3.10. Statement of Timescales



Bidder Response to RFP
Bidders’ responses must be delivered to The Cochrane Collaboration (see section 2 b) not later
than 00:00 in their location on Friday, 26th October 2012.

Consideration of Proposals by The Cochrane Collaboration
The Cochrane Collaboration will require a period of time to consider the proposals received.
This process should be completed by Friday, 16th November 2012.

Clarification
During the consideration period the Collaboration will clarify and discuss proposed solutions
with bidders as appropriate.

Decision
The Collaboration hopes to come to a decision within three (3) weeks of the closing date for
proposals. Bidders will be judged on the criteria outlined in Section 1.




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Delivery Schedule
Delivery schedules will be agreed between the bidder and the Collaboration, but proposals
whose deliverables can be delivered successfully at an early date will be welcomed.




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                                 TENDER REPONSE FORM
                                EMBASE SEARCH PROJECT
Entity/organisation name

Entity/organisation contact
details

Names of the staff on the
proposal, including the
project lead
Contact details for the staff
on the proposal



Summary of the
qualifications and
experience of the staff on
the proposal




Details of the proposal
budget




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Detailed project plan




Person authorised to           Signature:
submit the proposal on         Name:
behalf of                      Position in entity/ organisation:
entity/organisation
                               In submitting a proposal, the authorised signatory must affirm that
                               they accept the terms and conditions pertaining to the call; and that
                               there is no legal, financial, ethical or other possible conflict of interest,
                               as usually understood or according to The Cochrane Collaboration’s
                               policies, that would prevent their entity/organisation from
                               participating in this call for proposals; or declare such a conflict so that
                               the implications of this can be considered when the proposal is being
                               assessed.


i
    http://www.embase.com/info/what-embase




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