Gartner IT Analysis & Research provides a unique member-guided research agenda that allows members to glean best practices in IT management and executive-level strategy from a comprehensive and cross-functional perspective.The ERDC requires the acquisition of a Gartner Research subscription to obtain access to research content and advisory services.
Collaboration withpartners and funding agencies, preparation of written reports andpresentations of results shall be elements of provided services.The hub national laboratory for the MSIPP is SRNL.
Group 2: General Questions Instructions: 2.1 Are you presently or have you been debarred, suspended, proposed for debarment, or declared ineligible by any governmental department or agency, whether international, national, state, or local?
The highest priority is to secure a central system for research administration that improves efficiency within the MSU research administration (RA) enterprise. We seek best practice models currently in use at major research universities and/or private industry. Offerors are strongly encouraged to respond with functional details and to convey how their service would work to best meet our needs.
The highest priority is to secure a central system for research administration that improves efficiency within the MSU research administration (RA) enterprise. We seek best practice models currently in use at major research universities and/or private industry. Offerors are strongly encouraged to respond with functional details and to convey how their service would work to best meet our needs.
Event NameState Policy HMO Conversion Research Business UnitHealth Department Event ID2000015747 Event StatusPosted Buyer NameMiller,Barbara E Sealed EventYes Multiple BidsNot Allowed Contact InformationAlisha Simon DescriptionThe 2023 Legislature passed a bill (HF 402, 93rd Legislature) that directs the Minnesota Department of Health (MDH) to complete a study on the potential conversion of nonprofit Health Maintenance Organizations (HMOs) to for-profit
Research Clinical Trial Services Project Description :Proposal for oversight of clinical trial compliant with International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Guideline for Good Clinical Practice (GCP) E6(R2), Health Canada’s Food and Drug Regulations, Part C, Division 5, Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans – TCPS 2 (2022) and other applicable regulations
