OPDR definition

OPDR means Offset Project Data Report.
OPDR means Offset Project Development Report.
OPDR means Offset Project Development Report. (30) “OPO” means Offset Project Operator.

Examples of OPDR in a sentence

  • Rb. Rotterdam 2 februari 2005, ECLI:NL:RBROT:2006:BD0843, S&S 2008/33 (OPDR Lisboa).

  • Rb. Rotterdam 6 augustus 2014, ECLI:RBROT:2014:7079; Rb. Rotterdam 2 februari 2005, ECLI:NL:RBROT:2006:BD0843, S&S 2008/33 (OPDR Lisboa); ▇.▇.

  • The OPDR, DLCD, and JURISDICTIONS will participate and execute responsibilities and tasks as set forth in this SOW.

  • Once the training event is completed, the Training Organization shall have ten (10) days to enter each participant into the OPDR as having attended that event.

  • If Training Organization is using materials that are copyrighted by the University, such materials may only be used for trainings that will be recorded in the OPDR database.

  • The parties further agree and warrant that there will be no form of recording conducted of any part or all of the OPDR process including any private sessions between the mediator and a party and will ensure that no other person is recording or is able to record any part of the OPDR process.

  • The fee includes prior reading and preparation, the relevant Stage of the OPDR process and administration.

  • The remainder of this Scope of Work (SOW) describes in detail how JURISDICTIONS will partner and collaborate with the OPDR to update the MNHMP.

  • July – September 2019 Task 3.1 Product(s): MNHMP Steering Committee Meeting Task 3.2: OPDR will utilize the prior Risk Assessment and the most recent Lincoln County Hazard Analysis to update the hazard probability and vulnerability scores.

  • DLCD has received a FEMA Pre-Disaster Mitigation grant to assist Lincoln County, the Cities of Depoe Bay, Lincoln City, Newport, Siletz, Toledo, Waldport, and Yachats, as well as Central Lincoln Public Utility District, and Seal Rock Water District (“Jurisdictions”) with updating the Lincoln County Multi-Jurisdictional NHMP and has contracted with the University of Oregon’s Oregon Partnership for Disaster Resilience (OPDR) to execute that assistance.


More Definitions of OPDR

OPDR means Offset Project Data Report. “SSR” means GHG sources, sinks, and reservoirs.
OPDR means the Odisha Public Demand Recovery Act, 1962;

Related to OPDR

  • Treatability study means a study in which a hazardous waste is subjected to a treatment process to determine: (1) Whether the waste is amenable to the treatment process, (2) what pretreatment (if any) is required, (3) the optimal process conditions needed to achieve the desired treatment, (4) the efficiency of a treatment process for a specific waste or wastes, or (5) the characteristics and volumes of residuals from a particular treatment process. Also included in this definition for the purpose of the § 261.4 (e) and (f) exemptions are liner compatibility, corrosion, and other material compatibility studies and toxicological and health effects studies. A “treatability study” is not a means to commercially treat or dispose of hazardous waste.

  • Target Population means persons with low incomes who have one or more disabilities, including mental illness, HIV or AIDS, substance abuse, or other chronic health condition, or individuals eligible for services provided pursuant to the Lanterman Developmental Disabilities Services Act (Division 4.5 (commencing with Section 4500) of the Welfare and Institutions Code) and may include, among other populations, adults, emancipated minors, families with children, elderly persons, young adults aging out of the foster care system, individuals exiting from institutional settings, veterans, and homeless people.

  • Phase III Clinical Trials means a Clinical Trial for the Product on sufficient numbers of patients to generate safety and efficacy data to support Regulatory Approval in the proposed therapeutic indication, conducted in accordance with current good clinical practices and in accordance with a protocol that has been reviewed by the FDA and reflects any comments or concerns raised by the same.

  • Phase III Clinical Trial means a human clinical trial of a product, the design of which is acknowledged by the FDA to be sufficient for such clinical trial to satisfy the requirements of 21 C.F.R. 312.21(c) (as amended or any replacement thereof), or a similar human clinical trial prescribed by the Regulatory Authority in a country other than the United States, the design of which is acknowledged by such Regulatory Authority to be sufficient for such clinical trial to satisfy the requirements of a pivotal efficacy and safety clinical trial.

  • Phase III Clinical Study means a human clinical study of a product on a sufficient number of subjects that is designed to establish that such product is safe and efficacious for its intended use, and to determine warnings, precautions, and adverse reactions that are associated with such product in the dosage range to be prescribed, which trial is intended to support Regulatory Approval of such product, as described in 21 C.F.R. 312.21(c). 1.185. [***] 1.186. [***]