Research limitations Sample Clauses

Research limitations. The research concentrates only on four Finnish nearby suppliers because the very spe- cific information is considered to be most important in this thesis. In this case confiden- tial face to face interviews are the best way to get this information. It would be great to include more supply companies to this thesis but because of nature of the interviews it would require more time and recourses to conduct that kind of a study. Hopefully findings from this thesis will give useful information to the case com- pany but also to future researches to dig even more deeper on this subject. It is known that there are researches studying supplier cooperation but most of those are done for large amount of companies by structured interviews in which answers are given for example by scale from one to five like in Likert scale. In those studies, there is no possibility to give any detailed explanations to answers. The analysis is done based on the answers from interviews of supply companies intro- duced in this thesis and the literature reviewed. Information is very important to case company but also some suggestions can be made on more general level. Also, it has to be remembered that there are cultural differences in cooperation between countries. So, in this case findings are best relevant in Finland, but it would be great to compare this kind of researches from different countries.
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Research limitations. 非經乙方事前書面同意,於本研究之研究期間內,甲方、計畫主持人與共同主持人及甲方參與本研究之人員不得為第三人從事與本研究內容相同之工作。 During the research period of this Research, without the prior written consent of Party B, Party A, the PI, the Co-PI, and personnel participating in this Research may not engage in work similar to the content of this Research for any third party. 第18條. 權利義務轉讓
Research limitations. 1. This research on intercultural premarital couples counseling initially set out to examine at least eight couples, four couples who were currently in premarital counseling and four who are now married but previously received premarital counseling. However, I was unable to find eight couples and had to select the four couples that responded. 2. I also wanted to interview three therapists currently engaged in intercultural premarital couples counseling with at least one year experience. Despite my best efforts I was unable to find a therapist who had counseled intercultural couples. 3. The research was limited to participants currently living in Georgia only. 4. The participants had to be well versed in written and spoken English. 5. A particular limitation was not set for a given ethnicity or cultural background. The research had to be left open as the researcher was unsure of who will respond to the request to participate in the research. As a result the research content turned out to be more general than specific. 6. The current research does not seek to analyze any particular theory or theorist or programs but seeks to examine integrated approaches that may be helpful in intercultural premarital couples counseling.
Research limitations. Perhaps the largest limitation in the research is the inability to develop a framework which is useful to all provider types and practice sizes. Given the wide variation in organization size, services provided and analytic capability, it is difficult to develop a framework that is feasible across all care settings. However, it is anticipated that any provider who services a diabetic population will find at least one component of the current framework useful for evaluation purposes. For instance, even if a provider does not have a patient portal, at a minimum, the practice could implement the XXX and target those patients who have low scores to encourage use of EHR or other activities to increase engagement. Ideally, however, a provider will have a patient portal and the capability to capture some of the proposed metrics. Further, the proposed methodology, a quasi-experimental study design, which includes both intervention and comparison groups, may not be feasible for all providers. This type of study requires dedicated resources to implement, manage and report on the evaluation. Selection bias is also an issue with this study since the intervention group is not selected randomly and because participants are self-selected into the study by their enrollment in the patient portal. Other studies have also found that portal users may differ from non-portal users in other ways that may introduce additional bias. Tenforde, et al found that compared to non-users, PHR users were younger, had higher incomes and educational attainment, were more likely to identify as Caucasian, and had better unadjusted and adjusted diabetes quality measure profiles (Tenforde, 2012). These differences may have the potential to skew some of the evaluation results although this can be mitigated some by controlling for these variables in analysis. As a growing number of providers transition to electronic health records, understanding the impact of these public health informatics systems is critical. Research that identifies how to increase patient engagement through the EHR may have substantial benefit for public health practitioners. By understanding the relationships between use of the patient portal features available in the EHR and how these play a role increasing patient engagement and health outcomes, practitioners can provide better quality services. While the main focus of this thesis is the role of technology and the patient to increase engagement and improve health outcomes, ...
Research limitations. During the research period of this Research, without the prior written consent of Party B, Party A, the PI, the Co-PI, and personnel participating in this Research may not engage in work similar to the content of this Research for any third party.

Related to Research limitations

  • Research Collaboration 3.7.1 Aarvik shall carry out the activities of each Work Item and deliver the required Data Package and/or deliverables in accordance with the applicable SOW. Without limiting the generality of the foregoing, Aarvik shall, in accordance with the applicable SOWs and the timeline approved by JRC, apply the Aarvik IP to (i) design and synthesize Collaboration Compounds, and (ii) by itself or through subcontractor(s), [***]. During the Research Term, if any Party identifies any Third Party Patent or Know-How that is necessary or reasonably useful for any activity under the SOWs but has not been included in the Aarvik IP, then such Party shall immediately inform the other Party and the Parties shall discuss in good faith the need of obtaining a license from such Third Party. 3.7.2 No later than [***] ([***]) days after completion of the [***], Aarvik shall, to the extent not already provided to ArriVent, deliver the Data Packages and all other deliverables required under the [***], as well as the results of the Patentability and FTO Analysis as described in Section 3.2.3, to ArriVent. ArriVent shall have the sole discretion to decide whether or not to advance any Collaboration Compound and which Collaboration Compound(s) will be advanced for further studies beyond the [***]. ArriVent shall inform Axxxxx of its decision in writing. If AxxxXxxx decides to advance the Collaboration Program to [***], ArriVent shall make the payment for the [***] pursuant to Section 6.2.1. 3.7.3 If, upon completion of the [***] for the Collaboration Program, AxxxXxxx decides not to advance the Collaboration Program to [***], ArriVent may terminate the Collaboration Program. If AxxxXxxx decides to advance the Collaboration Program to [***], ArriVent shall make the payment for the [***] pursuant to Section 6.2.1. 3.7.4 No later than [***] ([***]) days after completion of the [***], Aarvik shall, to the extent not already provided to ArriVent, deliver all Data Packages and deliverables required under the [***] to ArriVent. ArriVent shall have the sole discretion to decide whether or not to advance any Collaboration Compound and which Collaboration Compound(s) will be advanced for further studies beyond the [***]. ArriVent shall inform Axxxxx of its decision in writing. 3.7.5 No later than [***] ([***]) days after completion of the [***], Aarvik shall, to the extent not already provided to ArriVent, deliver all Data Packages and deliverables required under the [***] to ArriVent. 3.7.6 Within [***] ([***]) days after completion of the [***], Aarvik shall deliver to ArriVent a full report on all key results and findings of the Collaboration Program, and such other data, results and information as ArriVent may deem necessary for it to determine whether or not to exercise the Option (the “Full Report”).

  • Research Use The Requester agrees that if access is approved, (1) the PI named in the DAR and (2) those named in the “Senior/Key Person Profile” section of the DAR, including the Information Technology Director and any trainee, employee, or contractor1 working on the proposed research project under the direct oversight of these individuals, shall become Approved Users of the requested dataset(s). Research use will occur solely in connection with the approved research project described in the DAR, which includes a 1-2 paragraph description of the proposed research (i.e., a Research Use Statement). Investigators interested in using Cloud Computing for data storage and analysis must request permission to use Cloud Computing in the DAR and identify the Cloud Service Provider (CSP) or providers and/or Private Cloud System (PCS) that they propose to use. They must also submit a Cloud Computing Use Statement as part of the DAR that describes the type of service and how it will be used to carry out the proposed research as described in the Research Use Statement. If the Approved Users plan to collaborate with investigators outside the Requester, the investigators at each external site must submit an independent DAR using the same project title and Research Use Statement, and if using the cloud, Cloud Computing Use Statement. New uses of these data outside those described in the DAR will require submission of a new DAR; modifications to the research project will require submission of an amendment to this application (e.g., adding or deleting Requester Collaborators from the Requester, adding datasets to an approved project). Access to the requested dataset(s) is granted for a period of one (1) year, with the option to renew access or close-out a project at the end of that year. Submitting Investigator(s), or their collaborators, who provided the data or samples used to generate controlled-access datasets subject to the NIH GDS Policy and who have Institutional Review Board (IRB) approval and who meet any other study specific terms of access, are exempt from the limitation on the scope of the research use as defined in the DAR.

  • Patentable Inventions or Discoveries Any inventions or discoveries developed in the course, or as a result, of services in connection with the Contract that are patentable pursuant to 35 U.S.C. § 101 are the sole property of the State of Florida. Contractor must inform the Customer of any inventions or discoveries developed or made through performance of the Contract, and such inventions or discoveries will be referred to the Florida Department of State for a determination on whether patent protection will be sought. The State of Florida will be the sole owner of all patents resulting from any invention or discovery made through performance of the Contract.

  • Research Matters By entering into this Agreement, the Placement Agent does not provide any promise, either explicitly or implicitly, of favorable or continued research coverage of the Company and the Company hereby acknowledges and agrees that the Placement Agent’s selection as a placement agent for the Offering was in no way conditioned, explicitly or implicitly, on the Placement Agent providing favorable or any research coverage of the Company. In accordance with FINRA Rule 2711(e), the parties acknowledge and agree that the Placement Agent has not directly or indirectly offered favorable research, a specific rating or a specific price target, or threatened to change research, a rating or a price target, to the Company or inducement for the receipt of business or compensation.

  • Research Primary Investigator as part of a multi-site study (25 points) • Co-Investigator as part of a multi-site study (20 points) • Primary Investigator of a facility/unit based research study (15 points) • Co-Investigator of a facility/unit based research study (10 points) • Develops a unit specific research proposal (5 points) • Conducts a literature review as part of a research study (5 points)

  • Scope of Collaboration As part of the collaboration, the Controllers will act as Joint Controller. The roles of the Controller and the associated tasks are specified in more detail in Appendix 1. If one party is solely responsible for a data processing operation, this party will implement all relevant data protection provisions on its own responsibility. However, such data processing procedures are not subject to this Agreement. Joint data processing and the type of Personal Data collected and processed within the framework of collaboration are specified in Appendix 1.

  • Research Program The term “Research Program” shall mean the research program to be undertaken by TSRI under the direction and control of the Principal Investigator as expressly set forth on Exhibit A hereto.

  • Joint Inventions For Subject Inventions conceived or first actually reduced to practice under this Agreement that are joint Subject Inventions made by CONTRACTOR and USER, each Party shall have the option to elect and retain title to its undivided rights in such joint Subject Inventions.

  • Research Term The term “

  • Research Plan The Parties recognize that the Research Plan describes the collaborative research and development activities they will undertake and that interim research goals set forth in the Research Plan are good faith guidelines. Should events occur that require modification of these goals, then by mutual agreement the Parties can modify them through an amendment, according to Paragraph 13.6.

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