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1.
F1000Res ; 13: 832, 2024.
Article in English | MEDLINE | ID: mdl-39328392

ABSTRACT

Background: Public tenders are vital for a country's GDP and citizens' quality of life, enabling public administration to achieve various goals. Developing and developed countries allocate over 10% of their GDP to public procurement. This highlights the significant societal support public tenders can provide, making it important to consider how they can further benefit society. Policy and implications: Public procurement can achieve policy objectives and benefit society by selecting tenders based on criteria beyond price, such as economic advantage and social benefits. This approach, endorsed by EU directives since 2014, encourages innovation and socially responsible practices. Contracting authorities in the EU can use social, environmental, and qualitative criteria to determine the most advantageous offers.Poland's Public Procurement Law (PPL) allows contract award criteria based on quality and price, including social aspects. Contracting authorities can specify criteria like employing marginalized groups, though these criteria often face scrutiny and legal challenges. Non-price criteria aim to enhance competition and achieve social, environmental, and economic goals. Recommendations: EU and Polish laws permit and encourage using social aspects as contract award criteria in public procurement. However, contracting authorities must analyze priorities, risk balancing, time constraints, and departmental coordination to effectively implement these criteria. This approach can improve the social situation and support specific groups. Conclusions: Public procurement significantly influences a country's economy and quality of life, with EU and Polish laws allowing social criteria in contract awards. Directive 2014/24/EU supports tenders based on economic and social benefits. Poland's PPL aligns with this, emphasizing marginalized group employment. Effective implementation fosters job creation, social integration, and improved living standards.


Subject(s)
European Union , Poland , Humans , Contracts/legislation & jurisprudence
3.
J Int Bioethique Ethique Sci ; 35(2): 63-75, 2024.
Article in French | MEDLINE | ID: mdl-39013766

ABSTRACT

After being enthusiastic, insurers are now increasingly reluctant to exploit the blockchain. The innovative technology promising a better customer relationship and a reduction in fraud associated with automated contract management seems promising. That is the reason why it is interesting to confront blockchain technology with insurance requirements. Thus, the contribution, without wanting to be exhaustive of the various difficulties generated by the blockchain, proposes to highlight some of them by targeting in turn the insurance of property, liability or even of person. The problems, mainly of a technical nature, could justify a temporary withdrawal from the insurance market in view of the advantages presented by the use of these technologies.


Subject(s)
Blockchain , Contracts , Humans , Contracts/legislation & jurisprudence , Insurance, Health/legislation & jurisprudence
4.
JAMA ; 332(8): 615-616, 2024 08 27.
Article in English | MEDLINE | ID: mdl-39083253

ABSTRACT

This Viewpoint explains the 3 trends­personal conscience, employment contracts, and laws­that challenge physicians from putting their patients first and offers ways to reverse these barriers.


Subject(s)
Conscience , Ethics, Medical , Physicians , Professionalism , Humans , Contracts/legislation & jurisprudence , Professionalism/ethics , United States , Physicians/ethics , Physicians/legislation & jurisprudence , Physicians/psychology , Employment/legislation & jurisprudence
5.
Bioethics ; 38(8): 702-708, 2024 Oct.
Article in English | MEDLINE | ID: mdl-39072828

ABSTRACT

Some feminists hold that surrogacy contracts should be unenforceable or illegal because they contribute to and perpetuate unjust gender inequalities. I argue that in developed countries, surrogacy contracts either wouldn't have these negative effects or that these effects could be mitigated via regulation. Furthermore, the existence of a regulated surrogacy market is preferable on consequentialist grounds.


Subject(s)
Contracts , Gender Equity , Surrogate Mothers , Humans , Surrogate Mothers/legislation & jurisprudence , Female , Contracts/legislation & jurisprudence , Contracts/ethics , Pregnancy , Developed Countries , Feminism
6.
Br Dent J ; 237(2): 140, 2024 Jul.
Article in English | MEDLINE | ID: mdl-39060597
8.
Radiology ; 300(3): 506-511, 2021 09.
Article in English | MEDLINE | ID: mdl-34227885

ABSTRACT

Out-of-network (OON) balance billing, commonly known as surprise billing but better described as a surprise gap in health insurance coverage, occurs when an individual with private health insurance (vs a public insurer such as Medicare) is administered unanticipated care from a physician who is not in their health plan's network. Such unexpected OON care may result in substantial out-of-pocket costs for patients. Although ending surprise billing is patient centric, patient protective, and noncontroversial, passing federal legislation was challenging given its ability to disrupt insurer-physician good-faith negotiations and thus impact in-network rates. Like past proposals, the recently passed No Surprises Act takes patients out of the middle of insurer-physician OON reimbursement disputes, limiting patients' expense to standard in-network cost-sharing amounts. The new law, based on arbitration, attempts to protect good-faith negotiations between physicians and insurance companies and encourages network contracting. Radiology practices, even those that are fully in network or that never practiced surprise billing, could nonetheless be affected. Ongoing rulemaking processes will have meaningful roles in determining how the law is made operational. Physician and stakeholder advocacy has been and will continue to be crucial to the ongoing evolution of this process. © RSNA, 2021.


Subject(s)
Insurance Coverage/economics , Insurance Coverage/legislation & jurisprudence , Insurance, Health/economics , Insurance, Health/legislation & jurisprudence , Radiology/economics , Radiology/legislation & jurisprudence , Contracts/economics , Contracts/legislation & jurisprudence , Deductibles and Coinsurance/economics , Financing, Personal/economics , Humans , Practice Management, Medical/economics , Practice Management, Medical/legislation & jurisprudence , Reimbursement Mechanisms/economics , United States
9.
Plast Reconstr Surg ; 147(4): 680e-686e, 2021 04 01.
Article in English | MEDLINE | ID: mdl-33776044

ABSTRACT

BACKGROUND: Restrictive covenants are common in contractual agreements involving physicians and need careful consideration to minimize potential conflict during the term of the contract and on physician departure from a group practice or hospital system. METHODS: A general overview of the different components of restrictive covenants is provided, including specific information related to noncompetes, nonsolicitations, and nondisclosure agreements. RESULTS: In general, states will uphold restrictive covenants if the elements of the noncompete are reasonable regarding geographic distance restrictions (e.g., <20 air miles), time restrictions (e.g., <2 years), and scope of services. However, states vary considerably in the interpretation of restrictive covenants. Other components of the contract, such as alternative dispute resolution (mediation and/or arbitration) and buy-out clauses (i.e., liquidated damages provisions), should be considered at the time the agreement is negotiated. CONCLUSIONS: States are balancing the protection of business interests with the protection of free trade. It is important that physicians seek counsel with an experienced health care attorney with respect to restrictive covenants in his or her specific state. A simple, well-written, and reasonable restrictive covenant can often help limit legal conflict and expense.


Subject(s)
Contracts/legislation & jurisprudence , Employment/legislation & jurisprudence , Physicians , Contracts/standards , Employment/standards , United States
11.
Plast Reconstr Surg ; 147(3): 761-771, 2021 03 01.
Article in English | MEDLINE | ID: mdl-33620950

ABSTRACT

BACKGROUND: Plastic surgeons have been shown to be unprepared to negotiate their first employment contracts. Previous survey studies have attempted to assess plastic surgeons' first employment contracts to outline common pitfalls in contract negotiation. With this study, the authors aim to expand these previous studies and help plastic surgeons become prepared to negotiate their employment contracts. METHODS: A seven-question, cross-sectional survey was sent to attending-level surgeon members of the California Society of Plastic Surgeons, the American Society of Plastic Surgeons, the Texas Society of Plastic Surgeons, and the American Cleft Palate-Craniofacial Association. Questions investigated plastic surgeons' first contracts. Correlations were determined using a two-sample Wilcoxon rank sum test in an attempt to link these questions with overall satisfaction. RESULTS: From the 3908 distributed surveys, 782 (20 percent) responses were collected, and 744 were included for analysis. The majority of respondents were found to join a group-centered, private practice following residency. Surprisingly, 69 percent of surgeons did not use attorney assistance when negotiating their contract. Although greater than 70 percent of respondents reported a salary of $200,000 or less, satisfaction with one's contract was most strongly correlated with a salary of greater than $300,000 (p < 0.0001). However, only 12 percent of respondent surgeons were able to secure such a salary. CONCLUSIONS: This study examined the largest, most diverse plastic surgeon cohort to date regarding surgeons' first employment contract. Although the authors' findings indicate that certain factors should be prioritized when approaching a first employment contract, they ultimately recommend that all surgeons take into account their personal priorities and attempt to proactively define their terms of employment before signing a contract.


Subject(s)
Contracts/economics , Employment/economics , Negotiating , Surgeons/psychology , Surgery, Plastic/economics , Cohort Studies , Contracts/legislation & jurisprudence , Cross-Sectional Studies , Employment/legislation & jurisprudence , Humans , Malpractice/economics , Malpractice/legislation & jurisprudence , Salaries and Fringe Benefits/economics , Salaries and Fringe Benefits/legislation & jurisprudence , Surgeons/economics , Surgeons/legislation & jurisprudence , Surgeons/statistics & numerical data , Surgery, Plastic/legislation & jurisprudence , Surveys and Questionnaires/statistics & numerical data , United States
12.
JMIR Public Health Surveill ; 6(4): e23579, 2020 12 02.
Article in English | MEDLINE | ID: mdl-33263555

ABSTRACT

BACKGROUND: Companies use brand websites as a promotional tool to engage consumers on the web, which can increase product use. Given that some products are harmful to the health of consumers, it is important for marketing associated with these products to be subject to public health surveillance. However, terms of service (TOS) governing the use of brand website content may impede such important research. OBJECTIVE: The aim of this study is to explore the TOS for brand websites with public health significance to assess possible legal and ethical challenges for conducting research on consumer product websites. METHODS: Using Statista, we purposefully constructed a sample of 15 leading American tobacco, alcohol, psychiatric pharmaceutical, fast-food, and gun brands that have associated websites. We developed and implemented a structured coding system for the TOS on these websites and coded for the presence versus absence of different types of restriction that might impact the ability to conduct research. RESULTS: All TOS stated that by accessing the website, users agreed to abide by the TOS (15/15, 100%). A total of 11 out of 15 (73%) websites had age restrictions in their TOS. All alcohol brand websites (5/15, 33%) required users to enter their age or date of birth before viewing website content. Both websites for tobacco brands (2/15, 13%) further required that users register and verify their age and identity to access any website content and agree that they use tobacco products. Only one website (1/15, 7%) allowed users to display, download, copy, distribute, and translate the website content as long as it was for personal and not commercial use. A total of 33% (5/15) of TOS unconditionally prohibited or put substantial restrictions on all of these activities and/or failed to specify if they were allowed or prohibited. Moreover, 87% (13/15) of TOS indicated that website access could be restricted at any time. A total of 73% (11/15) of websites specified that violating TOS could result in deleting user content from the website, revoking access by having the user's Internet Protocol address blocked, terminating log-in credentials, or enforcing legal action resulting in civil or criminal penalties. CONCLUSIONS: TOS create complications for public health surveillance related to e-marketing on brand websites. Recent court opinions have reduced the risk of federal criminal charges for violating TOS on public websites, but this risk remains unclear for private websites. The public health community needs to establish standards to guide and protect researchers from the possibility of legal repercussions related to such efforts.


Subject(s)
Contracts/standards , Internet/instrumentation , Access to Information/legislation & jurisprudence , Contracts/legislation & jurisprudence , Humans , Internet/legislation & jurisprudence , Marketing/methods , Marketing/statistics & numerical data
13.
Med Law Rev ; 28(4): 794-803, 2020 Dec 17.
Article in English | MEDLINE | ID: mdl-32892220

ABSTRACT

In Barclays Bank plc v Various Claimants [2020] UKSC 13, the Supreme Court rejected the claimants' argument that Barclays should be vicariously liable for the sexual assaults of a doctor hired on as a contractor to perform medical examinations on employees and job candidates at the bank. It upheld the traditional rule that a defendant is not vicariously liable for the torts of independent contractors. This commentary examines the law on liability for independent contractors and considers whether the Supreme Court decision is consistent with modern employment trends. The implications of the decision for medical law are then discussed.


Subject(s)
Employment/legislation & jurisprudence , Liability, Legal , Physicians/legislation & jurisprudence , Sex Offenses/legislation & jurisprudence , Contracts/legislation & jurisprudence , United Kingdom
15.
Med Leg J ; 88(2): 90-97, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32490743

ABSTRACT

We consider various types of litigation that may follow the Covid-19 pandemic, including: claims against National Health Service (NHS) Trusts by patients who have contracted the coronavirus (or by their bereaved families), claims by NHS staff against their employer for a failure to provide any or adequate personal protective equipment or testing, commercial claims arising from the procurement of medical supplies, the potential liabilities to those who suffer adverse reactions to any vaccine and the guidance issued by the regulators in relation to subsequent disciplinary action.


Subject(s)
Betacoronavirus , Coronavirus Infections/epidemiology , Liability, Legal , Pneumonia, Viral/epidemiology , COVID-19 , Contracts/legislation & jurisprudence , Disease Transmission, Infectious/legislation & jurisprudence , Employee Discipline/legislation & jurisprudence , Employment/legislation & jurisprudence , Health Personnel , Humans , Malpractice/legislation & jurisprudence , Occupational Exposure/legislation & jurisprudence , Pandemics , SARS-CoV-2 , United Kingdom/epidemiology , Vaccination/legislation & jurisprudence
16.
J Med Chem ; 63(20): 11362-11367, 2020 10 22.
Article in English | MEDLINE | ID: mdl-32479727

ABSTRACT

Outsourcing has become an integral part of how research and early development (R&D) is executed in biotech companies and large pharmaceutical organizations. Drug discovery organizations can choose from several operational models when partnering with a service provider, ranging from short-term, fee-for-service (FFS)-based arrangements to more strategic full-time-equivalent (FTE)-based collaborations and even risk-sharing relationships. Clients should consider a number of criteria when deciding which contract research organization (CRO) is best positioned to help meet their goals. Besides cost, other factors such as intellectual property protection, problem solving skills, value-creation ability, communication, data integrity, safety and personnel policies, ease of communication, geography, duration of engagement, scalability of capacity, and contractual details deserve proper consideration. In the end, the success of a drug discovery partnership will depend in large part on the people who execute the science.


Subject(s)
Drug Discovery/organization & administration , Models, Organizational , Outsourced Services/organization & administration , Pharmaceutical Research/organization & administration , Contracts/economics , Contracts/legislation & jurisprudence , Cooperative Behavior , Drug Discovery/economics , Drug Discovery/legislation & jurisprudence , Efficiency, Organizational , Intellectual Property , Outsourced Services/economics , Outsourced Services/legislation & jurisprudence , Pharmaceutical Research/economics , Pharmaceutical Research/legislation & jurisprudence
17.
Acta bioeth ; 26(1): 29-36, mayo 2020.
Article in Spanish | LILACS | ID: biblio-1114595

ABSTRACT

La declaratoria del estado de emergencia, a causa de la pandemia de la covid-19, exige un análisis de la vigencia de las relaciones contractuales y cómo estas pueden verse afectadas por eventos extraordinarios, imprevisibles e irresistibles que impidan el cumplimiento de las prestaciones, así como aquellos casos en los que la alteración de las circunstancias puede llevar a que una de las partes exija al juez recomponga el contenido de la prestación pactada o la resolución del contrato.


The declaration of a state of emergency due to the covid-19 pandemic requires an analysis of the validity of the contractual relations and how these may be affected by extraordinary, unforeseeable and irresistible events that prevent the performance of the services, as well as those cases in which the alteration of circumstances may lead one of the parties to demand that the judge recompose the content of the agreed service or terminate the contract.


A declaração de estado de emergência, devido à pandemia da covid-19, exige uma análise da vigência das relações contratuais e como estas podem ser afetadas por eventos extraordinários, imprevisíveis e irresistíveis que impeçam o cumprimento das prestações, assim como aqueles casos em que a alteração das circunstâncias podem levar a que uma das partes exija que o juiz recomponha o conteúdo da prestação acordada ou a rescisão do contrato.


Subject(s)
Quarantine/legislation & jurisprudence , Coronavirus Infections , Delivery of Health Care/legislation & jurisprudence , Contracts/legislation & jurisprudence , Pandemics/legislation & jurisprudence , Peru , Pneumonia, Viral , Quarantine/ethics , Contract Liability , Delivery of Health Care/ethics , Contracts/ethics , Pandemics/ethics , Betacoronavirus
18.
J Bioeth Inq ; 17(1): 121-131, 2020 Mar.
Article in English | MEDLINE | ID: mdl-32040832

ABSTRACT

Disputes between separated couples over whether frozen embryos can be used in an attempt to create a child create a moral dilemma for public policy. When a couple create embryos intending to parent any resulting children, New Zealand's current policy requires the consent of both people at every stage of the ART process. New Zealand's Advisory Committee on Assisted Reproductive Technology has proposed a policy change that would give ex-partners involved in an embryo dispute twelve months to come to an agreement before the embryos are destroyed. New Zealand's current policy and the proposed policy both favour the person who wishes to avoid procreation. Two alternative policy approaches that do not favour procreative avoidance are considered. Using pre-fertilisation contracts to determine the decision reached in embryo disputes allows the couple's wishes at the time the embryos are created to determine what happens to the embryos if they separate. However, pre-fertilisation contracts are agreements about healthcare and personal relationships, and changing circumstances can make enforcing such agreements unjust. Finally, it is argued that New Zealand's Family Court system should be used to reach decisions that balance the interests of those involved in the dispute.


Subject(s)
Cryopreservation , Dissent and Disputes/legislation & jurisprudence , Embryo Disposition/legislation & jurisprudence , Embryo, Mammalian , Advisory Committees , Contracts/legislation & jurisprudence , Female , Humans , Male , New Zealand , Parents , Policy Making
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