Profile of the participants to the focus group interviews
Participant | Age | Gender | Occupation | Use of the OFODSs during the 2020 year (range of times) | |||
---|---|---|---|---|---|---|---|
20–30 | 31–40 | 41–50 | >50 | ||||
P1 | 56 | Female | Self-employed | ✗ | |||
P2 | 59 | Male | Self-employed | ✗ | |||
P3 | 60 | Male | Self-employed | ✗ | |||
P4 | 57 | Female | Employee worker | ✗ | |||
P5 | 75 | Female | Retired | ✗ | |||
P6 | 56 | Female | Self-employed | ✗ | |||
P7 | 66 | Female | Self-employed | ✗ | |||
P8 | 50 | Male | Self-employed | ✗ | |||
P9 | 43 | Female | Employee worker | ✗ | |||
P10 | 44 | Female | Employee worker | ✗ | |||
P11 | 46 | Female | Employee worker | ✗ | |||
P12 | 43 | Female | Employee worker | ✗ | |||
P13 | 53 | Female | Self-employed | ✗ | |||
P14 | 48 | Female | Employee worker | ✗ | |||
P15 | 26 | Male | Employee worker | ✗ | |||
P16 | 40 | Male | Self-employed | ✗ | |||
P17 | 32 | Female | Employee worker | ✗ | |||
P18 | 26 | Male | Employee worker | ✗ | |||
P19 | 30 | Male | Employee worker | ✗ | |||
P20 | 26 | Female | Employee worker | ✗ | |||
P21 | 23 | Male | Employee worker | ✗ | |||
P22 | 19 | Female | Student | ✗ | |||
P23 | 20 | Female | Student | ✗ | |||
P24 | 19 | Female | Student | ✗ | |||
P25 | 23 | Female | Student | ✗ | |||
P26 | 23 | Female | Employee worker | ✗ | |||
P27 | 19 | Male | Student | ✗ | |||
P28 | 45 | Male | Self-employed | ✗ | |||
P29 | 70 | Male | Retired | ✗ | |||
P30 | 26 | Male | Employee worker | ✗ |
Types of expectations about OFODS quality
Dimension of customer expectations | Category of expectations | Types of expectations | Frequency |
---|---|---|---|
Punctuality of delivery | 30 | ||
Accuracy of delivery | 30 | ||
Quality of the delivered product | 27 | ||
Appropriateness of the fee applied for the online purchase | 25 | ||
Compliance with hygiene and safety regulations | 25 | ||
Professionalism, empathy and kindness of service provider | 24 | ||
Multichannel service | 26 | ||
Product and delivery customised | 24 | ||
Payment service | 22 | ||
Information about the service | 25 | ||
After-sales contact | 17 | ||
Availability and variety of the offer | 15 | ||
Sustainability-oriented service | 22 | ||
Skills to broaden service range | 20 |
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About the authors.
Angelo Bonfanti, Ph.D., is an associate professor of business management at the Department of Business Administration, the University of Verona (Italy). His current research interests include service management and marketing, especially hospitality and retail management, as well as social entrepreneurship. He has published articles in several journals such as Business Strategy and the Environment , European Management Journal , International Journal of Hospitality Management , International Journal of Quality and Service Sciences , International Journal of Retail and Distribution Management , Management Decision , Psychology & Marketing , and the TQM Journal .
Chiara Rossato, Ph.D., is an assistant professor of business management at the Department of Business Administration, the University of Verona (Italy). Her research interests include service management and strategic management. She has published articles in the following journals: Journal of Place Management and Development , Review of Managerial Science , the TQM Journal and Total Quality Management and Business Excellence .
Vania Vigolo, Ph.D., is an associate professor of business management at the Department of Business Administration, the University of Verona (Italy). Her research interests include tourist behavior, tourism and hospitality marketing, services marketing, and branding strategies. She has published works in several journals including International Journal of Hospitality Management , International Journal of Tourism Research , Journal of Environmental Management , Journal of Fashion Marketing and Management , Nonprofit and Voluntary Sector Quarterly , Psychology and Marketing and the TQM Journal .
Alfonso Vargas-Sánchez, Ph.D., is a full professor of strategic management at the University of Huelva (Spain), where he heads the research group on tourism, named Grupo de Investigación en Estrategias de Innovación y Desarrollo en la Empresa Turística (GEIDETUR). His current research interests include strategic management, tourism management and marketing. He has authored a number of articles published in journals such as Annals of Tourism Research , International Journal of Business Environment , International Journal of Contemporary Hospitality Management , Journal of Heritage Tourism , Journal of Hospitality Marketing and Management , Journal of Sustainable Tourism , Journal of Travel Research and Tourism Management.
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2020, International Research Journal of Modernization in Engineering Technology an d Science
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Under the PRA ( 44 U.S.C. 3501-3521 ), Federal Agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. “Collection of information” is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and includes Agency requests or requirements that members of the public submit reports, keep records, or provide information to a third party. Section 3506(c)(2)(A) of the PRA ( 44 U.S.C. 3506(c)(2)(A) ) requires Federal Agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, before submitting the collection to OMB for approval. To comply with this requirement, FDA is publishing notice of the proposed collection of information set forth in this document.
With respect to the following collection of information, FDA invites comments on these topics: (1) whether the proposed collection of information is necessary for the proper performance of FDA's functions, including whether the information will have practical utility; (2) the accuracy of FDA's estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques, when appropriate, and other forms of information technology.
This information collection helps support implementation of sections 503A and 503B of the Federal Food, Drug, and Cosmetic Act (FD&C Act) ( 21 U.S.C. 353a and 21 U.S.C. 353b ), which govern compounding by pharmacies, outsourcing facilities, and other entities. Compounding is generally a practice in which a licensed pharmacist, a licensed physician, or, in the case of an outsourcing facility, a person under the supervision of a licensed pharmacist, combines, mixes, or alters ingredients of a drug to create a medication tailored to the needs of an individual patient. Although compounded drugs can serve an important medical need for certain patients, they also present risks to patients. FDA's compounding program aims to protect patients from unsafe, ineffective, and poor-quality compounded drugs, while preserving access to lawfully marketed compounded drugs for patients who have a medical need for them. Respondents to the information collection are pharmacies, outsourcing facilities, and other entities.
To assist respondents in complying with statutory requirements, we have issued the following topic-specific guidance documents:
Title | Notice of availability publication date |
---|---|
Compounding and Repackaging of Radiopharmaceuticals by State-Licensed Nuclear Pharmacies, Federal Facilities, and Certain Other Entities (Radiopharmaceutical Compounding and Repackaging Guidance) (available at ) | September 26, 2018 ( ). |
Compounding and Repackaging of Radiopharmaceuticals by Outsourcing Facilities (Radiopharmaceutical Compounding and Repackaging by Outsourcing Facilities Guidance) (available at ) | September 26, 2018 ( ). |
Repackaging of Certain Human Drug Products by Pharmacies and Outsourcing Facilities (Repackaging Guidance) (available at ) | January 13, 2017 ( ). |
Mixing, Diluting, or Repackaging Biological Products Outside the Scope of an Approved Biologics License Application (Biological Products Guidance) (available at ) | January 19, 2018 ( ). |
These guidance documents were issued consistent with FDA's good guidance practice regulations in 21 CFR 10.115 , which provide for public comment at any time. The guidance documents communicate FDA's current thinking on the respective topics and include information collection that may result in expenditures of time and effort by respondents. In FDA's notices of availability for the guidance documents, we also solicited public comment under the PRA on the information collection provisions. FDA has developed and maintains a searchable guidance database available at https://www.fda.gov/regulatory-information/search-fda-guidance-documents . Guidance documents covered by this information collection may be found by choosing “Center for Drug Evaluation and Research” from among the FDA Organizations, and by selecting the term Start Printed Page 49882 “Compounding” from among the possible Filters. [ 1 ]
Because Congress explicitly excluded radiopharmaceuticals from section 503A of the FD&C Act (see section 503A(d)(2)), compounded radiopharmaceuticals are not eligible for the exemptions under section 503A from section 505 of the FD&C Act ( 21 U.S.C. 355 ) (concerning new drug approval requirements), section 502(f)(1) of the FD&C Act ( 21 U.S.C. 352(f)(1) ) (concerning labeling with adequate directions for use), and section 501(a)(2)(B) of the FD&C Act ( 21 U.S.C. 351(a)(2) B)) (concerning current good manufacturing practice (CGMP) requirements). In addition, the FD&C Act does not provide an exemption for repackaged radiopharmaceuticals. The guidance describes the conditions under which FDA does not intend to take action for violations of sections 505, 502(f)(1), and 501(a)(2)(B) of the FD&C Act when a State-licensed nuclear pharmacy, Federal facility, or other facility that is not an outsourcing facility and that holds a radioactive materials license for medical use issued by the Nuclear Regulatory Commission or by an Agreement State compounds or repackages radiopharmaceuticals for human use. The guidance explains that one condition is that the compounded radiopharmaceutical is not essentially a copy of an approved radiopharmaceutical. As described in the guidance, FDA does not intend to consider a compounded radiopharmaceutical to be essentially a copy if, among other reasons, there is a change between the compounded radiopharmaceutical and the approved radiopharmaceutical that produces a clinical difference for an identified individual patient, as determined by the prescribing practitioner and documented in writing on the prescription or order. In addition, FDA does not intend to consider a compounded radiopharmaceutical to be essentially a copy if the FDA-approved radiopharmaceutical is on FDA's drug shortage list (see section 506E of the FD&C Act ( 21 U.S.C. 356e )) at the time of compounding and distribution. If the facility compounded a drug that is identical or nearly identical to an approved drug product that appeared on FDA's drug shortage list, the facility should maintain documentation ( e.g., a notation on the order for the compounded drug) regarding the status of the drug on FDA's drug shortage list at the time of compounding, distribution, and dispensing.
In contrast to section 503A, section 503B of the FD&C Act does not exclude radiopharmaceuticals. Therefore, FDA's overall policies regarding section 503B of the FD&C Act apply to the compounding of radiopharmaceuticals. However, we have developed specific policies that apply only to the compounding of radiopharmaceuticals by outsourcing facilities using bulk drug substances and to the compounding of radiopharmaceuticals by outsourcing facilities that are essentially copies of approved drugs when such compounding is limited to minor deviations, as that term is defined in the guidance. FDA issued this guidance in part to describe the conditions under which the Agency does not generally intend to take action for violations of sections 505 and 502(f)(1) of the FD&C Act when an outsourcing facility repackages radiopharmaceuticals for human use.
As discussed in the guidance, one condition is that if a radiopharmaceutical is repackaged by an outsourcing facility, the label on the immediate container (primary packaging, e.g., the syringe) of the repackaged product includes certain information.
The guidance describes the conditions under which FDA does not intend to take action for violations of sections 505 (concerning new drug applications), 502(f)(1) (concerning labeling with adequate directions for use), 582 (( 21 U.S.C. 360eee-1 ) concerning drug supply chain security requirements), and (where specified in the guidance) 501(a)(2)(B) of the FD&C Act (concerning CGMPs), when a State-licensed pharmacy, Federal facility, or outsourcing facility repackages certain prescription drugs. One condition discussed in the guidance is that if a drug is repackaged by an outsourcing facility, the label on the immediate container (primary packaging, e.g., the syringe) of the repackaged product includes certain information described in the guidance.
Conditions discussed in the guidance include that if a drug is repackaged by an outsourcing facility, the label on the immediate container (primary packaging, e.g., the syringe) and on the container from which the individual units are removed for administration (secondary packaging, e.g., the bag, box, or other package in which the repackaged products are distributed) of the repackaged product include certain information described in the guidance.
Certain licensed biological products may sometimes be mixed, diluted, or repackaged in a way not described in the approved labeling for the product to meet the needs of a specific patient. As described in the guidance, biological products subject to licensure under section 351 of the Public Health Service (PHS) Act ( 42 U.S.C. 262 ) are not eligible for the statutory exemptions available to certain compounded drugs under sections 503A and 503B of the FD&C Act. In addition, a biological product that is mixed, diluted, or repackaged outside the scope of an approved biologics license application (BLA) is considered an unlicensed biological product under section 351 of the PHS Act.
This guidance document describes several conditions under which FDA does not intend to take action for violations of section 351 of the PHS Act and sections 502(f)(1), 582, and (where specified) 501(a)(2)(B) of the FD&C Act, when a State-licensed pharmacy, a Federal facility, or an outsourcing facility dilutes, mixes, or repackages certain biological products outside the scope of an approved BLA.
One condition discussed in the guidance is that if the labeling for the licensed biological product includes storage instructions, handling instructions, or both ( e.g., protect from light, do not freeze, keep at specified storage temperature), the labeling for the biological product that is mixed, diluted, or repackaged specifies the same storage conditions. Another condition described in the guidance is that, if the biological product is mixed, diluted, or repackaged by an outsourcing facility, the label on the immediate container (primary packaging, e.g., the syringe) of the mixed, diluted, or repackaged product includes certain information described in the guidance. In addition, the guidance communicates that as a condition for biological products mixed, diluted, or repackaged by an outsourcing facility that, if the immediate product label is too small to bear the active and inactive ingredients, such information is included on the label of the container from which the Start Printed Page 49883 individual units are removed for administration (secondary packaging, e.g., the bag, box, or other package in which the mixed, diluted, or repackaged biological products are distributed).
The guidance also communicates FDA's thinking about the condition for biological products mixed, diluted, or repackaged by an outsourcing facility that the label on the container from which the individual units are removed for administration include directions for use. These directions include, as appropriate, the dosage and administration and the following information to facilitate adverse event reporting: https://www.fda.gov/medwatch and 1-800-FDA-1088.
Finally, another condition described in the guidance is that outsourcing facilities maintain records of the testing performed in accordance with “Appendix A—Assigning a BUD for Repackaged Biological Products Based on Stability Testing” of the guidance for biological products repackaged by outsourcing facilities for which the beyond use date (BUD) is established based on a stability program conducted in accordance with Appendix A.
Section III.C of the guidance, “Licensed Allergenic Extracts for Subcutaneous Immunotherapy,” discusses the preparation of prescription sets ( i.e., licensed allergenic extracts that are mixed and diluted to provide subcutaneous immunotherapy to an individual patient) by a physician, a State-licensed pharmacy, a Federal facility, or an outsourcing facility. Another condition described in the guidance is that if the prescription set is prepared by an outsourcing facility, the label of the container from which the individual units of the prescription set are removed for administration (secondary packaging) includes the following information to facilitate adverse event reporting: https://www.fda.gov/medwatch and 1-800-FDA-1088. Each prescription set prepared by an outsourcing facility is also accompanied by instructions for use.
Outsourcing facilities submit their initial and biannual product reports identifying drug products repackaged during the previous 6-month period to FDA via the Agency's electronic Drug Registration and Listing System (eDRLS) as explained in the Radiopharmaceutical Compounding and Repackaging Guidance by Outsourcing Facilities and the Repackaging Guidance. Also, we expect to receive no waiver requests from the electronic submission process for initial product reports and semiannual reports.
We estimate the burden of this information collection as follows:
Recommended activity; guidance section | Number of recordkeepers | Number of records per recordkeeper | Total annual records | Average burden per recordkeeping | Total hours |
---|---|---|---|---|---|
Consultation between the compounder and prescriber and the notation on the prescription or order documenting the prescriber's determination of clinical difference (section III.A of the Radiopharmaceutical Compounding and Repackaging Guidance) | 10 | 25 | 250 | .05 (3 minutes) | 12.5 |
Maintaining records of testing performed in accordance with Appendix A of the Biological Products Guidance (section III.B of the Biological Products Guidance) | 5 | 30 | 150 | 0.083 (5 minutes) | 12.5 |
Total | 15 | 400 | 25 | ||
There are no capital costs or operating and maintenance costs associated with this collection of information. |
Recommended activity; guidance section | Number of respondents | Number of disclosures per respondent | Total annual disclosures | Average burden per disclosure | Total hours |
---|---|---|---|---|---|
Designing, testing, and producing each label on immediate containers, packages, and/or outer containers (section III.B of the Radiopharmaceutical Compounding and Repackaging Guidance by Outsourcing Facilities) | 2 | 5 | 10 | 0.5 (30 minutes) | 5 |
Designing, testing, and producing each label on immediate containers, packages, and/or outer containers (section III.A of the Repackaging Guidance) | 6 | 36 | 216 | 1 | 216 |
Designing, testing, and producing the label, container, packages, and/or outer containers for each mixed, diluted, or repackaged biological product (section III.B of the Biological Products Guidance) | 15 | 5 | 75 | 0.5 (30 minutes) | 37.5 |
Designing, testing, and producing each label on immediate containers, packages, and/or outer containers for each licensed allergenic extract (section III.C of the Biological Products Guidance) | 5 | 300 | 1,500 | 0.5 (30 minutes) | 750 |
Total | 28 | 1,801 | 1,009 | ||
There are no capital costs or operating and maintenance costs associated with this collection of information. | |||||
Totals may not sum due to rounding. |
Recommended activity; guidance section | Number of respondents | Number of disclosures per respondent | Total annual disclosures | Average burden per disclosure | Total hours |
---|---|---|---|---|---|
Biannual product reports identifying drug products repackaged by the outsourcing facility during the previous 6-month period (section III.B of the Radiopharmaceutical Compounding and Repackaging Guidance by Outsourcing Facilities) | 2 | 2 | 4 | 3 | 12 |
Biannual product reports identifying drug products repackaged by the outsourcing facility during the previous 6-month period (section III.A of the Repackaging Guidance) | 6 | 2 | 12 | 3 | 36 |
Total | 8 | 16 | 48 | ||
There are no capital costs or operating and maintenance costs associated with this collection of information. |
For purposes of our analysis, we characterize the burden associated with the time and effort expended on the information collection recommendations discussed in the respective guidance documents as either recordkeeping, reporting, or third-party disclosure activities. We reconfigured the original table by splitting it into three tables to better differentiate between the estimated annual recordkeeping burden, the estimated annual reporting burden, and the estimated annual third-party disclosure burden. At the same time, our findings show that compliance with recordkeeping requirements applicable to compounded and repackaged drug products is standard practice in the compounding and selling of these drug products under States' pharmacy laws and other State laws governing recordkeeping by healthcare professionals and healthcare facilities. Therefore, we excluded from our estimate recordkeeping practices discussed in the respective guidance documents we consider usual and customary. We invite comment on this assumption.
For the Repackaging Guidance, to correct a clerical error, we have adjusted the number of disclosures per respondent from 21 to 36 because each respondent is estimated to average 6 different products and average 6 different strengths, which requires 36 (6 × 6) unique labels per respondent. The initial narrative reflected that each product would come in 6 different strengths and thus require 6 unique labels, but due to a clerical error, this information was not correctly included in the table. We also adjusted the number of respondents to 6 to match the number of respondents designing, testing, and producing labels. In addition, we adjusted the total number of disclosures per respondent to 2 given the biannual reporting requirement.
For the Radiopharmaceutical Compounding and Repackaging by Outsourcing Facilities Guidance, a row for biannual product reporting was added to capture product reporting that was inadvertently omitted.
Our estimated burden for the information collection reflects constant respondent numbers. The original numbers were based on the information the program received from product reporting data. We do not have a mechanism in place to determine whether or not these numbers have fluctuated upward or downward; however, based on analogous observations of industry through program experience (some product reports), we believe these numbers are constant. Repackagers who are also registered as outsourcing facilities (OF) are not entity types that are individually regulated as repackagers. They are subsumed in the OF entity type and not easily distinguishable. They may or may not report their repackaging operations.
We are updating the information collection to include burden attendant to reporting and disclosure recommendations found in the Agency guidance documents that was inadvertently omitted in the original information collection due to clerical errors. The burden estimate is adjusted to reflect a resulting increase of 114 hours and 94 responses annually.
Dated: June 6, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
1. Guidance documents applicable to animal drug compounding regulated by the Center for Veterinary Medicine would also be returned if no FDA Organization is selected; this information collection covers only those compounding guidance documents issued by the Center for Drug Evaluation and Research and Center for Biologics Evaluation and Research.
[ FR Doc. 2024-12783 Filed 6-11-24; 8:45 am]
BILLING CODE 4164-01-P
Information.
IMAGES
COMMENTS
This study looked at some of these small e-commerce food businesses in the Philippine setting, in order to understand their operational structures, strategies and challenges,
1. Introduction. Retailing is a distribution process of a retailer by procuring goods and services from a distributor and selling it in small lots to a large number of customers. According to Dawson (2010), food retailing is a highly innovative sector within the entire food chain.
During the global 2020 COVID-19 outbreak, the advantages of online food delivery (FD) were obvious, as it facilitated consumer access to prepared meals and enabled food providers to keep operating.
COVID-19 pandemic shifted the conventional kind of food service to online processing and delivery of food to consumers. (Garceau, 2020). The online food delivery service made its significant mark during the beginning of the global pandemic, it is the foremost savior of the food industry (Gamilla, 2021) Existing research studies on food
Despite the popularity of online food delivery systems in the foodservice industry, there have been few studies into customers' decision-making process to use online food delivery services during the Coronavirus disease (COVID-19) pandemic. This study applied the technology acceptance model (TAM) to examine the factors affecting customers' intention to use online food delivery services ...
The focus of this study is to determine the level of customer satisfaction towards food delivery services. This research is anchored on McCarthy’s 4P’s theory or the Marketing Mix, the Product, Price, Place, and Promotion. This study used the descriptive method. The study revealed that the service delivery of the walk-in and ...
Background Food prepared out-of-home is typically energy-dense and nutrient-poor. This food can be purchased from multiple types of retailer, including restaurants and takeaway food outlets. Using online food delivery services to purchase food prepared out-of-home is increasing in popularity. This may lead to more frequent unhealthy food consumption, which is positively associated with poor ...
Online food delivery has emerged as a popular trend in e-commerce space, and serves as a tool to reach a larger number of consumers in a cost effective manner (Ray et al., 2019). Online food delivery (OFD) refers to online channel that consumers use to order food from restaurants and fast-food retailers (Elvandari et al., 2018).
Lockdown measures brought about by the COVID-19 pandemic have notably shifted food purchasing behavior towards online food delivery services (OFDS). This study examined consumer satisfaction with OFDS and their relationship to food choice and frequency of use among 18-24-year-old University of the Philippines Los Baños (UPLB) students. Through a survey of 80 students who used […]
Food businesses benefit from an online food ordering and delivery framework. The purpose of this study is to identify the factors that influence overall consumer satisfaction with online food delivery providers. The demographic information of the respondents was discussed in this study. Furthermore, this study also revealed a significant difference between respondents' perceptions of e ...
HIGHLIGHTS• Assess the Grabfood delivery rider's services and determine its effect on customer satisfaction based on the customer's perception in Cebu City.• Problem discussion describing the importance of studying the service quality of online food delivery riders and its impact on customer satisfaction was discussed.•
Purpose. Online food delivery (OFD) has witnessed momentous consumer adoption in the past few years, and COVID-19, if anything, is only accelerating its growth. This paper captures numerous intricate issues arising from the complex relationship among the stakeholders because of the enhanced scale of the OFD business.
1. Introduction. According to global estimates from 2016, 11% of men and 15% of women were living with obesity, which has been associated with multiple co-morbidities [1,2].Whilst the drivers of obesity are complex, the role of excess calorie intake through consumption of food prepared away-from-home has been recognized in previous research [3,4,5]. ...
The food service industry was one of the essential services that were allowed to operate during the pandemic in the Philippines. The OFD statistics in the Philippines showed that there were 2·9 million users of online delivery platforms, and the largest segment is in the restaurant-to-consumer delivery service, which logged 9·3 million users.
During the global 2020 COVID-19 outbreak, the advantages of online food delivery (FD) were obvious, as it facilitated consumer access to prepared meals and enabled food providers to keep operating. However, online FD is not without its critics, with reports of consumer and restaurant boycotts. It is, therefore, time to take stock and consider the broader impacts of online FD, and what they ...
International Journal of Current Science Research and Review ISSN: 2581-8341 Volume 04 Issue 08 August 2021 ... of online food delivery businesses in Daet, Camarines Norte has 11 to 15 riders comprising of 10 respondents or 41.66 percent while ... online food delivery business is an easy service business to start with. This implies that the ...
Table 2 shows the 10 most cited research papers in the area of OFD. As such, Yeo et al ... Literature synthesis into OFD-domains presented in '3.8 Domains in online food delivery research ... Identification of technical requirement for improving quality of local online food delivery service in Yogyakarta. J. Ind. Inf. Technol. Agric., 1 (2 ...
Consumers turned to online food delivery as alternative to buy in stores and restaurants. The online food delivery is keeping the food industry alive, by trying to mitigate food business from shutting down. ... Evidence from the Philippines. International Journal of Progressive Research in Science and Engineering, 2(4), 24-26. Retrieved from ...
According to the "Online Food Delivery (OFD) Services Global Market Report 2020-2030," the OFD market is projected to grow from $107.44 billion in 2019 to $154.34 billion in 2023 (Businesswire ...
Customers who make use of online meal delivery services consider a wait of thirty minutes to be appropriate and acceptable (Figure 3). 75% of respondents think it is acceptable to have to wait 30 minutes for online food delivery. And 37% out of 1000 survey res-pondents prefer drive-through for restaurant ordering.
Chan and Gao (2021) proposed the up-to-date quality of online food delivery (DEQUAL) index using 32 validated indicators to measure the up-to-date quality of online food delivery and suggested how to improve customer satisfaction and loyalty to a restaurant. Research in the food literature has explored the effect of OFODS service quality on ...
RRL 1. Impact of Online Food Delivery on Customers Summary: Ordering food is now a convenient activity with the click of a button. Menus and recipes can be searched online without the pressure of pronouncing such difficult names. Order the food online today, for easy and fast access to the food of the customer's choice.
The popularity of online food ordering and service delivery is growing steadily; user perception is also increasing. This research paper aims to investigate consumers' views about the services they receive through different sites. This paper will help service providers identify consumer needs" and ideas on the basis of the outcome of the ...
The Food and Drug Administration (FDA, Agency, or we) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register...