Akash Sharma, M.K. Tripathi, Riya Mishra, D. K. Payasi, Ankit Pandey, Sanjeev Sharma, Nishi Mishra, Shrankhla Mishra, Shagun Nehra, Jyoti Singh & Niraj Tripathi·International Journal of Environment and Climate Change·2025
Soybean‘s productivity is severely constrained by drought stress, particularly in rainfed agro-ecosystems, leading to significant yield reductions. Thus, the present investigation was conducted to identify drought-tolerant soybean genotypes based on a comprehensive evaluation of...
Open access
Research Article10.9734/ijecc/2025/v15i115112
Aims: Himachal Pradesh is situated in the western Himalayas. Kangra district of the state, especially Shivalik hills are known to retain a rich treasure of climatic variability, favourable for diversified vegetation and insect fauna. This study assessed the abundance and diversit...
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Research Article10.9734/jabb/2025/v28i92858
This review presents a detailed comparative analysis of electron beam (e-beam) and gamma radiation sterilization technologies, with a focus on their efficacy, safety, and economic viability. Both sterilization techniques are extensively employed across medical, pharmaceutical, an...
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Research Article10.9734/mrji/2024/v34i91479
Background: This research delves into the comprehensive evaluation of AD 0.5 ml syringes, crucial components in medical procedures. These syringes fall into the category of class IIa according to EUMDR and are classified as class II by USFDA. The focus is on assessing their compl...
Open access
Research Article10.9734/jamps/2024/v26i8705
Ensuring the safety and compliance of syringes is crucial in the medical device industry to mitigate risks and uphold quality standards. This research paper examines effective risk management strategies for syringe manufacturers, grounded in the principles outlined in ISO 14971....
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Research Article10.9734/jamps/2024/v26i7702
This paper explores the pivotal role of syringes in the era of precision medicine, shedding light on their historical significance, technological advancements, and the profound impact they have on healthcare quality. By delving into the design features of precision syringes and t...
Open access
Research Article10.9734/jpri/2023/v35i327471
In the healthcare industry, maintaining high-quality standards is crucial to ensure the safety and efficacy of medical products. Good Manufacturing Practices (GMP) provide a set of guidelines and regulations that help ensure the consistent production, control, and quality assuran...
Open access
Research Article10.9734/jpri/2023/v35i187394
Healthcare regulation plays a crucial role in ensuring the quality and accessibility of healthcare services in Canada. This article provides an overview of the healthcare regulatory landscape in Canada, focusing on federal and provincial/territorial regulations. The federal level...
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Research Article10.9734/jpri/2023/v35i187391
This research paper aims to provide a comprehensive analysis of regulatory compliance in the United States, with a specific focus on the guidelines set forth by the United States Food and Drug Administration (USFDA). Regulatory compliance plays a crucial role in ensuring the safe...
Open access
Research Article10.9734/jpri/2023/v35i177389
Regulatory compliance plays a pivotal role in the healthcare industry by ensuring patient safety, maintaining quality standards, and fostering trust between healthcare providers and patients. This research article aims to highlight the significance of regulatory compliance in hea...
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Research Article10.9734/jpri/2023/v35i187390
The European Union Medical Device Regulation (EUMDR 2017/745) requires medical device manufacturers to implement a risk-based approach to quality management system (ISO13485) processes. This article provides an overview of the importance of QMS processes in the medical device ind...
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Research Article10.9734/jpri/2023/v35i137365
Microbiological testing is a critical aspect of the development and evaluation of medical devices, as it plays a vital role in ensuring their safety and efficacy. This article highlights the importance of microbiological testing in medical device development and the various types...
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Research Article10.9734/jpri/2023/v35i127364
Sterilization is a critical aspect of the medical device industry, as the use of improperly sterilized devices can have serious consequences for patients. This article provides an overview of the risks of inadequate sterilization, the methods of sterilization commonly used in the...
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Research Article10.9734/jpri/2023/v35i117358
Surface treatment is a crucial process in the medical device industry that plays a vital role in improving the performance, durability, and safety of medical devices. This article provides an overview of the importance of surface treatment in the medical device industry. The arti...
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Research Article10.9734/jpri/2023/v35i117357
This review paper aims to highlight the crucial role of ISO 10993 standards in ensuring the biocompatibility of medical devices. The use of medical devices has increased rapidly over the years, and it is essential to ensure that these devices do not cause adverse reactions or har...
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Research Article10.9734/jpri/2023/v35i87342
The medical device industry is highly regulated, with a focus on ensuring the safety and effectiveness of medical devices. Risk management is a critical aspect of the medical device industry, involving the identification, assessment, and control of potential risks associated with...
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Research Article10.9734/jpri/2023/v35i67330
The medical device industry is a critical sector that plays a vital role in healthcare delivery. Due to the nature of the work, medical device facilities are at risk of contamination from harmful microorganisms. Fogging is an essential method of disinfection that is used to eradi...
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Research Article10.9734/jpri/2023/v35i47319
Regulatory Affairs experts are the important part of the Medical Device industry since it is concern about the orthopaedic Implant/Instruments lifecycle, it gives key, strategic and functional bearing and backing for working inside guidelines to speed up the turn of events and co...
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Research Article10.9734/cjast/2022/v41i2931797
Medical devices designed for human use can be used to help patients overcome illness or disease and improve their quality of life. Researchers are working with more difficult tasks involved in making a medical device fit for human use. This means that the device should be safe, a...
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Research Article10.9734/jpri/2021/v33i60B34958
In medical device industry the risk management plays a very vital role. There should be proper communication from each and every stakeholder related to risk management of each respective department, it can be Production, Design and Development or Quality Control and all other de...
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Research Article10.9734/jpri/2021/v33i31A31662
Aim: Soybean is well-thought-out to be a major crop owing to its significant involvement as vegetable oil and protein in human diet. However, inopportunely, its production has been melodramatically declined attributable to the commonness of drought related stress. Study Design: D...
Open access
Research Article10.9734/cjast/2021/v40i2531515
Introduction: As an important source of nutrients to humans and animals, soybean is considered to be a major crop. Objective: The present study has been executed to identify diverse soybean genotypes on account of different morpho-physiological and microsatellite molecular marker...
Open access
Research Article10.9734/cjast/2021/v40i2131467