GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • SAGE Publications  (7)
  • 1
    Online Resource
    Online Resource
    SAGE Publications ; 2012
    In:  Journal of Medical Marketing: Device, Diagnostic and Pharmaceutical Marketing Vol. 12, No. 3 ( 2012-08), p. 150-158
    In: Journal of Medical Marketing: Device, Diagnostic and Pharmaceutical Marketing, SAGE Publications, Vol. 12, No. 3 ( 2012-08), p. 150-158
    Type of Medium: Online Resource
    ISSN: 1745-7904 , 1745-7912
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2012
    detail.hit.zdb_id: 2202766-X
    SSG: 3,2
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Online Resource
    Online Resource
    SAGE Publications ; 2020
    In:  Journal of Generic Medicines: The Business Journal for the Generic Medicines Sector Vol. 16, No. 3 ( 2020-09), p. 101-111
    In: Journal of Generic Medicines: The Business Journal for the Generic Medicines Sector, SAGE Publications, Vol. 16, No. 3 ( 2020-09), p. 101-111
    Abstract: Combination products (CPs) are nothing but medical products that do not adequately apt solely into a regulatory category, but reasonably comprise of any combination of drug, device and biological product. The use of combination products and delivery systems are to deal with a chronic condition or to relieve an acute condition or to treat the various lives threaten & complex diseases. This article assesses the regulation of combination products in USA, India, China, Japan and Europe and likens the regulatory regime in pharmaceutical environments. Though many of these types of products have been available for years, recent FDA guidelines have spelled out viewpoint on both a development and commercialization perspective. These elucidations have led to augment regulatory expectations resulting in new and increased challenges. To make sure compliance with these regulations and beat challenges, it is essential to remain familiar with the dynamic changing regulations. This piece of writing spotlights on key aspects to understand the concept of combination products, its classification, review period and most importantly facts to consider when any organization is gearing up for a regulatory submission to regulatory agency and its prospective for PLCM of the combination product.
    Type of Medium: Online Resource
    ISSN: 1741-1343 , 1741-7090
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2020
    detail.hit.zdb_id: 2174701-5
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Online Resource
    Online Resource
    SAGE Publications ; 2021
    In:  Journal of Generic Medicines: The Business Journal for the Generic Medicines Sector Vol. 17, No. 4 ( 2021-12), p. 183-194
    In: Journal of Generic Medicines: The Business Journal for the Generic Medicines Sector, SAGE Publications, Vol. 17, No. 4 ( 2021-12), p. 183-194
    Abstract: 505(b) (2) application is one of the advantageous ways of regulatory submission. This submission approach can lead to fast-track approval for wide-ranging products, exclusively for those that exemplify a limited change from formerly approved drug. Safety and efficacy evidence in terms of non-clinical and clinical portion of the Reference Listed Drug (RLD), are trusted upon. Additionally, supplementary data essentially required to establish comparability with the RLD, are presented in the dossier. Methods This retrospective analysis is to understand the FDA's expectations and avoid errors in terms of data support approval for a new product submitted under the 505 (b) (2) route. The current script is an analysis on how to architect 505(b) (2) regulatory strategy by developing a different set of documents/information. Results The ultimate goal of this review is to allow drug developers to easily navigate through various 505 (b) (2) submissions and defense strategies for registration processes available to the new drug manufacturers and to understand an effective, safer filing route by facilitating early market launch with a prospect of lower cost. Conclusion Before considering option 505 (b) (2), general companies should have a good understanding of product’s potential productivity, scalability, patent infringement, expensive clinical studies and/or non-clinical studies to appropriately strategize scientific and commercial opportunities. This leverage will potentially quicken the development program and will definitely lower the clinical and regulatory risk of new product entrants.
    Type of Medium: Online Resource
    ISSN: 1741-1343 , 1741-7090
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2021
    detail.hit.zdb_id: 2174701-5
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    Online Resource
    Online Resource
    SAGE Publications ; 2013
    In:  Journal of Generic Medicines: The Business Journal for the Generic Medicines Sector Vol. 10, No. 3-4 ( 2013-09), p. 159-171
    In: Journal of Generic Medicines: The Business Journal for the Generic Medicines Sector, SAGE Publications, Vol. 10, No. 3-4 ( 2013-09), p. 159-171
    Abstract: Today medical device sector is evolving to find the new horizons. Medical device approval is a time-consuming process that requires submission of safety, efficacy and quality documentation to national regulatory bodies in various countries. While there are some similarities among the countries regarding medical device regulations, some differences also exist that significantly affect the regulatory scrutiny. This presents a great problem for manufacturers marketing their products in multiple countries. Competent authorities worldwide have begun to realize the problem and collaborate to harmonize the regulations. In the present article regulatory approval procedure is discussed in different jurisdictions such as United States, European Union, Japan, China and India along with comparisons in terms of classification of devices, competent authorities, rules and regulations and quality management systems involved in these countries.
    Type of Medium: Online Resource
    ISSN: 1741-1343 , 1741-7090
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2013
    detail.hit.zdb_id: 2174701-5
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    Online Resource
    Online Resource
    SAGE Publications ; 2021
    In:  Journal of Generic Medicines: The Business Journal for the Generic Medicines Sector Vol. 17, No. 3 ( 2021-09), p. 106-114
    In: Journal of Generic Medicines: The Business Journal for the Generic Medicines Sector, SAGE Publications, Vol. 17, No. 3 ( 2021-09), p. 106-114
    Abstract: China’s pharmaceutical market is growing at a healthy pace. This is due to potential rising per capita income, an increasing elderly population, urbanisation demographics and more access to health care. Methodology The methodology used is a comparative study on the basis of original empirical research. More specifically, the part of examination facts and regulation has been written by conducting empirical research on current international and national resource concerning the subject from books, various guidelines, rules and regulation, articles, published reports and internet. Results Generally the regulatory environment in China has been considered as an very challenging one. From regulatory perspective, CFDA regulations have not been stringent enough nor has it been robust enough to create a quality supply of medications, with (1) concerns in the subject matter, quality comparison between international regulatory standard and usually accepted local products and manufactures set standards; (2) a timeline for regulatory assessment and authorization of new drugs which is much longer in comparison to most countries; (3) less number of regulatory reviewer which has led to a backlog of earlier application. The journey to reshape China from ‘made-in-China’ to ‘discovered-in-China’ is highly challenging. (4) Complications with local protection, corruption and a lack of transparency. The directives from Government has recognized the need for significant system-level transformations for streamlining the pharmaceutical regulatory environment. Conclusion Continuing on the route of reform is promising that all Chinese citizens is eventually having access to safe, effective and high-quality medications in affordable price. These reformations are encouraging and promising not only for China’s health care system, but also for global Pharmaceutical industry and that’s the reason, now many big Pharma companies are considering China as a prime focus. The companies need to make use of the new opportunities, accessible to experience the benefit of faster time-to-market, and cause rewarding growth prospect for both domestic/ multinational companies.
    Type of Medium: Online Resource
    ISSN: 1741-1343 , 1741-7090
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2021
    detail.hit.zdb_id: 2174701-5
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    Online Resource
    Online Resource
    SAGE Publications ; 2013
    In:  Journal of Medical Marketing: Device, Diagnostic and Pharmaceutical Marketing Vol. 13, No. 3 ( 2013-08), p. 171-180
    In: Journal of Medical Marketing: Device, Diagnostic and Pharmaceutical Marketing, SAGE Publications, Vol. 13, No. 3 ( 2013-08), p. 171-180
    Type of Medium: Online Resource
    ISSN: 1745-7904 , 1745-7912
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2013
    detail.hit.zdb_id: 2202766-X
    SSG: 3,2
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 7
    Online Resource
    Online Resource
    SAGE Publications ; 2014
    In:  Journal of Medical Marketing: Device, Diagnostic and Pharmaceutical Marketing Vol. 14, No. 2-3 ( 2014-05), p. 108-114
    In: Journal of Medical Marketing: Device, Diagnostic and Pharmaceutical Marketing, SAGE Publications, Vol. 14, No. 2-3 ( 2014-05), p. 108-114
    Type of Medium: Online Resource
    ISSN: 1745-7904 , 1745-7912
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2014
    detail.hit.zdb_id: 2202766-X
    SSG: 3,2
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...