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Pharmaceutical Manufacturing and Packing Sourcer
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Created for forward-thinking professionals and businesses, FlyPharma Asia (5-6 March) is the first of FlyPharma’s new and exciting series of conferences for 2018. The event will bring together a global audience of (bio)pharma and logistics professionals to discuss and debate the latest supply chain challenges and industry best practices.
FlyPharma Asia will cover a great wealth of current topics and issues within the regional and global supply chain, as expert speakers impart their knowledge and advice to the audience. With presentations, interactive workshops, and panels, the conference promises to create a dynamic and lively dialogue between all delegates.
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and Technical Advisor Rafik H Bishara, PhD has become one of the most respected figures in the pharmaceutical supply chain distribution sector, following a distinguished 35-year career with Eli Lilly & Co as Director, Quality Knowledge Management, and Technical Support.
Throughout his career, Dr Bishara has worked consistently towards harmonisation of many global regulations and guidelines for the handling, storage, and transportation of pharmaceutical and biotech products. He has chaired and presented at industry-leading conferences, has authored numerous articles, and has technically advised several organisations on good cold chain and temperaturecontrolled management. His current focus is on secure temperaturecontrolled supply chains.
Drawing upon his extensive background from within the pharma and logistics industries, in his role as FlyPharma Chair and Technical Advisor, he will guide delegates through each day’s agenda and prompt the audience to question key points from each session, creating a dynamic and engaging discussion.
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News and Press Releases |
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PHARM Connect 2019
Life science and business are going to meet at PHARM Connect on the
12-13 of March 2019 in Budapest, Hungary to continue the tradition of
providing high calibre, customised professional partnering opportunities
for pharma and biotech professionals from Central & Eastern
European and beyond and deliver the crucial information they need to
excel in their work. The influential annual gathering brings together
over 400 global and regional decision-makers, top scientists, industry
executives and business development leaders for the ninth time to
identify new business opportunities, technologies, state-of-the-art
formulation development strategies and to foster exchange of ideas on
the role of the sector.
More info >> |
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White Papers |
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Recommendations for Implementing Assessment Criteria Guidelines in Lymphoma and Chronic Lymphocytic Leukemia Clinical Trials
Perceptive Informatics
Standardized assessment criteria are becoming increasingly important in obtaining valid outcomes in oncology clinical trials. While standardized criteria encourage a more uniform approach to assessing clinical trial data, they are often subject to the interpretation of the user. These differences in interpretation, while seemingly minor, can have a major impact on assessments. The most commonly used standardized criteria for lymphoma have been no exception. Differences such as minimum new lesion size, lymph node normalization size requirements, inclusion of extranodal lesions and assessment of organomegaly can have a profound effect on overall response. Additionally, heightened scrutiny of the assessment criteria used in a given protocol can lead to questions about a drug’s efficacy if not applied correctly according to regulators’ interpretation.
More info >> |
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Industry Events |
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Pharma Packaging and Labelling East Coast 2019
20-21 February 2019, Phildaelphia, USA
Now
in its 11th year, Pharma Packaging and Labeling is back to deliver key,
actionable insights into very latest regulatory requirements, technological
innovations, strategic developments, and how to implement them into your
packaging and labeling chain with both maximum efficiency and minimal cost.
More info >> |
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