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Pharmaceutical Manufacturing and Packing Sourcer
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Adopting real-time environmental conditions monitoring in the clinical trial supply chain is becoming increasingly straightforward, with technological development offering smaller, more affordable solutions with better connection options. However, merely discussing features or pricing does not in itself help with answering why this kind of technology would be important to fulfil specific operational needs. Looking beyond technology features and considering instead the drivers and benefits of digitalising monitoring activities in the logistics chain is imperative.
Let’s begin by looking at some of the drivers behind why real-time monitoring should be implemented to logistics operations, so a shared understanding on why the matter is being discussed in the first place can be gained. These drivers can be divided roughly into three categories of operational efficiency, regulatory demands, and technological developments, which all affect each other in myriad ways.
Need to Exceed
Arguably, beginning with operational efficiency is easiest because organisations have the most intimate experience with this. Multiple stakeholders, even within a single company, are constantly looking to develop improved processes for quality management, more efficient operations, cost savings, or other such purposes.
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News and Press Releases |
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Drive for generics sees Korea increasingly attractive to international pharma
Amsterdam, 31st July 2019: Already home to more than 40 pharmaceutical
multinationals, Korea is on course to become a global biotech and
pharmaceutical hub by 2025, driven by the surge of international
partnerships, biosimilars, an expansion in the export of finished
formulations and a robust generics market.
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White Papers |
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PhlexEarchive: The Right Solution for Electronic Archiving of TMF Content
Phlexglobal Ltd
Many sponsor organizations have already recognized the value of moving from paper to electronic Trial Master Files (eTMFs). But few sponsors have taken a more holistic approach to the TMF lifecycle and looked at the entire process from study start-up through archiving of the TMF in electronic format, also known as e-archiving. The recurring value of managing, tracking, maintaining and accessing electronic files should not stop at the point of archiving. All of the challenges of managing an active paper TMF carry through to a paper archive. All of the benefits of an electronic TMF also carry through to the electronic archive.
As companies look to move their compliance assets to secure, long-term storage, it is important to consider ongoing compliance requirements, security, accessibility, efficiency and costs of archiving TMF content in a digital format.
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Industry Events |
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CPhI & P-MEC India
26-28 November 2019, India Expo Centre, Greater Noida, Delhi NCR, India
As the pharma industry looks increasingly towards India for high quality,
low cost pharma solutions, CPhI & P-MEC India is the ideal event for companies
wanting to pick up on the latest trends and innovations the market has to
offer. At CPhI & P-MEC India, you will meet the movers and shakers from
India's pharma machinery, technology and ingredients industries, giving you a
competitive advantage that will help grow your business.
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