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PHARMACEUTICAL INDUSTRY EVENTS CALENDAR

Temperature Controlled Logistics in Biopharmaceuticals USA 2018

24-25 April 2018
Princeton, USA

After an extremely successful first edition, Temperature Controlled Logistics in Biopharmaceuticals is back in Princeton in April 2018!

Our presenter will proved you with highly informative content about shipping products which must be kept at given temperatures, clinical and commercial operations overviews and real life case studies.

You will enjoy meeting industry leaders to gain insights into new trends for the biopharmaceutical industry and hear opinions and strategies for incorporation into existing processes at your organization. You will have the chance to potentially find solutions to your packaging technology, too!

All of the aspects of the supply chain will be covered, not only cold chain – this way we will have an incredibly holistic view on each step of your work!

The conference is going to be so interactive – you will have the chance to ask questions to senior executives working in so many different departments - Quality, Compliance, Logistics and Packaging.

We’ll see you in Princeton!

 
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Industry Events

Clinical Operations in Oncology Trials West Coast

17-18 November 2020, Hilton San Francisco Airport Bayfront

Clinical Operations in Oncology Trials West Coast will be returning this April for another 2 day event full of thought-provoking presentations, discussions and roundtables. This years' conference highlights include the high-level, interactive immuno-oncology discussion panel where specialists from Shasta Bio Ventures, Abbvie and BeiGene shared their top tips on how to run successful and impactful immuno-oncology studies.
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White Papers

Planning the Execution of a Viral Clearance Study

Eurofins BioPharma Product Testing

Viral clearance studies are a necessary component of any regulatory submission for clinical trials or commercial product approval for all biopharmaceutical products. These studies are performed to evaluate the capability of the purification process to remove or inactivate viruses that could potentially contaminate the starting material. They are complex studies that require substantial financial and personnel resources, as well as specialized scientific expertise to perform. As such, viral clearance studies are often performed at a qualified contract testing laboratory rather than in-house. When multiple parties are involved in this process, clear communication and a comprehensive understanding of the approach and timeline is critical.
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News and Press Releases

Stability Testing and Forced Degradation Stress Tests - Proactive Risk Management

Whereas the durability of many consumables, have a strong tendency to decrease, stability is and remains a crucial factor for pharmaceuticals. That is why the identification and elimination of factors, which put long-term stability at risk, is central during development – and an important requirement concerning the product’s quality.
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