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| home > white papers > 7 Common Myths about QP Training Debunked: A Guide for Senior Managers - RSSL |
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 WHITE PAPERS |
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RSSL
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+44 (0)118 918 4024
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http://www.rssl.com
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University of Reading, Whiteknights Rd, Reading, West Berkshire RG6 6LA
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7 Common Myths about QP Training Debunked: A Guide for Senior Managers
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The role of the Qualified Person (QP) in the pharmaceutical industry is mandated by law (Directive 2001/83/EC, Directive 2001/20/EC, UK SI 2012/1916, UK SI 2004/103). Every holder of a relevant Manufacturers Authorisation (human and veterinary) must have at least one QP; without one, no batch of medicinal product can be certified for release for sale.
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News and Press Releases |
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Evonetix Commences Early Access Program for DNA Synthesised by Thermal Control on its Semiconductor Chip
Cambridge, UK 16th August 2022 – EVONETIX LTD (‘Evonetix’), the
synthetic biology company bringing semiconductor technology to DNA
synthesis, today announced the opening of its early access program for
semiconductor synthesised DNA. Evonetix’s DNA synthesis capability
brings together patented semiconductor chip design and proprietary,
thermally controlled synthesis chemistry, which will be integral to the
Company’s future gene synthesis platforms.
More info >> |
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White Papers |
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Investigator Portals: Facilitating and Streamlining Communication & Collaboration with Study Sites
ArisGlobal
ArisGlobal LLC
Investigator site personnel are often frustrated with the lack of transparency and communication with their sponsors, leading to significant dissatisfaction and withdrawal from current and future studies. The adoption of investigator portals gives sponsors a platform that fosters collaboration and improves site management. Learn about five key areas of sponsor-investigator site interactions deserving of electronic communication and collaboration. Technology and design aspects are also covered.
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