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Making labels comply with MDR

The new European Medical Devices Regulation (MDR) is forcing companies to review their labeling infrastructure as they battle for organisational preparedness

19th June 2018

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Late to regenerate

Are current regulatory frameworks hindering therapy development for regenerative medicine?

12th June 2018

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Guilty? Are We?

Graham Kershaw, Managing Director of packaging designers and manufacturers, Macpac, addresses consumer and some media concerns in regard to packaging waste – Guilty? Are We?

4th June 2018

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Feeling the pinch

EMIG chairman Leslie Galloway writes about how the fees associated with new regulations on medicines verification are hitting small companies

1st June 2018

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Using real world data in drug discovery

Chris Molloy and James Peach from the Medicine Discovery Catapult talk about humanising discovery and real world evidence and improving access for SMEs to the NHS Ecosystem

24th May 2018

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GDPR: A roadmap to compliance

The steps pharma organisations can take towards GDPR readiness and why the new regulation could be a positive catalyst for change

23rd May 2018

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