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Key EU Regulatory Developments in the Pharmaceutical Sector (2019-2020): Implications in Practice

e-Presentation by Elisabethann Wright

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Foto: Key EU Regulatory Developments in the Pharmaceutical Sector (2019-2020): Implications in Practice.

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Year: 2020

Topic

After giving a critical appraisal of the consequences of recent judgments adopted by the CJEU on access to documents held by EMA, this e-presentation presents some of the industry challenges raised by the implementation of the new in-vitro diagnostic regulation, as well as by Brexit.

Speaker

Elisabethann Wright, Partner Practising in the Life Sciences Sector, Hogan Lovells International LLP, Brussels.

Package

  • Video presentation
  • Audio podcast version
  • Duration: 42 minutes
  • Links to all relevant sources of law
  • Access for 12 months after purchase
  • Includes standard version and certified version eligible for CPD points

Technical requirements

The e-presentation should work in any internet browser. If you encounter difficulties, please ensure that you have javascript enabled (go to www.whatismybrowser.com or ask your system administrator).

Filmed at ERA's Annual Conference on EU Law in the Pharmaceutical Sector 2020 in Brussels, 5-6 March 2020.

Access

To obtain immediate access to this e-presentation, please pay by credit card. You can also pay by invoice (bank transfer) but access will only be granted when payment has been received. For multiple registrations, please click here.


Certified Version eligible for CPD points

This version requires you to view the full e-presentation and to take a short quiz at the end. A certificate can then be issued entitling you to CPD points in selected jurisdictions.

If you would like to claim a certificate please send your request to elearning@era.int.
Area of Law: Health & Pharmaceutical Law

Language: English

Article-no.: 220P08

Price: 30,00 EUR


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