EUR-Lex & EU Commission AI-Powered Semantic Search Engine
Modern Legal
  • Query in any language with multilingual search
  • Access EUR-Lex and EU Commission case law
  • See relevant paragraphs highlighted instantly
Start free trial

Similar Documents

Explore similar documents to your case.

We Found Similar Cases for You

Sign up for free to view them and see the most relevant paragraphs highlighted.

Case T-511/14: Order of the General Court of 25 October 2017 — Novartis Europharm v Commission (Medicinal products for human use — Marketing authorisation for the medicinal product Zoledronic acid Teva Generics — Zoledronic acid — Period of protection of the medicinal product Aclasta containing the active substance zoledronic acid — Withdrawal of the contested measure — No need to adjudicate)

ECLI:EU:UNKNOWN:62014TB0511

62014TB0511

October 25, 2017
With Google you find a lot.
With us you find everything. Try it now!

I imagine what I want to write in my case, I write it in the search engine and I get exactly what I wanted. Thank you!

Valentina R., lawyer

8.1.2018

Official Journal of the European Union

C 5/42

(Case T-511/14) (<span class="super note-tag">1</span>)

((Medicinal products for human use - Marketing authorisation for the medicinal product Zoledronic acid Teva Generics - Zoledronic acid - Period of protection of the medicinal product Aclasta containing the active substance zoledronic acid - Withdrawal of the contested measure - No need to adjudicate))

(2018/C 005/56)

Language of the case: English

Parties

Applicant: Novartis Europharm Ltd (Camberley, United Kingdom) (represented by: C. Schoonderbeek, lawyer)

Defendant: European Commission (represented by: A. Sipos and M. Wilderspin, Agents)

Re:

Action brought under Article 263 TFEU seeking annulment of Commission Implementing Decision C(2014) 2155 final of 27 March 2014 granting a marketing authorisation to Teva Generics BV for the medicinal product for human use Zoledronic acid Teva Generics — Zoledronic Acid under Article 3 of Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Community procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (OJ 2004 L 136, p. 1).

Operative part of the order

1.There is no longer any need to adjudicate on the action.

2.There is no longer any need to adjudicate on Teva BV’s application for leave to intervene.

3.Each party shall bear its own costs.

(<span class="super">1</span>) OJ C 388, 3.11.2014.

EurLex Case Law

AI-Powered Case Law Search

Query in any language with multilingual search
Access EUR-Lex and EU Commission case law
See relevant paragraphs highlighted instantly

Get Instant Answers to Your Legal Questions

Cancel your subscription anytime, no questions asked.Start 14-Day Free Trial

At Modern Legal, we’re building the world’s best search engine for legal professionals. Access EU and global case law with AI-powered precision, saving you time and delivering relevant insights instantly.

Contact Us

Tivolska cesta 48, 1000 Ljubljana, Slovenia