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Sie suchen in allen Bereichen und nach dem Autor Röhrig B.

In der Rubrik Zeitschriften haben wir 6 Beiträge für Sie gefunden

  1. Merken

    EMA and EU Commission – Topical News

    Rubrik: europharm®

    (Treffer aus pharmind, Nr. 03, Seite 373 (2015))

    Röhrig B

    EMA and EU Commission – Topical News / Functional specifications for the EU portal and EU database to be audited (EMA/42176/2014) and Draft proposal for an addendum, on transparency, to the “Functional specifications for the EU portal and EU database to be audited” (EMA/641479/2014) – Part II*Part I s. Pharm Ind. 2015;77(2):213–215 · Röhrig B · Rechtsanwaltskanzlei Dr. Brigitte Röhrig, Betzdorf/Sieg (Germany)
    Regulation No. 536/2014/EU (hereinafter Clinical Trial Regulation = CTR) lays down the future provisions governing the conduct of clinical trials in the EU. The application of the new system requires the functioning of the EU portal and EU database. To this end, Commission and EMA are already preparing the executive documents for functioning of the EU database and EU portal as well as the characteristics to be audited by the EMA management board. The EMA published two documents, one document on “Functional specifications for the EU portal and EU database to be audited (EMA/42176/2014)” and a “draft proposal for an addendum, ...

  2. Merken

    EMA and EU Commission – Topical News

    Rubrik: europharm®

    (Treffer aus pharmind, Nr. 02, Seite 213 (2015))

    Röhrig B

    EMA and EU Commission – Topical News / Functional specifications for the EU portal and EU database to be audited (EMA/42176/2014) and Draft proposal for an addendum, on transparency, to the “Functional specifications for the EU portal and EU database to be audited” (EMA/641479/2014) – Part I · Röhrig B · Rechtsanwaltskanzlei Dr. Brigitte Röhrig, Betzdorf/Sieg (Germany)
    Regulation No. 536/2014/EU (hereinafter Clinical Trial Regulation=CTR) lays down the future provisions governing the conduct of clinical trials in the EU. It follows a harmonised approach relating to submission, assessment and reporting of clinical trials as well as the adverse reactions happening during the conduct of a clinical trial. Crucial elements of this harmonised approach are the EU portal with the EU database, through which all communications shall take place. The EU portal for clinical trials shall serve as single entry point for the submission of data and all information relating to clinical trials. The information which is entered through ...

  3. Merken

    EMA and EU Commission – Topical News

    Rubrik: europharm®

    (Treffer aus pharmind, Nr. 11, Seite 1732 (2014))

    Röhrig B

    EMA and EU Commission – Topical News / New Regulation No. 536/2014/EU on Clinical Trials for Medicinal Products for Human Use and Repeal of Directive 2001/20/EC adopted on 16 April 2014 (Part 4*Part 1 s. Pharm. Ind. 2014;76(7):1083–1085, Part 2 s. Pharm. Ind. 2014;76(8):1220–1222 and Part 3 s. Pharm. Ind. 2014;76(9):1420–1423: Modification of Clinical Trials) · Röhrig B · Rechtsanwaltskanzlei Dr. Brigitte Röhrig, Betzdorf/Sieg (Germany)
    Regulation No. 536/2014/EU (hereinafter Clinical Trial Regulation = CTR) lays down the future provisions governing the conduct of clinical trials in EU. Most probably it will start to be applicable as of 28 May 2016, if the EU portal as well as the EU database which have to be set up in this system, have achieved full functionality and the systems meet the functional specifications drawn up in the respective Commission Regulations to be set up; Art. 99, 82 (3) of the Regulation. The new Regulation is immediately applicable in all Member States without needing any provisions to transform the principles ...

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