Staff Regulations Article 16, Vincenzo Salvatore

La demande est réussie.

Dear European Medicines Agency,

Under the right of access to documents in the EU treaties, as
developed in Regulation 1049/2001, I am requesting all
documentation relating to EMA decisions made, under Article
16 of the Staff Regulations, concerning Vincenzo Salvatore who worked
for EMA. Specifically, I would like to receive a note of all Mr Salvatore's job titles at EMA including dates held, copies of any application(s) that Mr Salvatore made under Article 16 of the Staff Regulations to undertake a new professional activity (including with Sidley Austin LLP), and all correspondence or emails related to the
authorisation of the role or roles.

Yours faithfully,

Vicky Cann

EMA Info, Agence européenne des médicaments

Dear Ms Cann,

Thank you for your e-mail dated on 26 June 2012 in which you apply for access to documents held by the European Medicines Agency.

Provision of information in an open and transparent manner is part of the mission of the Agency.

We will deal with your request as soon as possible and in accordance with the principles and limits established in Regulation (EC) 1049/2001 regarding public access to European Parliament, Council and Commission documents as applicable to the EMA pursuant to article 73 of Regulation (EC) 726/2004.

This regulation sets out provisions which guarantee openness and transparency of the activities of European Institutions, whilst also ensuring the protection of certain public and private interests.

We have reviewed your request and as it concerns a large number of documents, and the Agency has to examine each document individually to ensure that no private or public interests are being compromised, we are not in a position to fulfil your request immediately.

This decision is in line with the principle set out in our policy which states the Agency will apply the principle of proportionality in order to avoid the core business tasks of the Agency and its performance being jeopardised by the administrative workload related to activities within Regulation 1049/2001.

Under the above stated Regulation, you will receive a reply within 30 working days (15 + 15 days extension).

Kind regards,

Document and Information Services

European Medicines Agency
7 Westferry Circus
Canary Wharf
E14 4HB
United Kingdom

[EMA request email]

Frequently Asked Questions (FAQs) have now been published on the Agency's website. It comprises answers to the most commonly asked questions submitted to the EMA. You are invited to consult it at the following Link
This message and any attachment contain information which may be confidential or otherwise protected from disclosure. It is intended for the addressee(s) only and should not be relied upon as legal advice unless it is otherwise stated. If you are not the intended recipient(s) (or authorised by an addressee who received this message), access to this e-mail, or any disclosure or copying of its contents, or any action taken (or not taken) in reliance on it is unauthorised and may be unlawful. If you have received this e-mail in error, please inform the sender immediately.

Afficher les sections citées

Vicky Cann a laissé une remarque ()

Documents have now been received by mail to answer this request. Unfortunately, EMA did not reply elctronically via Ask the EU.