Eesti esindaja nimetamine

Tiiu Noobel From: Jakimiuk Marta <[email protected]> Sent: teisipäev, 3. märts 2026 13:25 To: Tiiu Noobel Cc: Jenas Kärolin Subject: RE: Estonia - 2026-02-16 - Nomination invitation letter for CAT alternate Attachments: Estonia - 2026-02-16 - Nomination invitation letter for CAT alternate - Pille Saalik_.pdf Importance: High Follow Up Flag: Follow up Flag Status: Flagged Dear Tiiu Noobel, Further to the below correspondence, a ached please find the nomina on le er for Estonia. Kind regards, Marta Jakimiuk Experts and Declarations of Interests Management Meeting Secretariat Office Committees and Quality Assurance Department European Medicines Agency Domenico Scarlattilaan 6, 1083 HS Amsterdam, The Netherlands Tel. +31 (0)88 781 8354 [email protected] | www.ema.europa.eu | For directions, see How to find us Follow us: 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.  Please consider the environment before printing this e-mail Classified as internal/staff & contractors by the European Medicines Agency From: Jakimiuk Marta Sent: Monday, 2 March 2026 10:16 To: Tiiu Noobel <[email protected]>; Executive.Director <[email protected]>; Nominations <[email protected]> Cc: Jenas Kärolin <[email protected]> Subject: RE: Estonia - 2026-02-16 - Nomination invitation letter for CAT alternate Dear Tiiu Noobel, 1 Apologies for the inconvenience, it was an error when conver ng few files into PDF at the same me. We will forward the correct le er as soon as possible. Kind regards, Marta Jakimiuk Experts and Declarations of Interests Management Meeting Secretariat Office Committees and Quality Assurance Department European Medicines Agency Domenico Scarlattilaan 6, 1083 HS Amsterdam, The Netherlands Tel. +31 (0)88 781 8354 [email protected] | www.ema.europa.eu | For directions, see How to find us Follow us: 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.  Please consider the environment before printing this e-mail From: Tiiu Noobel <[email protected]> Sent: Monday, 2 March 2026 10:00 To: Executive.Director <[email protected]>; Nominations <[email protected]> Cc: Jenas Kärolin <[email protected]>; Jakimiuk Marta <[email protected]> Subject: FW: Estonia - 2026-02-16 - Nomination invitation letter for CAT alternate Some people who received this message don't often get email from [email protected]. Learn why this is important Dear Executive Director, Dear Nomination Team, I have not received an answer to my letter below, so I am sending it agin. Is there a letter also for Estonia? This one is addressed to Latvia. With best regards, Tiiu Noobel From: Tiiu Noobel Sent: Monday, February 23, 2026 3:20 PM To: '[email protected]' <[email protected]> Subject: FW: Estonia - 2026-02-16 - Nomination invitation letter for CAT alternate Dear Marta Jakimiuk, 2 Thank you but the attached letter is about Latvia. Is there letter also for Estonia? With best regards, Tiiu Noobel Secretary Permanent Representation of Estonia to the EU Rue Guimard 11/13, 1040 Brussels Tel: +32 2227 4337, [email protected] https://eu.mfa.ee From: Esindus EL juures üldaadress <[email protected]> Sent: Monday, February 23, 2026 1:00 PM To: Tiiu Noobel <[email protected]> Subject: FW: Estonia - 2026-02-16 - Nomination invitation letter for CAT alternate From: Jakimiuk Marta <[email protected]> Sent: Monday, February 23, 2026 12:31 PM To: Esindus EL juures üldaadress <[email protected]> Cc: Kompus Mairi <[email protected]>; Jenas Kärolin <[email protected]>; Saalik Pille <[email protected]>; Maimets Toivo <[email protected]>; Kiisk Katrin <[email protected]>; Nominations <[email protected]> Subject: Estonia - 2026-02-16 - Nomination invitation letter for CAT alternate Your Excellency, Please find attached a letter signed by the European Medicines Agency's Executive Director requesting the nomination of a representative to the Agency's Scientific Committees. The letter is accompanied by: • Annex B • Committee composition and expertise You are kindly invited to address nominations to the European Medicines Agency’s Executive Director at [email protected] (with copy to [email protected]). Please do not hesitate to contact me should you have any questions regarding this request for nomination. For the information of the National Competent Authority in cc of this email The nominee, if not registered in Experts Management Tool, will be required to register at: https://experts.ema.europa.eu/ • Registering in the Experts Management Tool, experts will be required to provide: Contact details and areas of expertise, Declaration of Interests, Curriculum Vitae. This should be completed with as much detail as possible. • Instructions on how to register in the Experts Management Tool can be found in this user manual (link). The EMA policy and guidance document can be found on the EMA website: • European Medicines Agency policy on the handling of competing interests of scientific committees’ members and experts (link) • Procedural guidance on inclusion of declared interests in the European Medicines Agency’s declaration of interests (for scientific committees’ members and experts) (link) 3 Nominees will be subject to a pre-screening of any declared competing interest in line with the Agency's policy on handling of competing interests. In case of a negative outcome, the Agency will provide feedback of this screening to the nominating authority for subsequent consideration. I would like to emphasize the importance of a timely nomination of a committee member to ensure the continuous representation of your Member State in the Committee. To avoid a vacant committee member position when an alternate position is already filled, you may consider nominating the alternate (temporarily) as member. Please also inform me if you intend to keep the position temporarily vacant. If no nomination is received, the position will be considered temporarily vacant until a nomination is received. Sincerely yours, Marta Jakimiuk Experts and Declarations of Interests Management Meeting Secretariat Office Committees and Quality Assurance Department European Medicines Agency Domenico Scarlattilaan 6, 1083 HS Amsterdam, The Netherlands Tel. +31 (0)88 781 8354 [email protected] | www.ema.europa.eu | For directions, see How to find us Follow us: 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.  Please consider the environment before printing this e-mail Classified as internal/staff & contractors by the European Medicines Agency 4 HE the Ambassador Permanent Representation of Estonia Rue Guimard 11–13 B-1040 Bruxelles BELGIUM 16 February 2026 EMA/38705/2026 Executive Director Your Excellency, Subject: Nomination of representatives in the Committee for Advanced Therapies (CAT) of the European Medicines Agency In accordance with Regulation (EC) No 726/2004, members and alternates of the European Medicines Agency’s Management Board and scientific committees are nominated for a three-year mandate by EU member states and EEA-EFTA countries. The three-year mandate of the representative listed below is due to expire. I, therefore, invite you to nominate representative for a new three-year mandate starting from the date indicated below. In case you are nominating new representative and a different start date for the mandate is envisaged, please inform me accordingly. • Pille Saalik Alternate 01 April 2026 Please also inform me if you intend to keep the position temporarily vacant. If no nomination is received, the position will be considered temporarily vacant until a nomination is received. In making your nominations, please note that the Agency’s Management Board has determined that members of scientific committees should meet conditions concerning their declarations of interests as described in the Policy on the handling of competing interests of scientific committees’ members and experts. This policy can be found on the EMA website. I would like to draw your attention to the attached Annex B, which lists the recommended criteria for experience and expertise of the Committee members and alternates for consideration when nominating a new representative. As agreed with the network of the Heads of Medicines Agencies in order to address the increasing complexity in scientific developments related to the Committee’s activities, the current expertise of the Committee and the expertise required for upcoming procedures are monitored. It would be appreciated if the following specific areas of expertise that were identified as desirable for the current and upcoming work of the Committee, could be taken into consideration when nominating a new representative, subject to the availability of such expertise to the relevant competent authority in your country: • Real world evidence (epidemiologist) • Clinical trial methodology – single-arm clinical trials (biostatistician) • Pharmacovigilance (liaison with PRAC) • Medical devices • Clinical experience with advanced therapy medicinal products • Non-clinical experience with advanced therapy medicinal products − NCA staff member preferred as member and academic as alternate. An overview of the current composition of the Committee and the expertise of its members is attached for your information. Please address the nomination to my attention at [email protected] (with copy to [email protected]), indicating full contact details for the nominee and the start date of the mandate, together with any additional information you believe may assist this nomination. In case you already provided me with your nomination, I kindly ask you to disregard this correspondence. Yours faithfully, Digitally signed by Emer Cooke Emer Cooke Date: 2026.03.02 18:41:03 +01'00' Emer Cooke Executive Director Encs: Annex B Current committee composition and expertise EMA/38705/2026 Page 2/2 22 June 2017 EMA/517622/2015 Inspections, Human Medicines Pharmacovigilance and Committees Recommendation on criteria for experience and expertise of CAT members and alternates Legislation Article 21 (1) of Regulation (EC) No 1394/2007 states that the Committee for Advanced Therapies (CAT) shall be composed of the following members: (a) five members or co-opted members of the Committee for Medicinal Products for Human Use from five Member States, with alternates either proposed by their respective Member State or, in the case of co-opted members of the Committee for Medicinal Products for Human Use, identified by the latter on the advice of the corresponding co-opted member. These five members with their alternates shall be appointed by the Committee for Medicinal Products for Human Use; (b) one member and one alternate appointed by each Member State whose national competent authority is not represented among the members and alternates appointed by the Committee for Medicinal Products for Human Use. Article 21 (2) states that all members of the CAT shall be chosen for their scientific qualification or experience in respect of advanced therapy medicinal products. For the purposes of paragraph 1(b), the Member States shall cooperate, under the coordination of the Executive Director of the Agency, in order to ensure that the final composition of the Committee for Advanced Therapies provides appropriate and balanced coverage of the scientific areas relevant to advanced therapies, including medical devices, tissue engineering, gene therapy, cell therapy, biotechnology, surgery, pharmacovigilance, risk management and ethics. At least two members and two alternates of the Committee for Advanced Therapies shall have scientific expertise in medical devices. Recommendation The following recommendation on criteria for experience and expertise is made to nominating authorities in the Member States for consideration when the Agency invites them to nominate a new CAT member and alternate. CHMP members and their alternates are invited to bear this recommendation in mind when considering putting themselves forward for a CHMP-CAT joint membership: 30 Churchill Place ● Canary Wharf ● London E14 5EU ● United Kingdom Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5520 Send a question via our website www.ema.europa.eu/contact An agency of the European Union © European Medicines Agency, 2017. Reproduction is authorised provided the source is acknowledged.  Academic expertise in the relevant scientific area, such as:  Internationally recognised academic qualification(s)/accreditation(s) (e.g. degrees, diplomas, post graduate qualifications (e.g. PhD), professional affiliations etc.) in life sciences or physical sciences (medicine, pharmacy, chemistry, biology, …)  Delivering scientific expert views/opinions to National/European/International scientific bodies.  Direct working experience, after obtaining the academic qualification, in the relevant scientific area, in a national competent authority, industry and/or academia/clinical practice (university, hospital, research facility, private practise, etc.). Relevant experience will depend on the core activities of the Committee but could be expected to include experience in one or more of the following areas:  Clinical expertise in one or more therapeutic areas (either as a medical doctor or as a hospital pharmacist)  Clinical co-ordinator/investigator in clinical trials  Member of Data Safety Monitoring Board or Scientific Advisory Board and/or experience of working in or with ethics approval committees  Pre-clinical research and expertise (e.g. in toxicology, pharmacology, animal models)  Clinical research (e.g. clinical trials, epidemiological studies)  Research in the relevant “quality” areas, relating to the research and development of medicinal products (e.g. molecular biology, gene technology)  Formulation, manufacture and control of medicinal products  Pharmacovigilance and risk management  Advisory experience (leading to knowledge of regulatory requirements) in committees’/ scientific bodies’ activities (e.g. member of Working Party or SAG, nominated by EMA or NCA for involvement in EMA activities, experience in providing scientific advice for central and/or national MAs, involvement in WHO, EDQM, FDA activities)  Experience in the review of dossiers, preparation and provision of assessments reports for central and/or national MAAs, experience in peer review of Assessment Reports/List of Questions  Targeted publications in recognised and peer-reviewed scientific journals and/or peer reviewing activities for scientific journals  Members and alternates nominated to the CAT would be expected to have expertise in one of the areas of expertise relevant to advanced therapy medicinal products required by the legislation and/or in one of the additional areas of expertise identified by the Committee:  Areas of expertise relevant to advanced therapy medicinal products as per legal requirement:  cell therapy  gene therapy  tissue engineering  biotechnology  medical devices Recommendation on criteria for experience and expertise of CAT members and alternates EMA/517622/2015 Page 2/3   surgery  pharmacovigilance  risk management  ethics  Additional areas of expertise identified by the Committee  Pre-clinical experience with advanced therapy medicinal products  Clinical experience with advanced therapy medicinal products  Biostatistics  Clinical trial methodology and clinical trials Whilst a minimum period for such post graduate experience is not defined, please note for information, that the length of experience of CHMP and PRAC members and alternates in June 2015 ranged from 2 to 40 years and in 2 out of 3 cases the member had a greater number of years of relevant experience compared to the alternate. Recommendation on criteria for experience and expertise of CAT members and alternates EMA/517622/2015 Page 3/3