Commission Implementing Regulation (EU) 2019/27 of 19 December 2018 amending Regulation (EU) No 1178/2011 laying down technical requirements and administrative procedures related to civil aviation aircrew pursuant to Regulation (EU) 2018/1139 of the European Parliament and of the Council (Text with EEA relevance.)

Type Implementing Regulation
Publication 2019-01-10
State In force
Text As published
Department European Commission, MOVE
Source EUR-Lex
articles 2

This is the act as published. Later amendments are not folded into the text below: each one is a separate act in this repository and an entry in this law's history.

Reform history JSON API
  • (a) revalidated, provided that the holder:
  • (1) continues to fulfil the general conditions required for medical practice and maintains his or her licence for the practice of medicine;
  • (2) has undertaken refresher training in aviation medicine within the last 3 years;
  • (3) has performed at least 10 aero-medical examinations or equivalent every year;
  • (4) remains in compliance with the terms of the certificate;
  • (5) exercises the privileges in accordance with the requirements of this Annex (Part-MED);
  • (6) has demonstrated that he or she maintains his or her aero-medical competency in accordance with the procedure established by the competent authority.
  • (b) renewed, provided that the holder complies with either the requirements for revalidation set out in point (a) or with all of the following requirements:
  • (1) continues to fulfil the general conditions required for medical practice and maintains his or her licence for the practice of medicine;
  • (2) has undertaken refresher training in aviation medicine within the previous year;
  • (3) has successfully completed practical training within the previous year, either at an AeMC or under the supervision of the competent authority;
  • (4) remains in compliance with the requirements of point MED.D.010;
  • (5) has demonstrated that he or she maintains his or her aero-medical competency in accordance with the procedure established by the competent authority.

SECTION 2

General Medical Practitioners

MED.D.035   Requirements for general medical practitioners

General medical practitioners (GMPs) may act as AMEs for issuing LAPL medical certificates, where they meet all of the following conditions:

  • (a) they exercise their activity in a Member State where GMPs have access to the full medical records of applicants;
  • (b) they exercise their activity in accordance with any additional requirements established in the national law of the Member State of their competent authority;
  • (c) they are fully qualified and licensed for the practice of medicine in accordance with national law of the Member State of their competent authority;
  • (d) they have notified the competent authority before starting such activity.

SECTION 3

Occupational Health Medical Practitioners

MED.D.040   Requirements for occupational health medical practitioners

In Member States where the competent authority is satisfied that the requirements of the national health system applicable to occupational health medical practitioners (OHMPs) are such as to ensure compliance with the requirements of this Annex (Part-MED) applicable to OHMPs, OHMPs may conduct aero-medical assessments of cabin crew, provided that:

  • (a) they are fully qualified and licensed in the practice of medicine and qualified in occupational medicine;
  • (b) the in-flight working environment and safety duties of the cabin crew were included in their occupational medicine qualification syllabus or other training or operational experience;
  • (c) they have notified the competent authority before starting such activity.’.

ANNEX II

The following point is added in Section I of Subpart MED of Annex VI to Regulation (EU) No 1178/2011:

‘ARA.MED.160   Exchange of information on medical certificates through a central repository.

In addition, the Agency and national competent authorities may grant access to EAMR and the information contained therein to other persons, where necessary for the purposes of ensuring the proper functioning of EAMR, in particular its technical maintenance. In that case, the Agency or the national competent authority concerned shall ensure that those persons are duly authorised and qualified, that their access remains limited to what is necessary for the purposes for which they have been granted access and that they have received prior training on the applicable personal data protection legislation and related safeguards. Whenever a competent authority grants a person such access, it shall inform the Agency beforehand.

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Regulation (EC) No 45/2001 of the European Parliament and of the Council of 18 December 2000 on the protection of individuals with regard to the processing of personal data by the Community institutions and bodies and on the free movement of such data (OJ L 8, 12.1.2001, p. 1).

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