Chapter 1 Licensing |
Section 1 Subject Matter |
Art. 12
A licence as specified in Article 8 paragraph 1 of the Act is required by any person who, as holder of a cantonal professional practising licence, independently or as a team leader:
2 Amended by No I of the O of 21 June 2017, in force since 1 Sept. 2017 (AS 2017 3651). |
Section 2 Licence Requirements |
Art. 2 Evidence of qualifications for the use of assisted reproductive techniques 3
Any person who uses assisted reproductive techniques requires:
1bis It may be assumed that a person has the qualifications specified in paragraph 1 letter b if he or she meets the requirements of Annex 3.5 1ter The Federal Department of Home Affairs may amend Annex 3 if amendments to the professional requirements for the use of assisted reproductive techniques so require.6 2 Any person who limits the activity to insemination with sperm cells from a third party requires: the Swiss obstetrics and gynaecology specialist title or an equivalent recognised foreign specialist title; and the cantonal licence to practise as an independent professional. 3 Amended by No I of the O of 21 June 2017, in force since 1 Sept. 2017 (AS 2017 3651). 4 Amended by Annex 6 No II 2 of the O of 23 Sept. 2022 on Human Genetic Testing, in force since 1 Dec. 2022 (AS 2022 585). 5 Inserted by Annex 6 No II 2 of the O of 23 Sept. 2022 on Human Genetic Testing, in force since 1 Dec. 2022 (AS 2022 585). 6 Inserted by Annex 6 No II 2 of the O of 23 Sept. 2022 on Human Genetic Testing, in force since 1 Dec. 2022 (AS 2022 585). |
Art. 3 Evidence of qualifications to preserve and supply reproductive material 7
Any person who receives reproductive cells, impregnated ova or embryos in vitro for preservation or arranges the supply of donated sperm cells without personally using assisted reproductive techniques requires: a Swiss or a recognised foreign medical specialist title; and the cantonal licence to practise as an independent professional. 7 Amended by No I of the O of 21 June 2017, in force since 1 Sept. 2017 (AS 2017 3651). |
Art. 4 Reproductive medicine laboratory 8
1 Any person who uses reproductive techniques requires a reproductive medicine laboratory that meets the following requirements:
2 The Federal Department of Home Affairs may update Annex 2 in line with international or technical developments. In consultation with the Federal Department of Economic Affairs, Education and Research, it shall make updates that may have the effect of being technical barriers to trade. 8 Amended by No I of the O of 21 June 2017, in force since 1 Sept. 2017 (AS 2017 3651). |
Art. 5 Use of donated sperm cells
1 Any person wishing to use assisted reproductive techniques using donated sperm cells must indicate in the application:
2 Any person wishing to supply donated sperm cells must indicate:
3 Any changes are to be notified to the supervisory authority. |
Art. 6 Counselling and care 11
1 Together with the application for a licence to use assisted reproductive techniques, plans must submitted for the provision of social psychological counselling and support, as specified in Article 9 paragraph 2 letter c of the Act. 2 Where it is planned to use reproductive techniques with an analysis of the genetic material of reproductive cells or embryos in vitro or with the selection of donor sperm cells to prevent the transmission of a serious illness, a proposal with regard to genetic counselling in accordance with Article 6a of the Act must be submitted. 11 Amended by No I of the O of 21 June 2017, in force since 1 Sept. 2017 (AS 2017 3651). |
Section 3 Licensing and Supervision |
Art. 8 Responsibility
1 The body responsible for licensing and supervision shall be the department responsible for healthcare in the canton where the activity specified in Article 8 paragraph 1 of the Act is carried out. 2 The cantons may designate another authority which has the necessary expertise. |
Art. 9 Licensing
1 The licence to use assisted reproductive techniques may be restricted to certain techniques. 2 The licence may be granted for a limited term and subject to conditions. 3 ...12 12 Repealed by No I of the O of 21 June 2017, with effect from 1 Sept. 2017 (AS 2017 3651). |
Art. 10 Supervision 13
1 Within a year of granting a licence, the supervisory authority shall arrange for an inspection to be carried out by an expert. Thereafter, an inspection shall be carried out as often as necessary, but at least once every three years. 2 The supervisory authority may consult an independent expert. 3 Persons charged with carrying out an inspection shall be granted access at all times to the premises and facilities used to perform the activities concerned. 3 If the laboratory is accredited under the Accreditation and Designation Ordinance of 17 June 199614, the supervisory authority may dispense with all or part of the review of the quality management system. 4 The Swiss Accreditation Service shall notify the supervisory authority within an appropriate period of accreditations that have been granted or renewed as well as of any that have been suspended or revoked. 13 Amended by No I of the O of 21 June 2017, in force since 1 Sept. 2017 (AS 2017 3651). |
Art. 11 and 1215
15 Repealed by No I of the O of 21 June 2017, with effect from 1 Sept. 2017 (AS 2017 3651). |
Art. 14 Reporting
1 Licence holders must submit an annual report on their activities, as specified in Article 11 of the Act, to the supervisory authority by no later than 1 May of the following year. 2 The supervisory authority shall transmit the anonymised data to the Federal Statistical Office by no later than 1 July of the year in question for evaluation and publication. The data must not include any indication of the centres of reproductive medicine. 3 The Federal Statistical Office shall provide the supervisory authorities with a form for standardised data collection. This may also be used for the annual report on activities referred to in paragraph 1. |
Art. 14a Evaluation 16
The supervisory authority shall on request send the Federal Office of Public Health the data required for the evaluation in accordance with Article 14a paragraph 2 letter c of the Act together with the contact details for licence holders in accordance with Article 8 paragraph 1 of the Act. 16 Inserted by No I of the O of 21 June 2017, in force since 1 Sept. 2017 (AS 2017 3651). |
Chapter 2 Data on Biological Origins |
Section 1 Donor Data Register 17
17 Amended by No I of the O of 31 Oct. 2012, in force since 1 Jan. 2013 (AS 20126097). |
Art. 15 Competent authority 18
1 The Federal Civil Status Office (Federal Office) shall keep a register for storing the sperm donor data specified in Article 24 of the Act (donor data register). 2 The Federal Office shall issue processing regulations governing the establishment and management of the donor data register, and defining in particular the structure, procedures and access rights. 18 Amended by No I of the O of 31 Oct. 2012, in force since 1 Jan. 2013 (AS 20126097). |
Art. 15a Online management 19
1 The donor data register is kept electronically. 2 The transmitted data are stored in electronic form. 3 The electronic system for the management of the register and for storing the data must meet the following requirements:
19 Inserted by No I of the O of 31 Oct. 2012, in force since 1 Jan. 2013 (AS 20126097). |
Art. 15b Structure of the donor data register 20
1 The register contains a directory of the sperm donors. 2 Each sperm donor file contains the following information:
20 Inserted by No I of the O of 31 Oct. 2012, in force since 1 Jan. 2013 (AS 20126097). |
Art. 16 Transmission of the data to the Federal Office 21
1 The data are transmitted by the attending doctor to the Federal Office in accordance with Articles 24 and 25 of the Act at the same time as the report of the sperm donor data; the form may be transmitted on paper (Art. 16a) or electronically (Art. 16b); the Federal Office issues the form. 2 The other data may be transmitted at a time later than that specified in paragraph 1. 3 The registration form for sperm donor data contains the following data:
21 Amended by No I of the O of 31 Oct. 2012, in force since 1 Jan. 2012 (AS 20126097). 22 Amended by No II of the O of 30 March 2022, in force since 1 July 2022 (AS 2022 243). |
Art. 16a Transmission in paper form 23
1 If the form is completed by hand, it must be completed legibly in block capitals and signed. 2 If the form is illegible, incomplete, not signed or defective in some other way, the Federal Office may return it to the doctor, giving notice that he or she will be in breach of the obligation under Article 25 of the Act to transmit the data if the noted defects are not rectified. 3Data may be transmitted in accordance with Article 24 of the Act and Article 17 of this Ordinance by registered post or by private courier. 23 Inserted by No I of the O of 31 Oct. 2012, in force since 1 Jan. 2012 (AS 20126097). |
Art. 16b Transmission in electronic form 24
1 The Federal Office may request doctors who wish to transmit the data electronically that they register with a recognised platform for the secure service in accordance with Article 2 the Ordinance of 18 June 201025 on Electronic Service in Civil and Criminal Proceedings and Debt Enforcement and Bankruptcy Procedures. 2 The doctors shall use the electronic form provided by the Federal Office on its website, on the secure service platform or by post. 3 The form must bear a qualified electronic signature in accordance with Article 2 of the Federal Act of 18 March 201626 on Electronic Signatures.27 4 A certified electronic signature is not required if identification of the sender and the integrity of the transmission is guaranteed in some other suitable way. 5 The result of the medical examinations is transmitted to the Federal Office in PDF/A format. 6 The doctors shall send documents that are not electronically transmitted by registered post or by private courier to the Federal Office. 7 The electronic files shall be transmitted to the electronic postal address of the Federal Office and encrypted using its public key. 8 Registration with the secure service platform is deemed to be consent to the Federal Office serving documents electronically. Consent may be revoked at any time. 9 The principles relating to the detection and rectification of defects in forms transmitted on paper (Art. 16a para. 2) apply mutatis mutandis. 24 Inserted by No I of the O of 31 Oct. 2012, in force since 1 Jan. 2013 (AS 20126097). 27 Amended by Annex No II 8 of the O of 23 Nov. 2016 on Electronic Signatures, in force since 1 Jan. 2017 (AS 2016 4667). |
Art. 18 Updating of stored data 28
At the request of the treated couple, the data held in the donor data register shall be updated. The couple shall provide the information required for this purpose. 28 Amended by No I of the O of 31 Oct. 2012, in force since 1 Jan. 2013 (AS 20126097). |
Art. 19 Security of stored data 29
1 The Federal Office shall ensure that the data in the donor data register and the data in accordance with Article 15b paragraph 2 are securely stored in accordance with the principles of data protection legislation. 2 In particular, it shall ensure protection against fire, water, theft and unauthorised processing of the data. 29 Amended by No I of the O of 31 Oct. 2012, in force since 1 Jan. 2013 (AS 20126097). |
Art. 19a Electronic data carriers 30
1 The files transmitted in paper form shall be digitalised and stored in electronic form. Following digitalisation, the paper copies shall be destroyed. 2 The Federal Office may delegate these duties to an external agency, which undertakes in terms of a written agreement to record all the data electronically, treat it as confidential and guarantee its security. Article 9 of the Data Protection Act of 25 September 202031 applies mutatis mutandis.32 3 The Federal Office shall confirm on request that the digitalised documents correspond to their originals in paper form 30 Inserted by No I of the O of 31 Oct. 2012, in force since 1 Jan. 2013 (AS 20126097). 32 Second sentence amended by Annex 2 No II 90 of the Data Protection Ordinance of 31 Aug. 2022, in force since 1 Sept. 2023 (AS 2022 568). |
Art. 20 Archiving and destruction of the data 33
1 On expiry of the retention period of 80 years (Art. 26 of the Act), the data in the donor data register and the data under Article 15b paragraph 2 shall be offered to the Federal Archives for archiving. 2 The data regarded by the Federal Archives as not worthy of archiving shall be destroyed. 33 Amended by No I of the O of 31 Oct. 2012, in force since 1 Jan. 2012 (AS 2012 6097). |
Section 2 Procedure for Disclosure of Information |
Art. 21 Request for information
1 The child must submit to the Federal Office a written request for information in accordance with Article 27 paragraph 1 or 2, specifying the mother’s personal data. 2 The child must provide evidence of his or her identity in the form of a copy of a passport, identity card or an equivalent identity document and demonstrate that the requirements specified in Article 27 paragraph 1 or 2 of the Act are met.34 3 If the child is evidently incapable of acting on his or her own behalf, the Federal Office may request him or her to enlist a representative.35 34 Amended by No I of the O of 14 Nov. 2018, in force since 1 Jan. 2019 (AS 2018 4681). 35 Amended by No I of the O of 14 Nov. 2018, in force since 1 Jan. 2019 (AS 2018 4681). |
Art. 22 Notification of the sperm donor
1 If the child fulfils the requirements specified in Article 27 paragraph 1 or 2 of the Act and requests information on the personal data of the sperm donor, the Federal Office shall ascertain the latter’s current address. In doing so, the Federal Office shall as far as possible avoid indicating the purpose of the inquiry. 2 Federal, cantonal and communal authorities that can provide the relevant information are obliged to assist the Federal Office at its request. 3 The Federal Office shall inform the sperm donor of the fact that his personal data are to be disclosed to the child. It shall grant him an appropriate period to express his wishes concerning personal contact with the child. |
Art. 23 Provision of information to the child 36
1 If the requirements of Article 27 paragraph 1 or 2 of the Act are met, the child may choose whether to be provided information:
2 The personal details of the sperm donor shall be provided to the child in a written report. 3 If the requirement in Article 27 paragraph 1 of the Act is not met, the Office shall inform the child in writing that he or she is not yet entitled to be provided with information. 4 If the requirement in Article 27 paragraph 2 of the Act is not met, the Office shall inform the child in writing that he or she has no legitimate interest and, provided the requirement in Article 27 paragraph 1 of the Act is met, that he or she may choose how information is provided in accordance with paragraph 1. 5 The Office shall notify the child if the donor could not be found or could not be reliably identified, failed to answer or declined any personal contact. 6 It shall advise the child with regard to the counselling options available. 36 Amended by No I of the O of 14 Nov. 2018, in force since 1 Jan. 2019 (AS 2018 4681). |
Art. 2437
37 Repealed by No I of the O of 14 Nov. 2018, with effect from 1 Jan. 2019 (AS 2018 4681). |
Art. 26 Charges
The charges and expenses in the disclosure procedure shall be based on the Ordinance of 27 October 199938 on Civil Status Fees. |
Chapter 3 Final provisions |
Art. 28 Transitional provisions to the Amendment of 21 June 2017 40
1 Licence holders under Article 8 paragraph 1 letter a of the Act who are already using reproductive techniques when the Amendment of 21 June 2017 comes into force and who wish to continue with such activities must submit an application to the supervisory authority within three years containing proof that they meet the requirements under Article 4 paragraph 1 hereof. They may continue their activities until the decision of the supervisory authority takes full effect. 2 Licence holders under Article 8 paragraph 1 letter a of the Act who are already using reproductive techniques with analyses of genetic material from reproductive cells when the Amendment of 21 June 2017 comes into force and who wish to continue with such activities must submit an application to the supervisory authority within three years containing proof that they meet the requirements under Article 9 paragraph 3 of the Act and Articles 4 paragraph 1 and 6 paragraph 2 hereof. They may continue their activities until the decision of the supervisory authority takes full effect. 40 Amended by No I of the O of 21 June 2017, in force since 1 Sept. 2017 (AS 2017 3651). |
Annex 1 Annex 2 4142
41 Originally: Annex. Repealed by No II of the O of 31 Oct. 2012, with effect from 1 Jan. 2013 (AS 2012 6097). 42 Inserted by No II of the O of 21 June 2017, in force since 1 Sept. 2017 (AS 2017 3651). |
(Art. 4 para. 1 let. c) |
Quality management system |
European Standard ISO/IEC 17025:2005 (General Requirements for the Competence of Testing and Calibration Laboratories) or ISO 15189:2012 (Medical Laboratories – Requirements for Quality and Competence)43. 43 The standards may be inspected at the Federal Office of Public Health, Schwarzenburgstrasse 157, 3003Bern, or obtained from the Swiss Association for Standardisation, Sulzerallee 70, 8404Winterthur; www.snv.ch. |
Annex 3 44
44 Inserted by Annex 6 No II 2 of the O of 23 Sept. 2022 on Human Genetic Testing, in force since 1 Dec. 2022 (AS 2022 585). |
(Art. 2 para. 1bis and 1ter) |
Qualification requirements for using assisted reproductive techniques according to the state of the art |
Persons are qualified to use assisted reproductive techniques according to the state of the art if they hold:
45. |
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