Regulation of software a medical device

Transcription

1 Regulation of software a medical device IOF-TTO Event Steve Eglem Responsible of clinical famhp Member of the medical device European Clinical and Evaluation (CIE) working group

2 Content Famhp presentation European and Belgian legal framework on medical devices Legal reference Definitions & Examples Classification Software as medical device Validation process and conformity assessment Impact of MDR Impact of GDPR from medical device perspective Subject - Date FAMHP/entity/Division-Unit-Cell 2

3 Who are we? FAMHP - AFMPS FAGG Address : Victor Horta Square 40/40 In front of the Midi Station More than 400 employees Minister of Public Health and Social Affairs : Maggie De Block CEO : Xavier De Cuyper 3

4 FAMHP National competent autority in Belgium responsible for the quality, safety and efficacy of medicines and health products. The famhp ensures, from development to use, the quality, safety and efficacy of medicines for human and veterinary use (including homeopathic medicines, herbal medicines, pharmacy made and officinal preparations) and also medical devices and accessories, and raw materials for the preparation and production of medicines. From collection to use, the fahmp ensures the quality, safety and efficacy of all the operations involving with blood, cells and tissues. Our stakeholders : 4

5 Legal framework 93/42 directive : MD NMR, US, X-ray, Hip-implants, ECG, EEG, Intravascular catheters, Stents, syringes, IOL, RR, med. lasers, med. software 90/385 directive : AIMD Pacemakers; ICD s Implantable Infusion pumps Artificial hearts... 98/79 directive : IVD MD HIV-tests, Hepatitis-tests, Pregnancy-tests, Lab-Automats, Reagents, Calibrators, Control materials Prim. specimen receptacles... Transpositions RD 18/03/1999 RD 15/07/1997 RD 14/11/2001 5

6 Legal framework Future 93/42 directive : MD NMR, US, X-ray, Hip-implants, ECG, EEG, Intravascular catheters, Stents, syringes, IOL, RR, med. lasers, med. software 90/385 directive : AIMD Pacemakers; ICD s Implantable Infusion pumps Artificial hearts... 98/79 directive : IVD MD HIV-tests, Hepatitis-tests, Pregnancy-tests, Lab-Automats, Reagents, Calibrators, Control materials Prim. specimen receptacles... Regulation 2017/745 Regulation 2017/746 6

7 Legal framework Definition medical device means any instrument, apparatus, appliance, software, material or other article, whether used alone or in combination, including the software intended by its manufacturer to be used specifically for diagnostic and/or therapeutic purposes and necessary for its proper application, intended by the manufacturer to be used for human beings for the purpose of: diagnosis, prevention, monitoring, treatment or alleviation of disease, diagnosis, monitoring, treatment, alleviation of or compensation for an injury or handicap, investigation, replacement or modification of the anatomy or of a physiological process, control of conception, and which does not achieve its principal intended action in or on the human body by pharmacological, immunological or metabolic means, but which may be assisted in its function by such means; 7

8 MD 8

9 Legal framework Definition 'active medical device' means any medical device relying for its functioning on a source of electrical energy or any source of power other than that directly generated by the human body or gravity, Stand alone software with a medical purpose is considered as an active medical device 9

10 Legal framework Definition 'active implantable medical device (AIMD) means any active medical device which is intended to be totally or partially introduced, surgically or medically, into the human body or by medical intervention into a natural orifice, and which is intended to remain after the procedure; 10

11 Legal framework Definition AIMD 11

12 Legal framework Definition accessory means an article which whilst not being a device is intended specifically by its manufacturer to be used together with a device to enable it to be used in accordance with the use of the device intended by the manufacturer of the device; 12

13 Legal framework Definition Example : Accessory of ECG machine : pads, paper. 13

14 Legal framework Definition Example : Accessory of medical contact lens : liquid to wash/rince the lens 14

15 Legal framework Definition Example : Accessory of medical endoscope : screen monitors, cables, 15

16 Legal framework Definition Example : Accessory of medical endoscope : disinfecting solution 16

17 in vitro diagnostic medical device (IVD) means any medical device which is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, equipment or system, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue donations, derived from the human body, solely or principally for the purpose of providing information: concerning a physiological or pathological state, or concerning a congenital abnormality, or to determine the safety and compatibility with potential recipients, or Legal framework Definition to monitor therapeutic measures. 17

18 IVD 18

19 MD 19

20 Legal framework Classification Rules of classification based on the potential risks associated with the technical design and manufacture of the devices From medtech Europe 20

21 Legal framework Classification (from software perspective) EU Directive No specific rules of classification (follow active medical devices) MDR Specific classification for software : providing information which is used to take decisions with diagnosis or therapeutic purposes (Class IIA/IIB/III) Intended to monitor physiological processes (Class IIB) Others (Class I) 21

22 Legal framework Software as medical device Could fall under IVD or MDD directive Medical purpose (claim!) Software does not perform an action on data, or performs an action limited to storage, archival, communication, "simple search" or lossless compression. And if my app falls under a medical device framework? It must comply with the safety and performance requirements Other obligations for manufacturers regard the issues of registration, post-market surveillance, incident reporting. 22

23 Legal framework Software as medical device 23

24 Legal framework Software as medical device 24

25 Validation process and conformity assessment What does it mean? Demonstrate the safety and performance of the device. Performance : The ability of a medical device to achieve its intended purpose as claimed by the manufacturer. Safety : The absence of unacceptable clinical risks, when using the device according to the manufacturer s Instructions for Use. Device fulfill essential requirements? the information materials supplied by the manufacturer (the labelling, instructions for use, promotional materials, including accompanying documents foreseen by the manufacturer) the clinical evaluation (the device description used for the clinical evaluation, other contents of the clinical evaluation report) the available clinical data (such as results of Clinical Investigations, publications, PMS studies, etc.). 25

26 Validation process and conformity assessment Clinical Evaluation : From the beginning (development of the device) Mandatory for CE-marking Updated throughout all the life cycle of the device (pre and post market) Guide the clinical research (with the risk management; iso Preclinical Data Scientific litterature Similar product? Check harmonized standards, what is needed? Biocompatibility tested Fatigue and resistance test Build your risk analysis during each step Essential requirements Demonstration of conformity is now fulfilled? Clinical Data Scientific litterature Clinical Investigation Sufficient clinical evidence? Performance (claim!) safety 26

27 Validation process and conformity assessment Essential requirements (ER) in the current directive : Annex I point 12. Requirements for medical devices connected to or equipped with an energy source : repeatability, reliability and performance of these systems according to the intended use validated according to the state of the art taking into account the principles of development lifecycle, risk management, validation and verification. Monitor clinical parameters : alarm should be implemented Cybersecurity not included in the current directive Standards for software which could provide more information on the ER that you need to fulfill and how to do it: IEC : medical software software life-cycle processes NBN : Medical devices - Application of usability engineering to medical devices NBN : Health Software - General requirements for product safety 27

28 Validation process and conformity assessment Conformity procedure? Different routes following the MD classification Such compliance must be assessed through a specific conformity assessment procedure, which is proportional to the risk-class: For low-risk products (Class I), the manufacturer can provide a self-declaration For all other products (Classes IIa, IIb and III), a control must be done by a Notified Body 28

29 Validation process and conformity assessment Conformity procedure? 29

30 Impact of MDR 30

31 Impact of MDR/IVDR The new Regulations contain a series of extremely important improvements to modernise the current system. Among them are: stricter control for high-risk devices the reinforcement of the criteria for designation and processes for oversight of Notified Bodies the inclusion of certain aesthetic devices which present the same characteristics and risk profile as analogous medical devices under the scope of these Regulations (annex XVI) the introduction of a new risk classification system for in vitro diagnostic medical devices in line with international guidance improved transparency through an European database 31

32 Impact of MDR/IVDR the reinforcement of the rules on clinical evidence, including an EU-wide coordinated procedure for authorisation of multi-centre clinical investigations the strengthening of post-market surveillance requirements for manufacturers improved coordination mechanisms between EU countries in the fields of vigilance and market surveillance Existing products will have to be reassessed under the new rules at latest may 2024 New definitions Introduction of Common Specifications (CS): a set of technical and/or clinical requirements other than a standard, providing a means to comply with the legal obligations applicable to a device, process or system 32

33 Impact of GDPR Article 110 of MDR: Member States shall apply Directive95/46/EC to the processing of personal data carried out in the Member States pursuant to this Regulation Directive 95/46/EC is replaced as from 25 May 2018 by Regulation 2016/679 (EU) of 27 April 2016 on the protection of natural persons with regard to the processing of personal data («GDPR») Health-related data not defined in current Directive GDPR: data concerning health = Personal Data related to Physical or mental health Of a (identified or identifiable) natural person Including the provision of health care services Which reveals information about his/her health status Large definition Impact on clinical investigation to collect clinical data Advice from ethic committee 33 33

34 Take home message Your claim, purpose, objective of your app Apply the regulatory route Possible medical device Check it with EU guidance, ask to a competent autority Plan your clinical evaluation taking into account the new regulation from now! 34

35 Contact Federal Agency for Medicines and Health Products FAMHP Place Victor Horta 40/ BRUXELLES tel fax welcome@fagg-afmps.be 35

36 Tools 36

37 Tools 37

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39 Tools 39

40 Your medicines and health products, our concern