Presented by
Management Forum
Sterile devices are free of viable microorganisms and sterilization is one of the key processes in the production of sterile medical devices. Regulations for medical devices include particular requirements for devices supplied or intended to be used in a sterile state. These regulatory requirements relate to general safety and performance aspects for the products, and the requirements for independent, third-party conformity assessment of the processes for achieving sterility. Evidence of successful sterilization is important and expected when demonstrating conformity with the regulations. This course provides a comprehensive overview of these regulatory requirements and how to comply, together with the science and standards that support them.
★★★★★ "[Speaker] very experienced, knowledgeable and approachable. Webinar [was] prepared taking into accou... more"
3-4 February 2025
+ 5-6 June 2025, 16-17 October 2025 »
from £1299
Sterile devices are free of viable microorganisms and sterilization is one of the key processes in the production of sterile medical devices. Regulations for medical devices include particular requirements for devices supplied or intended to be used in a sterile state. These regulatory requirements relate to general safety and performance aspects for the products, and the requirements for independent, third-party conformity assessment of the processes for achieving sterility. Evidence of successful sterilization is important and expected when demonstrating conformity with the regulations.
These requirements have been supported by a portfolio of standards on:
This course provides a comprehensive overview of these regulatory requirements and how to comply, together with the science and standards that support them.
Please note that delegates will require access to copies of ISO 11135 and ISO 11137-1 in order to take part in the exercises. If you do not already have access to these through your organisation, please see below the ways to acquire them:
ISO 11135 - https://www.iso.org/standard/56137.html
ISO 11137-1 - https://www.iso.org/standard/33952.html and amendment at https://www.iso.org/standard/72106.html
These standards are also available from national standards organizations such as BSI, DIN, AFNOR, AAMI, NSAI, etc.
This course is part of our GxP training (Good x Practice) course collection, which features a variety of topic areas to ensure you comply with the most recent quality guidelines. For more information on the latest EU GMP regulations, see our GMP training course covering the Annex 1.
A quality management professional, chartered biologist and member of the Royal Society of Biology, with over 35 years’ experience in the medical device, pharmaceutical, biotechnology and food industries. Extensive knowledge of quality and environmental management systems, internal and third-party auditing and personnel training. Eligible to act as a Qualified Person as defined in Directive 2001/83/EC, as amended (previously 75/319 et al.) since 1993. A Qualified Notified Body Lead Auditor since 2002 (IRCA ref: 1182641).
NEW higher discounts for multiple bookings - bring your colleagues to make your training budget go further:
Please contact us for pricing if you are interested in booking 5 or more delegates
3-4 February 2025
Live online
09:30-17:30 UK (London) (UTC+00)
10:30-18:30 Paris (UTC+01)
04:30-12:30 New York (UTC-05)
Timings may be different for each day
Course code 14477
Until 30 Dec
Not ready to book yet?
for 7 days, no obligation
5-6 June 2025
Live online
09:30-17:30 UK (London) (UTC+01)
10:30-18:30 Paris (UTC+02)
04:30-12:30 New York (UTC-04)
Timings may be different for each day
Course code 14730
Until 01 May
Not ready to book yet?
for 7 days, no obligation
16-17 October 2025
Live online
09:30-17:30 UK (London) (UTC+01)
10:30-18:30 Paris (UTC+02)
04:30-12:30 New York (UTC-04)
Timings may be different for each day
Course code 15022
Until 11 Sep
Not ready to book yet?
for 7 days, no obligation
* Early booking discounts may not be combined with other discounts or offers. As such, the discounts for 2nd/3rd/4th delegates are based on the full price; and apply only when booking multiple delegates on the same date.
[Speaker] very experienced, knowledgeable and approachable. Webinar [was] prepared taking into account all of the participants with the general information as well as with the direct individual requirements in mind. Questions answered at the time as well as within time given after the webinar. Thank you.
Oct 17 2024
Dorota Seweryn
Quality Engineer, First Water Ramsbury Limited
Jun 6 2024
The Speaker was very knowledgeable and the inside stories are great!
Priya Woodun
Senior QA Compliance Officer, Endomagnetics Ltd
Jun 1 2023
Very structured training at perfect pace, covering all important point. Very good interaction.
Marijana Jelecevic Kakouros
RA Manager, Beckton Dickinson
Oct 19 2023
Training materials were detailed and easy to follow. Trainer was engaged and made sure that contents were delivered in a way that the Trainees could relate to.
Esther Okeudo
QA Specialist, JenaValve
Jun 1 2023
An excellent webinar that delivered above and beyond. Eamonn would be a great contact to keep for the future. His knowledge is top class.
Kerry Poole
Mercian Surgical Co Ltd
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2 days
Typical duration
Pricing from:
We can customise this course to your requirements and deliver it on an in-house basis for any number of your staff or colleagues.
Contact our in-house training experts Aleksandra Beer and Yesim Nurko to discuss your requirements:
Multiple colleagues? See above for details of our discounts for 2, 3, or 4 delegates. For more, talk to one of our training experts to discuss how to: