+353 89 9680794
Dublin, Ireland
In-Person
Visio
Moday, 6 Jan 2025 (09:00 AM) - Wednesday, 8 Jan 2025 (05:00 PM) Caucasus Standard Tim
Centre International des Conférences Abdelatif-Rahal
We are delighted to be able, as the first Platform regulatory in Algeria, to strengthen the criteria for approving medical products, medicines for human use and adaptive medical devices, and to obtain brand recognition in Algeria from the source directly .
Robust regulatory provisions in line with international standards are essential to ensure the short-term availability of high-quality medical products in countries where consumption is low or average. By harmonizing criteria throughout Algeria, we will be able to improve patient access to high-quality medical technologies and, at the same time, facilitate market access for innovators.
This first edition of the conference offers manufacturers and suppliers a common platform to identify opportunities for introducing better performing products to the Algerian market.
The Medtech Reg Medical devices Algeria summit will highlight critical medical products and in vitro diagnostic tests and will feature case studies, interactive presentations and in-depth discussions with the ANPP and the Ministry of Health.
Participants are invited to actively participate in the development of leading regulatory strategies for bringing products to the Algerian market.
Join us as we the first international Regulatory Affairs to navigate the intricacies of Medical Device,SamD and IVD Regulations, and facilitate market access across Algeria.
Robust regulatory frameworks, aligned with international standards, are pivotal in ensuring widespread availability of high-quality medical devices in low- and middle-income nations. By harmonizing regulations across Algeria , we can simplify market entry for innovators, ultimately enhancing patient access to safe medical technologies.
Over two days, this event offers a collaborative platform for manufacturers and distributors to explore avenues for introducing life-changing devices into the Algerian market.
Medtech algeria event will highlight critical medical device and IVD regulations, leveraging case studies, interactive presentations, and engaging discussions with AMPP and ministry of health .
Attendees will gain valuable insights into tailored regulatory strategies for product placement across Algeria markets. Don’t miss this opportunity to navigate the evolving landscape of medical device regulation and drive impactful change across the continent.
Early Bird Rate (before 10 December 2024) | Regular Rate (after 10 December 2024) | |
Mecomed and RAPS members | AED 920 / USD 250 | AED 1285 / USD 350 |
Government | AED 0 / USD 0 | AED 0 / USD 0 |
Non-members | AED 1285 / USD 350 | AED 1650 / USD 450 |
For more information about registration as a member of the press, contact us today
at contact@smartqara.com
Subject to change without notice.
Credit card payments (MasterCard and Visa are accepted through the online registration system. There is an option to pay by bank transfer.
You will receive a confirmation after successfully submitting your registration. Email registration at MMTRS@InfoPlusEvents.com if you have not received the email confirmation. Registration received without payment will not be processed.
All cancellation requests must be submitted in writing to MMTRS@InfoPlusEvents.com and raps@raps.org. Cancellations received by 27 December 2024 will receive a full refund minus a 20% administrative fee. Cancellations received after 27 December 2024 are nonrefundable except in cases of documented medical emergencies. We are unable to accept cancellations by phone. The organizers reserve the right to cancel this program at their sole discretion in which case registration fees will be refunded within 7 business days. The organizers will not be responsible for travel or other costs incurred due to cancellation.
To substitute the registration, email MMTRS@InfoPlusEvents.com and raps@raps.org. The email should from the registered email ID with the details of the below details of the substitute:
The Medtech Reg Medical devices Algeries summit is a 2-Day enriched summit that serves as a strategic meeting place for Algeria and international biotechnology l industry professionals where all stakeholders present share insights, discuss the latest regulatory updates, and engage in knowledge-sharing sessions to support the growth of Medical devices regulatory affairs,and compliance sectors in Algeria.
Topic 1 Market Access with Ministery of health
Topic 2 Regulatory requirements
Topic 3 MDR impact
Topic 4 labeling according to Algerian market
Topic 5 Sterilization summary
Topic 6 Risk management plan
Topic 7 clinical report
Topic 8 PMS
Topic 9 workshop for iso 13485
Topic 10 MDR
Details and agenda will follow two weeks before the summit
Audio or video recordings of the event is prohibited.
By registering for this event, you grant full permission to the organizers to capture, store, use, and/or reproduce your image or likeness, photograph, voice, biographical information, comments, persona, writings and/or personal property recordings, including incidental capture of any individuals in your household or workplace by any audio and/or visual recording technique and use such content in any and all media or forms by Mecomed, RAPS, InfoPlus Events LLC or third parties without compensation or notice, including for promotional or advertising purposes. You also waive any right to royalties or other compensation arising from or related to the use of the images, recordings, or materials. By registering, you release, defend, indemnify, and hold harmless Mecomed, RAPS and InfoPlus Events LLC from and against any claims, damages, or liability arising from or related to the use of the images, recordings, or materials, including but not limited to claims of defamation, invasion of privacy, or rights of publicity or copyright infringement, or any misuse, distortion, blurring, alteration, optical illusion, or use in composite form that may occur or be produced in taking, processing, reduction, or production of the finished product, its publication, or distribution.
By registering for this event, you provide consent that your profile will be stored with RAPS and Mecomed and shared with processors for the purpose of doing business with RAPS and Mecomed for this event. You consent to receiving announcements from RAPS and Mecomed and that you can opt-out at any time by contacting the respective organization or updating preferences. You understand that your demographic information captured will be used to update your profile in the RAPS and Mecomed databases.
You also provide consent to be added to a related online community on RAPS Regulatory Exchange at connect.raps.org, powered by Higher Logic for networking and related resources and announcements regarding this event. You may opt out at any time on connect.raps.orYou are also aware that your name and mailing address will be provided to event exhibitors and sponsors and company and title may be shared with speakers and that you may opt out of communications with them at any time by directly contacting them.
You understand that RAPS and Mecomed may use your email address to identify you on social media outlets for the purpose of sharing information of RAPS and Mecomed products and services and for information related to this transaction. You understand you can modify my privacy settings on these outlets directly. You also understand that you can opt-out of RAPS and Mecomed identifying me on these outlets by contacting the appropriate organization.
The programme for this summit is carefully curated by experts across the medtech community to ensure the highest quality discussions, knowledge exchange, and collaboration opportunities. We thank them for their hard work and dedication to this important event.
Founder/Executive Consultant, AKRA TEAM
Growth Emerging Markets (GEM) Regulatory Lead, Boston Scientific Middle East FZ LLC
Regulatory Affairs Director, Mecomed
Vice President Regulatory Affairs EMEA, LATAM, Canada, Edwards Life Sciences
Vice President Regulatory Affairs EMEA and Canada, Johnson & Johnson
Senior Vice President Global Regulatory and Quality, Medical Devices, BSI
Partner, Axon Lawyers
Packages are now available to support the 2025 MEA MedTech Regulatory Summit, presented by Mecomed and RAPS. We thank you in advancing for making the commitment to join us as we unite senior decision makers and regulators across the medical device community to ensure that regulatory professionals are able to stay up-to-date and navigate complexities during an era of rapid change.
Contact us on email contact@smartqara.com
SMART QARA is a project agency specialized in the life science industry. Our focus is on providing highly qualified services, we target an extensive network in the EU region and beyond.
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