Regulatory compliance is a necessity in the development of medical devices such as In Vitro Diagnostic (IVD) and Software as Medical Device (SaMD) to safeguard the health and safety of patients when used as intended. This is pivotal to an effective product life cycle management.
This workshop will build upon concepts on Design and Development and look into how manufacturing requirements are determined. These procedures are essential to ensure that products developed during the design phase can be manufactured, and contribute to the successful planning of product registration activities.
Due to the limited availability of seats, early registration is strongly recommended.
Click
here to find out more about the Fees.
The Centre of Regulatory Excellence is an accredited provider for Continuing Professional Education (CPE) for Pharmacists and Continuing Medical Education (CME) for Doctors.
Continuing education credits are available for CoRE events through the Singapore Pharmacy Council and the Singapore Medical Council subject to their respective approvals.
Attendees who wish to avail of the credits are required to sign the relevant registration form along with their CPE/CME number on the day of the events.Should the event be conducted online, please provide your CPE/CME number in the respective e-registration form.
The attendee’s registration details will be submitted after the event and credited upon receiving respective approvals.
Date and Time
23 Mar 2023 @ 08:30 - 24 Mar 2023 @ 17:30
Venue