Why You Need to Take This Training Course?
This Course will Provide YOU with three Benefits:
Comprehensive Understanding: Upbeat Consult’s training course provides a thorough understanding of medical device regulatory affairs and registration processes. Participants gain insights into the intricate frameworks governing medical device approvals, ensuring they are equipped with up-to-date knowledge and regulatory compliance expertise.
Enhanced Career Opportunities: Completion of the training course enhances career prospects within the medical device industry. With regulatory compliance being a critical aspect of product development and market entry, individuals with specialized training in regulatory affairs are highly sought after by medical device companies, regulatory bodies, and consulting firms. The certification from Upbeat Consult serves as a valuable credential, demonstrating proficiency in navigating complex regulatory landscapes.
Risk Mitigation and Compliance Assurance: By attending the training course, professionals learn strategies to mitigate regulatory risks and ensure compliance throughout the product lifecycle. This knowledge is indispensable for organizations seeking to bring innovative medical devices to market efficiently while adhering to regulatory requirements. Participants gain insights into best practices for regulatory submissions, quality management systems, and post-market surveillance, empowering them to contribute effectively to their organizations’ regulatory strategies and objectives.
What you'll learn
- Participants will have greater insight into the overall regulatory process of registering medical device in Europe and obtaining a CE mark
- Participants will become better knowledgeable in medical device classification and understanding the quality management ISO 13485 related to CE mark certification
- Participants will know the different the requirements for registration & clearance of Medical device in different Middle East countries such as Saudi, Jordan, UAE etc., in addition to:
- Requirement for Registration of Medical Device in a Pharmaceutical Presentation or Containing Drugs
- Surgical sutures; absorbable and non absorbable
- Variation to Registered Medical Device Products
This 8-hour Training Course is Equivalent to 7 Continuing Professional Development (CPD) hours.
- Duration: 8 Hrs. One Day
- Time: 9.00 am-4.00 pm
- Prerequisite for this course: None
- Language: English
- Level: Any one interested
- Classroom & Virtual Training
- Price US $ 320
- Certified and Accredited Certificate
- Discount available for companies who send three or more participants
- Seats for this course: 12
- Virtual through google meet
- Classroom course at Upbeat office, hotel or at the customer premises