Course not currently available

Medical Device Regulatory Affairs in Latin America

Course

In Harrington Hall Hotel, London ()

£ 1,150 + VAT

Description

  • Type

    Course

  • Duration

    2 Days

This seminar will provide a comprehensive overview of the requirements for successful product approval for medical devices in Latin America. The programme will cover the regulatory requirements but will also share the interpretation of the regulation, guidance and legislation in these countries that only someone with hands-on experience in the region can provide. It is anticipated that this seminar will be useful both as an introductory course and as a refresher to personnel who need to have up to date and global knowledge of the requirements in this geographical area. Suitable for: Medical Companies

Questions & Answers

Add your question

Our advisors and other users will be able to reply to you

Fill in your details to get a reply

We will only publish your name and question

Reviews

Course programme

Management Forum has had a portfolio of Life Science events running since 1983. We are at the cutting edge of information exchange, organising over 250 conferences, seminars and residential schools every year. All of our events are researched by our experienced course directors and designed to help you make informed decisions and remain up to date with 'need to know' business information.

Management Forum Conferences offer you the opportunity to network with colleagues in your area of business and our Seminars and Residential Schools provide an intimate, interactive environment in which to learn about the latest techniques and developments.

Take advantage of the whole range of Management Forum products to help you keep up-to-date on the latest developments within Pharmaceutical and associated industry sectors.

Management Forum have been running a fast developing and hugely successful MEDICAL DEVICE conference schedule for many years. During this time, major changes in device technology, delivery systems and regulatory requirements have occurred. These changes have all been reflected through 100’s of quality conferences and seminars as we continue to deliver up-to-date and topical information to the medical device industry.

This seminar will provide a comprehensive overview of the requirements for successful product approval for medical devices in Latin America. An ever increasing market, this is an excellent opportunity to learn the processes involved from an experienced consultant in this region. The programme will cover the regulatory requirements but will also share the interpretation of the regulation, guidance and legislation in these countries that only someone with hands-on experience in the region can provide. It is anticipated that this seminar will be useful both as an introductory course and as a refresher to personnel who need to have up to date and global knowledge of the requirements in this geographical area.

An addition to the programme this year will include a session on effective cross-cultural communication.

Medical Device Regulatory Affairs in Latin America

£ 1,150 + VAT