Regulatory Affairs for Support Staff

Course

In London

£ 1,199 + VAT

Description

  • Type

    Seminar

  • Level

    Intermediate

  • Location

    London

  • Class hours

    8h

  • Duration

    2 Days

An Overview of Pharmaceutical Regulatory Affairs for Support Staff.
Key Topics to be be covered:-
Understand the Background of EU Law – Regulations, Directives and Guidelines
Discover where you can find Information on Regulatory Affairs, Approvals, Withdrawals etc
Assess the Impact of the EU Clinical Trials Regulation
Gain an Understanding of the Common Technical Document
Discuss how to Apply for a Marketing Authorisation in the EU – the Centralised, Decentralised and Mutual Recognition Procedures
Clarify Post Authorisation Obligations – Pharmacoviglance, Variations and Renewals

Facilities

Location

Start date

London
See map
11 Thurloe Place, SW7 2RS

Start date

On request

About this course

This two day course provides an introduction to Pharmaceutical Regulatory Affairs and the basics of drug development and has been designed specifically for those working in a support staff role. You will gain an overview of EU regulatory procedures required to register products in Europe and the regulatory activities that need to be complied with to keep products on the market. Pharmacovigilance and safety reporting will be covered as well as license variations and the commercial aspects of Pharmaceutical products. The course will provide a thorough grounding in the subject of Regulatory Affairs and enable you to perform in your role more effectively.

This course is specifically designed for anyone working in Regulatory Affairs, including personal assistants, secretaries, administrators and any member of support staff wishing to gain a greater understanding of Regulatory Affairs in the Pharmaceutical Industry. It is also suitable for those who interface with the Regulatory Affairs function and who provide support to the Regulatory procedures and activities.

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Reviews

Subjects

  • Staff
  • Directives etc
  • IT Law
  • EU Law
  • Clarify
  • Marketing
  • Law
  • Regulations

Teachers and trainers (1)

Norah Lightowler

Norah Lightowler

Lightowler Associates

Course programme

An Overview of Pharmaceutical Regulatory Affairs for Support Staff.

Key Topics to be be covered:-

  • Understand the Background of EU Law – Regulations, Directives and Guidelines
  • Discover where you can find Information on Regulatory Affairs, Approvals, Withdrawals etc
  • Assess the Impact of the EU Clinical Trials Regulation
  • Gain an Understanding of the Common Technical Document
  • Discuss how to Apply for a Marketing Authorisation in the EU – the Centralised, Decentralised and Mutual Recognition Procedures
  • Clarify Post Authorisation Obligations – Pharmacoviglance, Variations and Renewals
WHY YOU SHOULD ATTEND

This two day course provides an introduction to Pharmaceutical Regulatory Affairs and the basics of drug development and has been designed specifically for those working in a support staff role. You will gain an overview of EU regulatory procedures required to register products in Europe and the regulatory activities that need to be complied with to keep products on the market. Pharmacovigilance and safety reporting will be covered as well as license variations and the commercial aspects of Pharmaceutical products. The course will provide a thorough grounding in the subject of Regulatory Affairs and enable you to perform in your role more effectively.

Regulatory Affairs for Support Staff

£ 1,199 + VAT