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GXP
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THE ROLE OF THE
RESPONSIBLE PERSON

MHRA Review on Good Distribution Practice

Conference Date: 14 Oct 2009-04 Dec 2009
Conference Ref: M10-6309
Fee: £660 + VAT
Venue: Harrington Hall Hotel, London

INTRODUCTION

Learn how to operate Good Distribution Standards under the Guidance of the UK MHRA Healthcare Regulations by following the Orange Guide.

WHO SHOULD ATTEND

This training course is aimed at:

  • RPs / QPs
  • Directors
  • Heads and Managers of:
  • Wholesale
  • Supply Chain Management
  • Logistics and Logistics Systems
  • Warehousing / Distribution
  • QA / QC
  • Planning and Forecasting
  • Transport / Packaging
  • Customer Demand Management
  • Inventory Management
  • Stock Control
  • Regulatory Affairs

Speakers

John Taylor - Quality and Standards Manager, Medicines and Medical Devices Regulator, Medicines and Healthcare products Regulatory Agency (UK MHRA)

Peter Blundell -Head of Regulatory Affairs and Quality ssurance, Lloyds Pharmacy, UK.

Tony Garlick - Technical Director for the British Association of Pharmaceutical Wholesalers (BAPW).

Presentation Topics:

  • The Role of the Regulator
  • Self Audits
  • Risk Based Inspections
  • Role of the Responsible Person
  • Responsibilities and Training
  • Supply Chain Review
  • Cold Chain Distribution
  • Ambient Temperature
  • Temperature Transits / Delivery Couriers
  • Track and Trace Products
  • EU Standardisation
  • Counterfeit Medicines

Interactive Workshops:

  • Standard Operation Procedures
  • Supply Chain Review
  • The Cold Chain / Ambient Temperature Monitoring
  • Counterfeit Management
  • Recalls
  • Role of the Responsible Person

Click here to book your place on this important Annual Event