MANAGEMENT FORUM'S PHARMACEUTICAL CONFERENCES AND SEMINARS

For more information or to contact Sarah Spanswick, Conference Director, click here

DATE	CONFERENCE

24-25 May 2012	UNDERSTANDING THE BASICS OF EU REGULATORY AFFAIRS How to optimise your drug submission procedures
31 May 2012	THE EU EVMPD LATEST UPDATE Will you be Compliant by 2 July 2012
07-08 Jun 2012	CLINICAL TRIAL REGULATORY AND GUIDELINE REQUIREMENTS Including an update on the proposed change to the EU Clinical Trial Directive requirements
18-19 Jun 2012	PROJECT MANAGEMENT FOR PHARMACEUTICAL PROFESSIONALS Two day interactive course
19-21 Jun 2012	PHARMACOVIGILANCE A Basic Training Course For Those Working On Drug Safety Monitoring in the EU, USA and Japan
19-20 Jun 2012	AN ESSENTIAL GUIDE TO CONTINUING MEDICAL EDUCATION (CME) Supported by European CME Forum
19-20 Jun 2012	DRY POWDER INHALERS Key Annual Conference for Pharmaceutical and Medical Device Professionals in the DPI Market
21-22 Jun 2012	EDITING SCIENTIFIC MEDICAL TEXTS
29 Jun 2012	NEW PHARMACOVIGILANCE LEGISLATION ~DIRECTIVE 1235/2010 AND 2010/84 July 2012 ~ ALL CHANGE FOR EUROPE Are you prepared for the new legislation?
02-05 Jul 2012	PHARMA MINI MBA A 4 Day Accelerated Management Programme
02 Jul 2012	WEBINAR - NEW PHARMACOVIGILANCE LEGISLATION Are You Prepared
04 Jul 2012	NEW PHARMACOVIGILANCE LEGISLATION ~ DIRECTIVE 1235/2010 AND 2010/84 July 2012 ~ ALL CHANGE FOR EUROPE Are you prepared for the new legislation?
04 Jul 2012	THE EU COSMETICS DIRECTIVE AND THE COSMETICS REGULATIONS All You Need to Know to Market a Cosmetic Product in Europe
17-18 Jul 2012	CERTIFIED PATENT VALUATION ANALYST COURSE to be held in Zurich In association with The Business Development Academy
20-21 Aug 2012	NEW PHARMACOVIGILANCE LEGISLATION ~ DIRECTIVE 1235/2010 AND 2010/84 July 2012 ~ ALL CHANGE FOR EUROPE
10-12 Sep 2012	STRATUM CORNEUM VII www.stratumcorneum2012.com
17-18 Sep 2012	GAINING REGULATORY APPROVAL FOR EU AND US BIOLOGICS
17 Sep 2012	HOW TO WRITE SOPs
18 Sep 2012	IMPROVING PROCESSES AND CAPA (Corrective and Preventative Action)
19 Sep 2012	IMPACT OF THE NEW PHARMACOVIGILANCE LEGISLATION
20-21 Sep 2012	INTRODUCTION TO MANUSCRIPT WRITING Two Day Intensive Course
24 Sep 2012	ESSENTIAL GUIDE TO PHARMACOVIGILANCE
26-28 Sep 2012	BIOTECHNOLOGY FOR THE NON BIOTECHNOLOGIST Comprehensive three day course
27 Sep 2012	THE CLINICAL OVERVIEW AND CLINICAL SUMMARY
28 Sep 2012	UNDERSTANDING THE DECENTRALISED AND MUTUAL RECOGNITION PROCEDURES
02-03 Oct 2012	PS 9000-2011 IN THE PHARMACEUTICAL SUPPLY CHAIN Standards for Pharmaceutical Packaging Materials and Components: New Requirements and Implications
03-05 Oct 2012	SUCCESSFUL MEDICAL WRITING
	REGULATORY AFFAIRS IN AFRICA ~ INCLUDING SOUTH AFRICA This meeting has been postponed until Autumn 2012
	PHARMACEUTICAL PACKAGING AND LABELLING ~ 2 Day Webcast The Challenges and Solutions
	ONLINE EXAM - CERTIFICATE IN GCP & EU CLINICAL TRIAL DIRECTIVE ONLINE EXAM