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DATE TITLE SECTOR
15 Mar 2010 MEDICAL DEVICE CLINICAL INVESTIGATIONS AND EVALUATIONS Medical Devices
15 Mar 2010 GLOBAL MANUFACTURING SITE TRANSFER Pharmaceutical
17 Mar 2010 CLAIM AND SPECIFICATION DRAFTING FOR A SINGLE EPO/USPTO PATENT APPLICATION ~ London IP
18 Mar 2010 GUIDE TO THE FORMAL REQUIREMENTS OF THE EUROPEAN PATENT SYSTEM IP
19 Mar 2010 PATENT INFRINGEMENT: DOCTRINES OF EQUIVALENTS AND PURPOSIVE CONSTRUCTION IN US, UK AND GERMANY IP
22 Mar 2010 INJECTABLE DRUG DELIVERY - Devices, Technology & Development Medical Devices
22 Mar 2010 INTELLECTUAL PROPERTY IN THE PHARMACEUTICAL INDUSTRY IP
22 Mar 2010 ADVANCED PHARMACOVIGILANCE Pharmaceutical
23 Mar 2010 DRAFTING EFFECTIVE PHARMACEUTICAL CLAIMS WITH AN EYE TOWARDS THE USFDA ORANGE BOOK IP
24 Mar 2010 POST CONFERENCE WORKSHOP ON DRUG / DEVICE & DEVICE / DRUG COMBINATION PRODUCTS IN THE EU Medical Devices
25 Mar 2010 REGULATORY AFFAIRS FOR SUPPORT STAFF ~ PART 1 Support Staff Development
26 Mar 2010 REGULATORY AFFAIRS FOR SUPPORT STAFF ~ PART 2 Support Staff Development
12 Apr 2010 AN ESSENTIAL GUIDE TO PHARMACOVIGILANCE Pharmaceutical
14 Apr 2010 NASAL DRUG DELIVERY Medical Devices
14 Apr 2010 BIOTECHNOLOGY FOR THE NON-BIOTECHNOLOGIST GxP
14 Apr 2010 CLAIM AND SPECIFICATION DRAFTING FOR A SINGLE EPO/USPTO PATENT APPLICATION ~ Florida, USA IP
19 Apr 2010 STRATEGIES FOR MANAGING YOUR PATENT PORTFOLIO IP
21 Apr 2010 GOOD ENGINEERING PRACTICE: (GEP) GxP
22 Apr 2010 FORMALITY PROCEDURES FOR THE USPTO IP
22 Apr 2010 US FDA INSPECTION READINESS GxP
23 Apr 2010 PHARMACOVIGILANCE FOR SUPPORT STAFF Support Staff Development
23 Apr 2010 THE SUMMARY OF PRODUCT CHARACTERISTICS: CONSTRUCTION & HARMONISATION Pharmaceutical
26 Apr 2010 QUALITY MANAGEMENT SYSTEMS Medical Devices
26 Apr 2010 MANAGING THE LEGAL ASPECTS OF MULTI-NATIONAL CLINICAL TRIALS Legal
26 Apr 2010 CLINICAL AND POST MARKETING SAFETY Pharmaceutical
27 Apr 2010 SUCCESSFUL IMPLEMENTATION OF MANUFACTURING SITE TRANSFERS GxP
27 Apr 2010 IN-VITRO DIAGNOSTICS Medical Devices
28 Apr 2010 ANCILLARY MEDICINAL SUBSTANCES Medical Devices
29 Apr 2010 OWN BRAND LABELLING, SYSTEMS AND PROCEDURE PACKS Medical Devices
29 Apr 2010 BASIC PCT FORMALITIES COURSE IP
29 Apr 2010 THE PRACTICE OF ORAL PROCEEDINGS AT THE EUROPEAN PATENT OFFICE IP
29 Apr 2010 TRAIN THE PHARMACEUTICAL TRAINER Pharmaceutical
30 Apr 2010 MANAGING MEDICAL DEVICE SOFTWARE PROJECTS Medical Devices
30 Apr 2010 INTERNATIONAL REGISTRATION OF DESIGNS IP
06 May 2010 LATEST DEVELOPMENTS IN PHARMACOVIGILANCE Pharmaceutical
06 May 2010 INTRODUCTION TO THE MEDICAL DEVICE DIRECTIVES Medical Devices
10 May 2010 PHARMACOKINETICS In Drug Discovery and Development Pharmaceutical
14 May 2010 DESIGNING AROUND VALID US PATENTS IP
16 May 2010 PHARMACY IN PRACTICE Pharmaceutical
17 May 2010 SCIENCE IN PHARMACY Pharmaceutical
18 May 2010 REGULATORY AFFAIRS IN AFRICA including SOUTH AFRICA Pharmaceutical
19 May 2010 US PATENT PRACTICE IP
20 May 2010 TECHNOLOGY LICENSING Legal
20 May 2010 AN ESSENTIAL GUIDE TO CLINICAL TRIAL REGULATIONS Pharmaceutical
20 May 2010 EFFECTIVE PROJECT MANAGEMENT FOR MEDICAL WRITERS Pharmaceutical
21 May 2010 EDITING SCIENTIFIC AND MEDICAL TEXTS Pharmaceutical
24 May 2010 THE PATENT ASSERTION FORUM IP
24 May 2010 DRUG DELIVERY COMBINATION PRODUCTS - PRE-CONFERENCE WORKSHOP Medical Devices
25 May 2010 PRE-FILLED SYRINGES AND ADVANCED INJECTION TECHNOLOGIES Medical Devices
26 May 2010 THE PHARMA MINI MBA ~ MANAGEMENT FORUM'S SPRING SCHOOL Pharmaceutical
26 May 2010 THE EU PHARMACEUTICAL DOSSIER - CTD MODULES 2.3 and 3 Pharmaceutical
28 May 2010 MEDIA LAW Legal
30 May 2010 PHARMACEUTICAL REGULATORY AFFAIRS IN THE MIDDLE EAST Pharmaceutical
03 Jun 2010 OBTAINING AND ENFORCING US PATENTS IN A PATENT-HARSH ENVIRONMENT IP
08 Jun 2010 INTRODUCTION TO CONTRACTS Legal
11 Jun 2010 IP FORMALITIES MANAGEMENT IP
14 Jun 2010 INTRODUCTORY OVERVIEW OF THE PHARMACEUTICAL INDUSTRY Pharmaceutical
14 Jun 2010 WORKING THROUGH VETERINARY DRUG DEVELOPMENT Animal Health
14 Jun 2010 EUROPEAN MARKETING CODES AND COMPLIANCE Pharmaceutical
14 Jun 2010 WORKING WITH PATENTS ~ Management Forum's Patent Summer School IP
15 Jun 2010 THE EU COSMETICS DIRECTIVE AND THE NEW COSMETIC REGULATIONS Pharmaceutical
15 Jun 2010 PHARMACEUTICAL PACKAGING GxP
17 Jun 2010 FDA INSPECTIONS FOR MEDICAL DEVICES Medical Devices
21 Jun 2010 PHARMACOVIGILANCE Pharmaceutical
22 Jun 2010 PHARMACEUTICAL REGULATORY AFFAIRS IN CANADA Pharmaceutical
24 Jun 2010 OVERVIEW OF GCP Pharmaceutical
24 Jun 2010 PHARMACOEPIDEMIOLOGY Pharmaceutical
24 Jun 2010 MANAGING US LITIGATION FOR EUROPEAN COUNSEL Legal
25 Jun 2010 LATEST DEVELOPMENTS IN GCP Pharmaceutical
29 Jun 2010 IMPURITIES, IMPURITIES, IMPURITIES - 10th Annual Update Pharmaceutical
30 Jun 2010 DRY POWDER INHALERS Medical Devices
01 Jul 2010 HOW TO WRITE SOPs Pharmaceutical
01 Jul 2010 EU PHARMACEUTICAL REGULATIONS - For the Pharmaceutical and Biotechnology Industries Pharmaceutical
02 Jul 2010 IMPROVING PROCESSES AND CAPA (CORRECTIVE AND PREVENTATIVE ACTION) Pharmaceutical
05 Jul 2010 MANAGEMENT FORUM'S MEDICAL DEVICE SUMMER SCHOOL - 5 Day Residential Course - London Medical Devices
08 Jul 2010 MICROBIOLOGICAL ISSUES IN PHARMACEUTICAL PRODUCTION AND CONTROL GxP
26 Jul 2010 WORKING THROUGH DRUG DEVELOPMENT - MANAGEMENT FORUM'S SUMMER SCHOOL Pharmaceutical
07 Oct 2010 9th INTERNATIONAL CONFERENCE FOR SENIOR PATENT ADMINISTRATORS IP
14 Oct 2010 THE ROLE OF THE RESPONSIBLE PERSON GxP
21 Oct 2010 OPPOSITIONS AND APPEALS ~ THE EPO CASE LAW IP
22 Oct 2010 PATENTS ~ THE EPO CASE LAW IP
09 Nov 2010 DRAFTING AND NEGOTIATING CLINICAL TRIALS AGREEMENTS Legal
25 Nov 2010 EQE PAPER D REVISION COURSE IP
ASTHMA / ALLERGIC RHINITIS Pharmaceutical
PHARMACEUTICAL ORIGINATION AND ARTWORK 2010 GxP
OPHTHALMIC DRUG DELIVERY Medical Devices
CLINICAL TRIALS IN INDIA Pharmaceutical
PHARMACODYNAMICS Pharmaceutical
THE PATENT TREATIES OF EUROPE IP
ONLINE EXAM - CERTIFICATE IN GCP & EU CLINICAL TRIAL DIRECTIVE Pharmaceutical
INTERMEDIATE VETERINARY STATISTICS Animal Health
DISTRIBUTION OF MEDICINES - FROM GOOD PRACTICE TO BEST PRACTICE: GxP
An Introduction to VETERINARY STATISTICS Animal Health
REIMBURSEMENT FOR MEDICAL DEVICES Medical Devices
FDA COMBINATION PRODUCTS Medical Devices
FDA APPROVAL PROCESS FOR MEDICAL DEVICES Medical Devices
IP DUE DILIGENCE IP
FREEDOM TO OPERATE IP
ADVANCED THERAPIES REGULATION Pharmaceutical