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Conferences in The Rembrandt Hotel (past events)
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Conferences in The Rembrandt Hotel
London, UK
(past events)
Showing 201 conferences
FDA Approval Process for Medical Devices
Sep 2024
The Patent Administrator
Aug 2024
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report
Aug 2024
An Introduction to the Medical Device Regulation
Aug 2024
Successful Medical Writing
Jul 2024
Drafting Commercial Contracts for the Pharmaceutical Industry
Jul 2024
Global Conference on Gynecology, Obstetrics and Womens Healthcare
Jun 2024
World Congress on Biopolymers and Biomaterials
Nov 2022
Developing High Performance HR Business Partner and Consulting Skills
May 2022
Biological Evaluation of Medical Devices
Feb 2022
Advanced PCT Formalities
Nov 2021
EU Clinical Trial Regulation: Overview and Implementation
Apr 2021
Effective Contract Management
Nov 2020
The Art of European Claim Drafting
Nov 2020
New Medical Device Regulation
Oct 2020
Pharmacovigilance Aspects of Licensing Agreements
Oct 2020
Intellectual Property for Pharma Regulatory Affairs
May 2020
The Role and Skills of a Valuable HR Assistant
Apr 2020
Effective Technology Transfer
Apr 2020
EU Pharmaceutical Regulations & Strategy
Apr 2020
Biosimilars
Apr 2020
Risk Management in Clinical Research
Mar 2020
Pharmaceutical Regulatory Affairs in Africa
Mar 2020
Injectable Drug Delivery
Mar 2020
Registration of Veterinary Vaccines in the USA and Canada
Mar 2020
A Practical Approach to Veterinary Vaccine Development and Registration in the EU
Mar 2020
Effective Delegation Skills
Mar 2020
EPO Oppositions and Appeals - the Case Law and Workshop
Mar 2020
Connectivity in Medical Technology
Feb 2020
How to Improve Accuracy and Attention to Detail
Feb 2020
Medical Device Regulations in Latin America
Feb 2020
Effective Training Skills and Processes in the Pharma Industry
Feb 2020
Decision Making & Problem Solving in the Pharma Industry
Feb 2020
Clinical Trial Regulatory Requirements
Jan 2020
A Practical Guide to Writing Risk Management Plans (RMPS)
Jan 2020
Impact of Brexit on the Pharma & Medical Device Industries
Dec 2019
Advanced Veterinary Pharmacovigilance
Dec 2019
The New EU Animal Health Legislation for Veterinary Medicinal Products
Dec 2019
Borderlines Between Medicines and Food
Dec 2019
US Patent Practice
Dec 2019
Pharmacovigilance
Dec 2019
How to Write Effective SOPs
Dec 2019
Leading & Developing Successful Pharma Teams
Nov 2019
Drafting and Negotiating International Agency and Distribution Agreements
Nov 2019
Inhaled Drug Delivery
Nov 2019
Effectively Managing Legal Risk and Preserving Reputation
Nov 2019
Dealing with Difficult People
Nov 2019
Presentation Skills Masterclass
Oct 2019
Drafting Commercial Contracts
Oct 2019
Pharmaceutical Packaging, Labelling and Artwork Origination
Oct 2019
Pharmacovigilance
Jun 2019
Dry Powder Inhalers: Annual Conference
Jun 2019
Mindfulness in the Workplace
May 2019
Powerful Negotiation Skills
May 2019
Exploring Routes to Market for Herbals
May 2019
Working with Emotional Intelligence
Apr 2019
The New ICH GCP E6 R2 Addendum
Apr 2019
Powerful Communication & Presentation Skills
Mar 2019
The New ICH GCP E6 R2 Guideline
Feb 2019
Development of Drug/Device and Device/Drug Combination Products
Nov 2018
Conflict Management
Oct 2018
Wearable Drug Delivery
Oct 2018
Pharmacoepidemiology
Jun 2018
Assertiveness for Maximum Impact
Jun 2018
Stress and Time Management
May 2018
An Essential Overview of Medical Information
Apr 2018
Emotional Intelligence - Enhancing your Personal Impact
Apr 2018
Basic Principles of Pharmacokinetics
Mar 2018
Building High Performance Teams
Dec 2017
Improving Processes and CAPA
Dec 2017
Abridged Applications
Nov 2017
Pharmaceutical Regulatory Affairs in Latin America
Nov 2017
Drafting and Managing Pharmaceutical Safety Exchange Agreements
Nov 2017
Planning, Forecasting and Budgeting
Nov 2017
Conflict Management
Oct 2017
ISO 13485: Quality Management System for Medical Devices
Sep 2017
Latest Developments in Pharmacovigilance
Jul 2017
Drafting and Negotiating International Commercial Contracts
May 2017
Introduction to the Medical Device Directives
May 2017
Keeping Up-To-Date as a (GMP) Qualified Person
Mar 2017
DSURS and PBRERS
Jan 2017
The Borderline Between Medicines and Foods
Dec 2016
Comprehensive Practical Review of the EU Pharmacovigilance Modules
Nov 2016
Conflict Management
Oct 2016
Improving Performance Through Increased Accuracy and Attention to Detail
Sep 2016
Pharmacovigilance for Support Staff
Jun 2016
Clinical Trial Regulatory Guideline Requirements
Jun 2016
Communication Alchemy
Mar 2016
New EU Pharmacovigilance Legislation
Nov 2015
An Introduction to the Medical Devices Directive
Nov 2015
Medical Device Regulation in Asia/Pacific Markets
Sep 2015
Leadership Skills
Jul 2015
Keeping Up To Date as a Qualified Person Refresher and Intermediate Training
Jul 2015
Pharmaceutical Registration Strategies in Europe & the US for Generics & Super Generics
Jul 2015
QPPV Workshop
Jul 2015
Clinical Trial Guidelines & the New Clinical Trial Regulation
Jun 2015
Capsule Based Inhalers: Understanding the Science
Jun 2015
An Introduction to Medical Device Software: Regulations & Requirements
May 2015
Clinical Trial Transparency
Apr 2015
An Essential Guide to Medical Information
Apr 2015
A Practical Approach to Pharmacovigilance
Apr 2015
Introduction to the Crop Protection Industry in the EU
Mar 2015
Publications Planning – Updates and Developments
Mar 2015
Handling Complex Commercial and Contract Negotiations
Feb 2015
Keeping up to Date as a Qualified Person
Feb 2015
The Cosmetics Regulation (EC) 1223/2009
Feb 2015
FDA Quality System Management for Medical Devices
Feb 2015
Novel Approaches to the Treatment of Cancer
Feb 2015
Cross-Cultural Leadership
Dec 2014
Change Management Skills for Pharmaceutical Professionals
Dec 2014
In Vitro Diagnostic Directive (IVDD)
Nov 2014
Update to Clinical Trial and Post Marketing Safety in the EU
Nov 2014
ISO 13485 for Medical Devices
Nov 2014
European CME Forum - Annual meeting
Nov 2014
Combination Products in the EU
Nov 2014
Routine Duties of the Responsible Person
Oct 2014
Quality Management System for Practical Wholesalers
Sep 2014
Warehousing of Pharmaceuticals and Best Practices for Warehouse Temperature Mapping
Jun 2014
Transportation of Pharmaceuticals and Best Practices for Transport Temperature Mapping
Jun 2014
Pharmaceutical Regulatory Requirements in Japan
Jun 2014
How to Edit Scientific, Medical and Technical Texts - Practical Workshop
Jun 2014
Understanding the Pharmaceutical Industry
Jun 2014
FDA GMP Requirements For Medical Devices - The Quality Management System
May 2014
Devils Advocate Auditor - An Overview of the Strategic Planning Process
Apr 2014
MEDICAL DEVICE CLINICAL STUDIES - Understand How to Conduct Pre and Post Market Medical Device Clinical Studies
Apr 2014
The Summary Of Product Characteristics
Mar 2014
An Essential Guide to Continuing Medical Education
Mar 2014
Distribution of Medicines - The New EU Good Distribution Practice Guide...Are You Prepared?
Mar 2014
Process Validation for Pharmaceuticals & Medical Devices in The EU & USA - Including Practical Workshop Exercises
Oct 2012
PS 9000-2011 in the Pharmaceutical Supply Chain - Standards for Pharmaceutical Packaging Materials and Components: New Requirements and Implications
Oct 2012
Optimising EU Reimbursement For Medical Devices - How to Build Value and Drive Reimbursement In The UK, Germany and France
Sep 2012
Understanding the Decentralised and Mutual Recognition Procedures
Sep 2012
Medical Device Regulations in Europe
Sep 2012
Introduction to Manuscript Writing - Two Day Intensive Course
Sep 2012
Impact of the New Pharmacovigilance Legislation - Key Industry and Regulatory Perspective
Sep 2012
FINANCIAL AWARENESS FOR INTELLECTUAL PROPERTY PROFESSIONALS
Jan 2012
EUROPEAN PATENTS - THE CASE LAW
Jan 2012
FDA MEDICAL DEVICE INSPECTIONS - Are You Prepared?
Dec 2011
THE PRACTICE OF ORAL PROCEEDINGS AT THE EUROPEAN PATENT OFFICE
Dec 2011
THE NEW ISO 14155 REQUIREMENTS FOR MEDICAL DEVICE CLINICAL STUDIES
Dec 2011
THE DEVELOPMENT SAFETY UPDATE REPORT (DSUR)
Nov 2011
FROM CORE SAFETY INFORMATION TO LOCAL LABELLING
Nov 2011
STABILITY TESTING
Nov 2011
ESSENTIAL GUIDE TO PUBLICATIONS PLANNING - Two Day Course
Nov 2011
PHARMACEUTICAL PACKAGING AND LABELLING
Nov 2011
THE BORDERLINE BETWEEN MEDICINES AND FOODS
Oct 2011
FDA ADVERSE EVENT REPORTING FOR PHARMACEUTICALS
Oct 2011
FDA GMP REQUIREMENTS FOR PHARMACEUTICALS
Oct 2011
SUCCESSFUL MEDICAL WRITING - Intensive Practical Course
Sep 2011
BIOTECHNOLOGY FOR NON BIOTECHNOLOGISTS - London
Sep 2011
REGULATORY AFFAIRS FOR SUPPORT STAFF ~ PART 2
Sep 2011
The Eu Cosmetics Directive And The New Cosmetics Regulations
Sep 2011
The EU Cosmetics Directive and the new Cosmetic Regulations
Sep 2011
Medical Device Regulations In Asia Pacific Market
Sep 2011
Corrective And Preventative Action (capa) And Process Improvement
Jul 2011
BASIC PCTFORMALITIES COURSE -For Administratorsand Legal Assistants
Apr 2011
Artwork Origination for Pharmaceutical Packaging
Mar 2011
ADVANCEDPHARMACOVIGILANCE
Mar 2011
BIO-SAFETY AND BIO-SECURITY
Mar 2011
DEVELOPING MEDICINES FOR COMPANION ANIMALS
Mar 2011
SCIENTIFIC ADVICE
Feb 2011
PERIODIC SAFETY UPDATE REPORTS (PSURs)
Feb 2011
SUPPLYING MEDICINES TO JAPAN
Feb 2011
SUCCESSFUL PATENT LITIGATION IN EUROPE AND THE U.S.
Feb 2011
WORKING THROUGH DRUG DEVELOPMENT - MANAGEMENT FORUM`S WINTER SCHOOL
Feb 2011
AN INTRODUCTION TO POST MARKETING SURVEILLANCE AND THE EUROPEAN MEDICALDEVICE VIGILANCE SYSTEM
Feb 2011
THE EFFECTIVE CRA / CLINICAL TRIAL ADMINISTRATOR / COORDINATOR
Jan 2011
ESSENTIAL OVERVIEW OF THE PHARMACEUTICAL INDUSTRY
Jan 2011
SUCCESSFUL IMPLEMENTATION OF MANUFACTURING SITE TRANSFERS
Jan 2011
Basic PCT Formalities Course
Apr 2010
Clinical And Post Marketing Safety
Apr 2010
Good Engineering Practice: (gep)
Apr 2010
AN OVERVIEW OF THE eCTD
Mar 2010
Claim And Specification Drafting For A Single Epo/uspto Patent Application
Mar 2010
Patent Infringement: Doctrines Of Equivalents And Purposive Construction In Us, Uk And Germany
Mar 2010
THE REGULATION OF rDNA TECHNOLOGY DERIVED DRUGS: BIOTECH SPECIFIC ASPECTS
Mar 2010
The Business Aspects Of Intellectual Property
Mar 2010
Fundamentals Of European Claim Drafting
Mar 2010
Case Law Of The Epo Boards Of Appeal For Mechanics / Electricity / Computer Software: Critical Issues
Feb 2010
Periodic Safety Update Reports
Feb 2010
International R&d Contracts, Collaborations And Joint Ventures
Feb 2010
Borderlines Between Cosmetics And Drugs
Feb 2010
Developing Medicines For Companion Animals - Management Forum`s Winter School
Feb 2010
Working Through Drug Development - Management Forum`s Winter School
Feb 2010
The Us Pharmaceutical Dossier
Feb 2010
Revision To The Medical Device Directives
Feb 2010
Fundamental Principles Of Patenting
Jan 2010
Advanced Publications Planning
Jan 2010
Introduction To Publication Planning And Strategy
Jan 2010
The effective CRA / Clinical Trial Administrator / Coordinator - How to be more proactive in your role
Jan 2010
COPD & Asthma
Jan 2010
IP As A Strategic Business Asset
Jan 2010
Introduction To Intellectual Property
Jan 2010
Active Comparator Studies
Jan 2010
CALIBRATION - The Risk Based Approach to Calibration Management
Jan 2010
Technology Licensing Masterclass
Jan 2010
Successful Patent Litigation In Europe
Dec 2009
How to Audit Regulatory Affairs & Clinical Trials
Dec 2009
US FDA Quality Systems & Medical Device Requirements
Dec 2009
Recurring Questions In Biotechnology And Chemistry Case Law Of The Epo Boards Of Appeal
Dec 2009
Document Management & Archiving
Dec 2009
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The Rembrandt Hotel Conferences 2025
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