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Management Forum - 2024, 2025, 2026 (page 2)
"Management Forum" Events
(p. 2)
Showing 101 - 194 conferences out of 194
Regulatory Affairs for Support Staff
22-23 Sep 2025
Online Event
An Introduction to Pharmaceutical Packaging
24-26 Sep 2025
London, United Kingdom
Pharmacovigilance QMS & Inspection Preparation
25-26 Sep 2025
Online Event
Effective Technical Writing and Editing
01 Oct 2025
Online Event
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application
01-02 Oct 2025
Online Event
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union
02-03 Oct 2025
Online Event
Development of Combination Products: Critical Interactions
02-03 Oct 2025
Online Event
Advanced Pharmacovigilance
06-10 Oct 2025
Online Event
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations
07-10 Oct 2025
Online Event
The FDA (Food and Drug Administration) Drug Approval Process
07-08 Oct 2025
Online Event
Pharmaceutical Regulatory Affairs in Asia
08-10 Oct 2025
Online Event
Metered Dose Inhaler (MDI) Technology
08-09 Oct 2025
Online Event
Pharmaceutical Development of ATMPs
13-14 Oct 2025
Online Event
The Patent Administrator
13 Oct 2025
Online Event
Variations to Marketing Authorisations
15-16 Oct 2025
Online Event
Managing Vendor/CRO (Contract Research Organisation)/CMO (Contract Manufacturing Organisation) Oversight
16-17 Oct 2025
Online Event
Mastering Risk Management in the Patent Landscape - Freedom to Operate (FTO) Training Course
20 Oct 2025
Online Event
Pharmaceutical Regulatory Affairs in the Middle East
21-22 Oct 2025
Online Event
An Introduction to the Medical Device Regulation
03-05 Nov 2025
Online Event
Introduction to Veterinary Pharmacovigilance
05-06 Nov 2025
Online Event
The Pharma Mini MBA
05-07 Nov 2025
Online Event
Formal Requirements of the European Patent System
18-21 Nov 2025
Online Event
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report
25-26 Nov 2025
Online Event
Veterinary Pharmaceutical Submissions in the EU
25-26 Nov 2025
London, United Kingdom
Pharmaceutical Regulatory Affairs in China 2025
26-27 Nov 2025
Online Event
Medical Device Regulation in the Eurasion Union, Russia and the CIS
08-09 Dec 2025
Online Event
An Introduction to the Design and Development of Medical Devices
10-11 Dec 2025
Online Event
Data Integrity and Document Management
11 Dec 2025
Online Event
A Practical Guide to Producing and Maintaining the PSMF
03 Oct 2026
Medical Device Studies: Clinical Evidence
Mar 2025
Signal Detection and Regulatory Expectations
Mar 2025
Stability Testing of Pharmaceuticals and Biopharmaceuticals
Mar 2025
Successful Medical Writing – from Protocol to CTD
2025
FDA Approval Process for Medical Devices
Mar 2025
Positive Persuading and Influencing Skills for Pharma Professionals
Mar 2025
Online Event
Reviewing and Negotiating Technology Transfer and Licensing Agreements
Mar 2025
Online Event
Human Factors and Usability Engineering in the Development of Drug Delivery Products
Mar 2025
Agile Leadership for Pharma and Biopharma Professionals in a hybrid world
Mar 2025
Online Event
Introduction to the In-Vitro Diagnostic Regulation (IVDR)
Mar 2025
Managing Risks as a Corporate In-house Lawyer
Mar 2025
Online Event
An Essential Overview of the Medical Device Industry
Mar 2025
Online Event
Business and Contract Law
Mar 2025
GCP (Good Clinical Practice) and Clinical Research Update - Hot Inspection Topics
Mar 2025
Online Event
Advanced Drafting Techniques for Successful EPO Patent Applications
Mar 2025
IP Due Diligence & Freedom-to-Operate in Practice
Mar 2025
Effective Defence of EPO Patent Applications
Mar 2025
Strategic IP (Intellectual Property) Planning
Mar 2025
Online Event
The Common Technical Document
Mar 2025
CAPA (Corrective and Preventative Action)
Apr 2025
Online Event
Biotechnology for the Non-Biotechnologist
2025
Medical Device Regulations in the Middle East and North Africa
Jun 2025
Online Event
Introduction to the In-Vitro Diagnostic Regulation (IVDR)
Jul 2025
Successful Medical Writing – from Protocol to CTD
Jul 2025
Patent Protection for Software-Related Inventions in Europe and the USA
Sep 2025
A Regulatory Update on Animal Feed and Feed Additives in the EU, USA and China
Dec 2025
The Medical Device Summer School - From Concept to CE Marking
Dec 2025
An Essential Overview of the Pharmaceutical and Biotech Industries
Jan 2026
Online Event
Process Validation with Qualification
Jan 2026
Clinical Quality Management Systems
Jan 2026
Online Event
Regulatory Affairs for Support Staff
Jan 2026
Pharmacovigilance QMS & Inspection Preparation
Jan 2026
Online Event
An Essential Overview of Pharmacovigilance
Jan 2026
Online Event
A Practical Guide to Producing and Maintaining the PSMF
2026
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting
Jan 2026
Online Event
An Introduction to Pharmaceutical Packaging
Jan 2026
Mastering Risk Management in the Patent Landscape - Freedom to Operate (FTO) Training Course
Jan 2026
Online Event
Navigating EU (European Union) and FDA (Food and Drug Administration) Regulations for Drug/Device and Device/Drug Combination Products
Jan 2026
Online Event
Effective Technical Writing and Editing
Feb 2026
Online Event
An Introduction to the Medical Device Regulation
2026
Variations to Marketing Authorisations
Feb 2026
Development of Combination Products: Critical Interactions
Feb 2026
Online Event
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union
Feb 2026
Online Event
Pharmaceutical Regulatory Affairs in the Middle East
2026
Online Event
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report
2026
The FDA (Food and Drug Administration) Drug Approval Process
Feb 2026
Online Event
Pharmaceutical Development of ATMPs
Feb 2026
Online Event
Pharmaceutical Regulatory Affairs in Asia
Feb 2026
Online Event
Metered Dose Inhaler (MDI) Technology
Feb 2026
Online Event
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations
2026
Formal Requirements of the European Patent System
2026
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application
Feb 2026
Online Event
Managing Vendor/CRO (Contract Research Organisation)/CMO (Contract Manufacturing Organisation) Oversight
2026
Online Event
The Patent Administrator
Feb 2026
Introduction to Veterinary Pharmacovigilance
Mar 2026
Online Event
Pharmaceutical Regulatory Affairs in China 2026
Mar 2026
Online Event
Advanced Pharmacovigilance
Mar 2026
Veterinary Pharmaceutical Submissions in the EU
2026
The Pharma Mini MBA
2026
Online Event
Data Integrity and Document Management
Apr 2026
Online Event
An Introduction to the Design and Development of Medical Devices
Apr 2026
Online Event
Medical Device Regulation in the Eurasion Union, Russia and the CIS
Apr 2026
Online Event
Regulatory Affairs for Support Staff
May 2026
Patent Protection for Software-Related Inventions in Europe and the USA
2026
An Introduction to the Medical Device Regulation
2026
Online Event
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