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Management Forum - 2024, 2025, 2026 (page 2)
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"Management Forum" Events
(p. 2)
Showing 101 - 200 conferences out of 226
Effective Defence of EPO Patent Applications
18 Jul 2025
Online Event
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report
21-22 Jul 2025
Online Event
Stability Testing of Pharmaceuticals and Biopharmaceuticals
21-22 Jul 2025
Online Event
FDA Approval Process for Medical Devices
22-23 Jul 2025
Online Event
An Introduction to the Design and Development of Medical Devices
23-24 Jul 2025
Online Event
Medical Device Regulation in the Eurasion Union, Russia and the CIS
23-24 Jul 2025
Online Event
An Essential Overview of Pharmacovigilance
08-09 Sep 2025
Online Event
Navigating EU (European Union) and FDA (Food and Drug Administration) Regulations for Drug/Device and Device/Drug Combination Products
10-11 Sep 2025
Online Event
Business and Contract Law
15-16 Sep 2025
London, United Kingdom
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting
15-16 Sep 2025
Online Event
Human Factors and Usability Engineering in the Development of Drug Delivery Products
16-17 Sep 2025
London, United Kingdom
Strategic IP (Intellectual Property) Planning
17-19 Sep 2025
Online Event
Clinical Quality Management Systems
18-19 Sep 2025
Online Event
Process Validation with Qualification
20-22 Sep 2025
London, United Kingdom
An Essential Overview of the Pharmaceutical and Biotech Industries
22 Sep 2025
Online Event
Regulatory Affairs for Support Staff
22-23 Sep 2025
Online Event
Effective Defence of EPO Patent Applications
22 Sep 2025
Online Event
Advanced Drafting Techniques for Successful EPO Patent Applications
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
Successful Medical Writing – from Protocol to CTD
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
Reviewing and Negotiating Technology Transfer and Licensing Agreements
02-03 Oct 2025
Online Event
Development of Combination Products: Critical Interactions
02-03 Oct 2025
Online Event
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union
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
Metered Dose Inhaler (MDI) Technology
08-09 Oct 2025
Online Event
Pharmaceutical Regulatory Affairs in Asia
08-10 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
IP Due Diligence & Freedom-to-Operate in Practice
04-05 Nov 2025
Online Event
Introduction to the In-Vitro Diagnostic Regulation (IVDR)
04-05 Nov 2025
Online Event
Introduction to Veterinary Pharmacovigilance
05-06 Nov 2025
Online Event
The Pharma Mini MBA
05-07 Nov 2025
Online Event
An Essential Overview of the Medical Device Industry
07 Nov 2025
Online Event
Biotechnology for the Non-Biotechnologist
10-14 Nov 2025
Online Event
Business and Contract Law
10-11 Nov 2025
Online Event
Positive Persuading and Influencing Skills for Pharma Professionals
10-11 Nov 2025
Online Event
Medical Device Studies: Clinical Evidence
10-11 Nov 2025
Online Event
Stability Testing of Pharmaceuticals and Biopharmaceuticals
10-11 Nov 2025
Online Event
Agile Leadership for Pharma and Biopharma Professionals in a hybrid world
17-18 Nov 2025
Online Event
Managing Risks as a Corporate In-house Lawyer
17 Nov 2025
Online Event
Signal Detection and Regulatory Expectations
18-21 Nov 2025
Online Event
Formal Requirements of the European Patent System
18-21 Nov 2025
Online Event
GCP (Good Clinical Practice) and Clinical Research Update - Hot Inspection Topics
21 Nov 2025
Online Event
The Common Technical Document
24-25 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
FDA Approval Process for Medical Devices
02-03 Dec 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
CAPA (Corrective and Preventative Action)
Apr 2025
Online Event
Medical Device Regulations in the Middle East and North Africa
Jun 2025
Online Event
Patent Protection for Software-Related Inventions in Europe and the USA
Sep 2025
Successful Medical Writing – from Protocol to CTD
2025
The Medical Device Summer School - From Concept to CE Marking
Dec 2025
A Regulatory Update on Animal Feed and Feed Additives in the EU, USA and China
Dec 2025
An Introduction to Pharmaceutical Packaging
Jan 2026
An Essential Overview of the Pharmaceutical and Biotech Industries
Jan 2026
Online Event
Regulatory Affairs for Support Staff
Jan 2026
Clinical Quality Management Systems
Jan 2026
Online Event
An Essential Overview of Pharmacovigilance
Jan 2026
Online Event
Process Validation with Qualification
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
Medical Device Studies: Regulatory Requirements and Adverse Event Reporting
Jan 2026
Online Event
Pharmacovigilance QMS & Inspection Preparation
Jan 2026
Online Event
A Practical Guide to Producing and Maintaining the PSMF
2026
Reviewing and Negotiating Technology Transfer and Licensing Agreements
Feb 2026
Online Event
An Introduction to the Medical Device Regulation
2026
Pharmaceutical Regulatory Affairs in the Middle East
2026
Online Event
The Patent Administrator
Feb 2026
Metered Dose Inhaler (MDI) Technology
Feb 2026
Online Event
Business and Contract Law
Feb 2026
Effective Technical Writing and Editing
Feb 2026
Online Event
Clinical Overview and Clinical Summary: Creating Effective Marketing Authorisation Application
Feb 2026
Online Event
Formal Requirements of the European Patent System
2026
Managing Vendor/CRO (Contract Research Organisation)/CMO (Contract Manufacturing Organisation) Oversight
2026
Online Event
The FDA (Food and Drug Administration) Drug Approval Process
Feb 2026
Online Event
Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations
2026
Variations to Marketing Authorisations
Feb 2026
Pharmaceutical Development of ATMPs
Feb 2026
Online Event
Development of Combination Products: Critical Interactions
Feb 2026
Online Event
Stability Testing of Pharmaceuticals and Biopharmaceuticals
2026
Online Event
Pharmaceutical Regulatory Affairs in Asia
Feb 2026
Online Event
Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union
Feb 2026
Online Event
Clinical Evaluation of Medical Devices: The Clinical Evaluation Report
2026
Managing Risks as a Corporate In-house Lawyer
Mar 2026
Online Event
Signal Detection and Regulatory Expectations
Mar 2026
Online Event
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