Management Forum
Government & Global Issues Conferences (p. 2)

Related topics
Showing 101 - 172 conferences out of 172

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 the In-Vitro Diagnostic Regulation (IVDR)

04-05 Nov 2025
Online Event

The Pharma Mini MBA

05-07 Nov 2025
Online Event

Introduction to Veterinary Pharmacovigilance

05-06 Nov 2025
Online Event

An Essential Overview of the Medical Device Industry

07 Nov 2025
Online Event

Business and Contract Law

10-11 Nov 2025
Online Event

Medical Device Studies: Clinical Evidence

10-11 Nov 2025
Online Event

Formal Requirements of the European Patent System

18-21 Nov 2025
Online Event

Signal Detection and Regulatory Expectations

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

Effective Defence of EPO Patent Applications

Mar 2025

The Common Technical Document

Mar 2025

Reviewing and Negotiating Technology Transfer and Licensing Agreements

Mar 2025
Online Event

FDA Approval Process for Medical Devices

Mar 2025

Managing Risks as a Corporate In-house Lawyer

Mar 2025
Online Event

Introduction to the In-Vitro Diagnostic Regulation (IVDR)

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

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

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

Pharmacovigilance QMS & Inspection Preparation

Jan 2026
Online Event

An Introduction to Pharmaceutical Packaging

Jan 2026

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

Mastering Risk Management in the Patent Landscape - Freedom to Operate (FTO) Training Course

Jan 2026
Online Event

Regulatory Affairs for Support Staff

Jan 2026

Pharmaceutical Regulatory Affairs in Russia and the Eurasian Union

Feb 2026
Online Event

Variations to Marketing Authorisations

Feb 2026

The FDA (Food and Drug Administration) Drug Approval Process

Feb 2026
Online Event

The Patent Administrator

Feb 2026

Pharmaceutical Regulatory Affairs in Asia

Feb 2026
Online Event

Pharmaceutical Development of ATMPs

Feb 2026
Online Event

Pharmaceutical Regulatory Affairs in the Middle East

2026
Online Event

Business and Contract Law

Feb 2026

Development of Combination Products: Critical Interactions

Feb 2026
Online Event

Clinical Evaluation of Medical Devices: The Clinical Evaluation Report

2026

Formal Requirements of the European Patent System

2026

Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations

2026

An Introduction to the Medical Device Regulation

2026

Managing Vendor/CRO (Contract Research Organisation)/CMO (Contract Manufacturing Organisation) Oversight

2026
Online Event

Effective Technical Writing and Editing

Feb 2026
Online Event

An Essential Overview of the Medical Device Industry

Mar 2026
Online Event

Introduction to the In-Vitro Diagnostic Regulation (IVDR)

Mar 2026

Veterinary Pharmaceutical Submissions in the EU

2026

Advanced Pharmacovigilance

Mar 2026

Introduction to Veterinary Pharmacovigilance

Mar 2026
Online Event

Signal Detection and Regulatory Expectations

Mar 2026
Online Event

Strategic IP (Intellectual Property) Planning

Mar 2026
Online Event

Medical Device Studies: Clinical Evidence

Mar 2026
Online Event

Pharmaceutical Regulatory Affairs in China 2026

Mar 2026
Online Event

The Pharma Mini MBA

2026
Online Event

Successful Medical Writing – from Protocol to CTD

Mar 2026

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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