-

UK Navigating Term and Termination Clauses in Commercial Contracts Training Course (ONLINE EVENT: June 24, 2025) - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Navigating Term and Termination Clauses in Commercial Contracts Training Course" training has been added to ResearchAndMarkets.com's offering.

Understanding the intricacies of term and termination clauses is crucial for ensuring the longevity and stability of business and commercial agreements. This course provides you with the tools to manage contract lifecycles and handle terminations smoothly and legally.

This information packed session will give you an invaluable opportunity to ask the expert trainer about any particular issues affecting your business and gain tips and insights from his vast experience.

Benefits of attending

  • Understand the reasons for termination and what constitutes breach
  • Gain insights into drafting clear and enforceable term and termination clauses
  • Learn techniques to handle contract renewals, extensions and terminations
  • Explore the implications of termination and the Corporate Insolvency and Governance Act 2020
  • Get to grips with the consequences of termination

Who Should Attend:

  • In-house counsel
  • Private practice lawyers
  • Contract managers
  • Business executives
  • Contract administrators
  • Procurement professionals
  • Project managers
  • Legal professionals and advisors

Key Topics Covered:

Termination clauses

Term

Expiry

Reasons for termination

Background law default

Breach:

  • Material breach
  • Persistent breach
  • Any breach

Insolvency

Termination and Corporate Insolvency and Governance Act 2020

Change of control

Pointers and collection

Consequences of termination

For more information about this training visit https://www.researchandmarkets.com/r/dqasfd

About ResearchAndMarkets.com

ResearchAndMarkets.com is the world's leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends.

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./ CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

Industry:

Research and Markets

Release Versions
English

Contacts

ResearchAndMarkets.com
Laura Wood, Senior Press Manager
press@researchandmarkets.com
For E.S.T Office Hours Call 1-917-300-0470
For U.S./ CAN Toll Free Call 1-800-526-8630
For GMT Office Hours Call +353-1-416-8900

More News From Research and Markets

Computer System Validation (CSV) Training Course: Regulations Impacting Your Systems and Hands-on Practice Writing Validation Documents (Jan 27th - Jan 29th, 2026 & On-Demand) - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Computer System Validation (CSV) Training Course (Jan 27th - Jan 29th, 2026)" training has been added to ResearchAndMarkets.com's offering. A course designed to completely immerse you in computer system validation. This course delivers comprehension of the regulations impacting your systems and hands-on practice writing validation documents. You will leave ready to lead efficient, effective, inspection- ready validation projects. Registration Includes: Checklist of...

Understanding Medical Device Regulatory Pathways - 510(k), PMA & Exemptions Webinar - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Understanding Medical Device Regulatory Pathways - 510(k), PMA & Exemptions (January 15, 2026)" training has been added to ResearchAndMarkets.com's offering. This expert-led 3-hour webinar provides a comprehensive introduction to the key regulatory pathways for medical device submissions in the US market. The regulation and control of new or substantially changed medical devices for sale in the US is based on the 510(k), PMA or DeNovo submission process. This w...

Medical Devices: Section 522 of the Federal Food, Drug, and Cosmetic Act (FD&C Act) Course: Developing Effective Post Market Surveillance and Complaint Handling Systems Training - ResearchAndMarkets.com

DUBLIN--(BUSINESS WIRE)--The "Medical Devices: Developing Effective Post Market Surveillance and Complaint Handling Systems Course (Jan 22nd - Jan 23rd, 2026)" training has been added to ResearchAndMarkets.com's offering. What are U.S. FDA CGMP expectations/requirements for Post Market Surveillance and Complaint Handling? This seminar will examine Section 522 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), as well as appropriate articles / Annexes of the EU's MDR, which require manu...
Back to Newsroom