Legislative Updates – Continued Professional Education
Print
Keep up-to-date with the latest legislation
Dates:
Thursday 24 to Friday 25 July 2025
Venue:
NSF Health Sciences Boston Office, Boston, MA, USA
Cost:
$950.00
$760.00 (early bird booking discount)
Type: Pharmaceutical
About this course
Pharmaceutical legislation changes impacting both the supply of clinical and commercial drug product are reviewed in detail, including any significant legislation impacting manufacture, supply and distribution. Particular focus is given to legislation changes in Europe and in the USA. However, important changes by regulatory agencies including the CFDA, ANVISA, CDSCO (India) and other major bodies are reviewed. The implications of these changes are put into context to help you ensure your company is compliant with the most current requirements and expectations.
This legislative update is the cornerstone seminar offered in Europe for our Qualified Persons and in the USA for graduates of our Quality Leadership Program. It will benefit industry professionals in Quality, Regulatory, Manufacturing and other technical disciplines. It is designed to be current, relevant, and delivered in an interactive and enjoyable format.
Sign up early to reserve space as this is a popular course!
Course outline
Topics are adjusted prior to the preparation of this course to ensure the latest changes are covered. Topics which are covered fall within the following major headings:
- Legislation impacting the global supply chain
- FDA Safety and Innovation Act implementation status and what companies are doing in preparation
- European Falsified Medicine Directive
- Legislation Impacting Pharmaceutical Manufacturing Operations including Development
- EudraLex Annex updates
- Process validation guidance
- Guidelines impacting contract manufacturing
Venue
NSF Health Sciences Boston Office, Boston, MA, USA
These courses will take place in the
The Washington Marriott
1221 22nd St NW
Phone: (202) 872-1500
Washington, District of Columbia 20037
United States
Tutors
We believe that our team of experts are the best available. Not only have they got years of experience in the industry, but they are committed to tutoring and helping those inside the industry to improve and raise the standards. We understand that you attend courses to learn about the latest regulations and to get your questions answered.
Our experts for this course are:
What you've said
“This was great for fulfilling my annual GMP training.”
Lana Lyday, CSL Behring, USA
“Before this class I only had minimum knowledge of this subject. I have learned so much from this course that will assist me in my career!”
Jerry Amado, Drug Development Resources, USA
An NSF International Company 
