A ProPharma Group knowledge center & resource

+1 (847) 295-7160

View Cart Log In

View Cart

« All Courses

Computer System Validation (CSV) for Cloud/COTS – EU – September 2025

September 22, 2025 @ 10:30 am - September 24, 2025 @ 4:00 pm CEST

$1,599.00 – $3,198.00

Learn to Validate for Your Cloud-based, SaaS, COTS, or OOTB Application

This class has been designed to ensure that you leave knowing what to validate, how to validate, and when to leverage vendor-supplied documentation in your validation. You will also learn the necessity and power of vendor assessments and risk-based validation.

Time: 10:30 AM – 4:00 PM Central European Time each day (8:30-2:00 PM PT / 11:30-5:00 PM ET) Not your time zone? Try this converter tool.

Read more about this course

Tickets

The numbers below include tickets for this event already in your cart. Clicking "Get Tickets" will allow you to edit any existing attendee information as well as change ticket quantities.
Single Seat
$ 1,599.00
Unlimited
Buy 2, Get 1 Free
$ 3,198.00
Unlimited
Quantity: 0
Total: $ 0.00

Details

Start:
September 22, 2025 @ 10:30 am CEST
End:
September 24, 2025 @ 4:00 pm CEST
Cost:
$1,599.00 – $3,198.00
Event Category:

Venue

Online

Other

Course Number
CS200
Professional Development Credits
16 hours / PDUs
Continuing Education Units
1.6

Related Courses

Search the Library

Find and download the latest FDA Warning Letters, Regulations, Guidelines, Templates, and SOPs.

Everything Validation

Validation Center

Validation Center brings you all the resources needed for computer system validation. We provide one-stop access to validation experts, training, and tools.

propharma logo

About ProPharma

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization), ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile drug and device programs. For more information, please visit www.propharmagroup.com.
US & Canada | UK | Europe | APAC
800 Hillgrove Avenue, Suite 201 Western Springs, IL 60558 | +1 (847) 295-7160

Company


Stay Connected

Be the first to know about upcoming classes and free webinars.


© 2024 ProPharma Group | Privacy Policy | Terms