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Visit our services section where we have computer validation document templates for amazing prices?

Wait for our online Computer Validation College that will make its debut in the coming months.

Our site is expanding, sign up below and we'll let you know our latest news.

Compval.com is dedicated to the fast paced world of Computer Validation in the pharmaceutical, medical device and biotechnology industries. Within Compval.com you should be able to find anything you ever wanted to know about Computer Validation.

So if it is a job in Computer Validation you are after, then be our guest and browse the available jobs and resumes. If you consider your career has been on hold long enough, then please register and upload your CV/Resume. Employers this service is currently free, so have a look around for that next prospective employee.

If you are just after information about what to do to validate a particular type of system, then why don't you visit our forum section and ask one of our resident industry experts the question. They would love to help.

If you're after training then you may like to visit our training section for news about training in Computer Validation. Shortly we will be supplementing this service with our very own Computer Validation College. Register now if you are interested in hearing more.

 

Compval.com is a professional consultancy company specializing in Computer Validation for the pharmaceutical, medical device and biotechnology industries.
We operate from a network of offices throughout the world. We currently have regional offices in the US, Europe and Asia.
We have worked for a wide range of Pharmaceutical companies and with a wide range of industry equipment.

 

Compval.com is able to meet all your Computer Validation needs.
Our services include:

• Identifying the most appropriate validation and test strategy to match you application and business needs.

• Developing and preparing policy, plan and procedure documents to meet the appropriate strategy.

• Developing and preparing pre-qualification and qualification documentation

• Performing Vendor/Supplier audits.

• Developing and executing of test protocols.

• Performing QA activities to oversee supplier software development.

• Conducting Gap Analysis studies of existing Computer Systems against current industry expectations.

• Perform pre-regulatory audit reviews

• Perform 21 CFR Part 11 assessments on computer system Developing and preparing pre-qualification and qualification documentation.In addition, Compval provides a range of training material that can be tailored for client needs. Our trainers are well versed with GAMP guidelines, EU, and FDA regulations with respect to computerised systems validation.

At Compval.com, our aim is to provide good value, practical advice and to seek a long-term relationship with our clients.