QAS Plus

Quality Assurance Services Plus

QAS Plus

QAS+ Information Portal

QAS+ has developed a new QAS+ Information Portal for Pharmaceutical and related Industries with the collaboration of worldwide professionals. Information in the fields of regulations, directives, guidelines, procedures, processes, advice, training are available about manufacturing, laboratory, clinical, pharmacovigilance & safety, regulatory affairs, medical affairs, etc.

In conjunction to the QAS+ Information Portal, registered members can visit the QAS+ IP Forum for commenting articles, giving advice and requesting specific information to other members.

Both QAS+ Information Portal and QAS+ IP Forum require their specific registration for normal use.

More about QAS+ IP

All documents in the QAS+ Information Portal are downloaded directly from the websites of Competent Authorities and other related entities. For a real experience, you must register into the website and collate your professional information at no cost, with just your small contribution.

When registering at QAS+ Information Portal, you receive 5 credit units and you can add more credit by submitting new articles. To facilitate your learning how to submit articles, visit QAS+ Demo Information Portal.

All links are under the QAS+ Information Portal menu

Tools

QAS+ has elaborated several techniques available on QAS+ Information Portal , such as an Excel spreadsheet to review and analyze GxP audit findings, an Excel program to conduct standardised GxP process audits and an interactive ICH GCP guidelines model.

For more information, visit the Techniques link (registration required for downloading some documents), or contact This e-mail address is being protected from spambots. You need JavaScript enabled to view it .

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