article thumbnail

Leveraging Technology | Case Study

PharmaState Academy

You foster an environment of open communication and collaboration, where every voice is heard and valued. Option 02 Increasing paperwork and manual data entry. You challenge the team to think creatively and strategically about how to navigate the upcoming months, encouraging them to share ideas and insights.

article thumbnail

Considerations for safety data migration methods

European Pharmaceutical Review

Pharmaceutical companies regularly transfer databases as they shift to new systems or change service providers in pursuit of higher quality and increased efficiency. There is a high degree of focus on the verification and validation activities performed to ensure that data integrity is maintained throughout all steps of the project.

Insiders

Sign Up for our Newsletter

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.

article thumbnail

How using AI in clinical trials accelerates drug development

Pharmaceutical Technology

But before pharmaceutical companies can go to market with a breakthrough drug, they need to ensure safety and efficacy through clinical trials. Here are some ways companies are using AI in clinical trials. The need for new medical treatments and drugs has never been greater.

article thumbnail

RFID: The future of smart labelling?

Pharmaceutical Technology

Fresenius Kabi is a global healthcare company specialising in medicines and technologies for infusion, transfusion and clinical nutrition. In August of 2022, Fresenius Kabi announced a three-year plan to add GS1 Data Matrix barcodes, also known as 2D barcodes, to its US pharmaceutical portfolio.

Labelling 105
article thumbnail

Guideline for Excel spreadsheet validation

GMPSOP

Excel spreadsheets are widely used in pharmaceutical operations, from simple data entry in the registers to complex data processing using functions and formulas. When data is received through an electronic interface, the report must identify the instrument system or software program that communicated the data.

article thumbnail

How to perform operational qualification – step by step

GMPSOP

The data entry and retrieval process, user access and security, electronic signature, audit trail, system integration, performance, printing, etc. The FDA sets stringent requirements for operational qualification for critical equipment and systems to ensure the safety and efficacy of pharmaceutical products.