Viseven

SEPTEMBER 6, 2024

All of it is done to assure data integrity—the glue that holds together all measures and actions performed to keep the data safe, error-free, and complete. In our new article, you will learn more about data integrity in the pharmaceutical and life sciences industry and why maintaining it matters so much.

Health and Personal Care Stores 52

Health and Personal Care Stores Documentation Data Entry Communication 52

GMPSOP

APRIL 19, 2024

We had to ensure that those Excel spreadsheets were processing GMP data accurately and reproducibly so that our decision did not adversely affect the patient’s health. Excel spreadsheets are widely used in pharmaceutical operations, from simple data entry in the registers to complex data processing using functions and formulas.

Documentation 52

Documentation Data Entry Communication Pharmaceutical Companies 52

GMPSOP

JUNE 28, 2024

This article will explore more elements of unplanned deviations than planned deviations. incorrect data entry). This article mainly explored the management practices of unplanned deviation and the investigational approach to unplanned deviations. It is likely to be caused by human error or another isolated event.

Documentation 59

Documentation Packaging Labelling Pharmaceutical Manufacturing 59

GMPSOP

OCTOBER 28, 2023

. – Record or capture all generated raw data directly, promptly, and legibly. – Use traceable data sheets or sequentially numbered notebooks. – Date and sign or initial data entries on the day of entry. – Archive records so that they are protected, secured, and easily retrievable.

Documentation 52

Documentation Method Validation Packaging Data Entry 52

GMPSOP

DECEMBER 24, 2023

This article will focus on G(C)LP due to its significance in everyday laboratory operations. – Record or capture all generated raw data directly, promptly and legibly. – Use traceable data sheets or sequentially numbered notebooks. – Date and sign or initial data entries on the day of entry.

Documentation 40

Documentation Method Validation Packaging Data Entry 40

Pharmaceutical Technology

SEPTEMBER 7, 2022

The process of actioning case reports is typically split into six stages: case receipt, triage (deciding whether a case should be classified as serious, non-serious or a non-event), data entry, quality review, medical review, and submission. Redesigning the translation process to increase efficiency.

Data Entry 52

Data Entry Vaccines Documentation Labelling 52

GMPSOP

JULY 31, 2023

In this article, we will explore what operational qualification entails, its importance, and FDA requirements. The data entry and retrieval process, user access and security, electronic signature, audit trail, system integration, performance, printing, etc. Also, it can be integrated with other external interfaces.

Documentation 52

Documentation Dosage Labelling Data Entry 52

pharmaphorum

OCTOBER 4, 2022

In this article, Ben Hargreaves takes a look at the renewed effort to tackle deaths from cancer in the US through the Cancer Moonshot. Central to the initiative is the aim to gather data from willing participants that can provide greater insights into cancer development and treatment over time.

Documentation 105

Documentation Data Entry HIPAA 105