pharmaphorum

OCTOBER 20, 2022

Apart from manual transfers of documents between colleagues, the data is relegated to one’s hard drive and can’t be queried at scale to evaluate performance or to inform future projects. How can we take an innovative approach to drive commercial success across the pharmaceutical industry?

Pharmaceutical Companies 89

Pharmaceutical Companies Pharmaceutical Companies Data Entry Documentation 89

pharmaphorum

SEPTEMBER 11, 2020

Indeed, handling such data and finding resources to clean and manage it was overwhelmingly cited by Pharma Intelligence respondents as the most urgent challenge facing researchers over the next five years. Clearing redundant data then becomes difficult, and programming complex edit checks becomes impossible.

Data Entry 72

Data Entry Documentation 72

Pharmaceutical Technology

JUNE 15, 2023

As clinical trials generate a massive amount of data, it can be challenging for researchers to manually review all of this data to uncover meaningful insights. For example, important information may be locked in knowledge silos or gained through experience, making it difficult to find or document.

Compounding 52

Compounding Adverse Reactions Dosage Documentation 52

ISPE

JUNE 21, 2023

The ISPE Sub-Committee for Paperless Validation has defined ‘Paperless Validation Systems’ as Paperless solutions enable validation lifecycle deliverables to be generated, approved, and more importantly, testing to be completed without the need for the printing of paper test documents. If It Is Not Documented, It Did Not Happen.

Documentation 52

Documentation Data Entry Compounding FDA 52

pharmaphorum

OCTOBER 4, 2022

It also enhances the patient experience with easy-to-understand clinical trial information, such as a video about the Biobank study, as well as informed consent documents for electronic signature,” he continued. Facilitating patient understanding and consent. Informed consent is crucial to recruiting the patient to the study.

Documentation 94

Documentation Data Entry HIPAA Insurance 94

pharmaphorum

OCTOBER 6, 2020

To improve data confidence regulatory executives should take a four-step approach to change how they: Collect Data: Life sciences organisations should utilise cloud-based solutions with global access that facilitates one repository with a single source of truth and eliminates the use of local file sharing and servers.

Documentation 93

Documentation Communication Labelling Data Entry 93

pharmaphorum

SEPTEMBER 6, 2021

Many practitioners have expressed the feeling that EHRs cause far too much of their time ultimately being spent on data entry. Additionally, issues such as poor quality documentation due to template-based reporting, and incompatibilities between different systems have further caused headaches and increased inefficiencies.

Medical Records 138

Medical Records Health and Personal Care Stores Data Entry Hospitals 138

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.

Data Entry 52

Data Entry Vaccines Documentation Labelling 52

ISPE

MAY 11, 2023

The key to data integrity compliance is a well-functioning data governance system 1 , 2 in which the data flow path for all business processes and equipment—such as in manufacturing, laboratory, and clinical studies—is fully understood and documented by a detailed process data flow map.

Packaging 52

Packaging Documentation Communication Data Entry 52

pharmaphorum

DECEMBER 6, 2022

In most cases, the EHRs and EDCs don’t communicate, so in order to share that data with trial organisers, staff members at medical centres must manually copy data between the EHR and an EDC. Peleg expects that in the next five years, EHR to EDC linkage and data streaming will be the gold standard for clinical trials.

Data Entry 98

Data Entry Communication Hospitals Documentation 98