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 98

Data Entry Documentation 98

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

Viseven

SEPTEMBER 6, 2024

Data integrity isn’t a software, service, or product; it encompasses various solutions contributing to improved data maintenance and quality. Importance of Data Integrity in the Pharma Industry It takes just one wrong data entry, breach, or incident for patients and clients to lose your trust.

Health and Personal Care Stores 52

Health and Personal Care Stores Documentation Data Entry Pharmaceutical Companies 52

European Pharmaceutical Review

MARCH 12, 2024

This can be achieved by implementing electronic systems with built-in controls to maintain data integrity, audit trails and access controls. Good documentation practices. Following good documentation practices (GDP) throughout all stages of data generation, collection, analysis and reporting is vital.

Documentation 98

Documentation Data Entry Communication Compounding 98

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 98

Pharmaceutical Companies Pharmaceutical Companies Data Entry Documentation 98

Viseven

DECEMBER 13, 2024

RPA employs software robots, or bots, to carry out tasks such as data entry and extraction, insurance claims processing, insurance verification, payroll calculations, document verification, employee onboarding, and many others. With healthcare RPA, it’s possible to mitigate errors and inaccuracies.

Data Entry 52

Data Entry Patient Care Insurance Hospitals 52

The Checkup by Singlecare

MARCH 16, 2023

Providing administrative support Pharmacy techs perform data entry tasks, such as entering prescriptions into a patient record and updating insurance information in pharmacy management systems, says Dr. Staiger. Instead, their roles will continue to evolve to include new responsibilities and skill sets, he says.

Data Entry 52

Data Entry Long-Term Care Facilities Insurance Immunization 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

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

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 Documentation Data Entry 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 105

Documentation Data Entry HIPAA Insurance 105