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Typical GMP documentation in a quality control laboratory

GMPSOP

In other word, you need GMP documentation specially developed and used for your laboratory to guide you through everything you do in the lab. Depending on the objective of the lab, the need for GMP documentation will change for the laboratory. The significance of well-designed GMP documentations is immense.

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How to implement good documentation practice in a GMP regulated plant

GMPSOP

Table of Contents Good documentation practice requires a system for control, implementation, maintenance and archival of GMP related documents and records. To implement good documentation practice and systems the site must assure that GMP documents and records are adequate, approved and in compliance with applicable GMP requirements.

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Data cleaning and harmonisation: A catalyst for innovation

Express Pharma

Data cleaning, the critical first step? Before scientists can harmonise data, they must clean it. By elim- inating the errors that arise from data entry, miscalculations, sensor malfunctions, or system glitches, scientists can build the data foundation required for harmonisation.

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Why intelligent automation is the future for regulation

pharmaphorum

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.

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VIATRIS (Mylan & Up-John Pfizer) -Openings for Regulatory Affairs Department -Apply Now

Pharma Pathway

(Merger between Mylan Laboratories & Up-John Pfizer) URGENT Opening @ VIATRIS for Regulatory Affairs- Injectables | Exp: 2-7 Years | Bangalore | Send Resumes to HR Department: Regulatory Affairs -Injectables Qualification : Masters in Pharmacy is mandatory Experience : 2 – 7 years Designation : Executive/ Assistant Manager Key responsibilities: (..)

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Considerations for safety data migration methods

European Pharmaceutical Review

Any discrepancies should be documented using a Known Difference document and the solutions or acceptance of the discrepancy are then agreed upon. Once all cases have been entered and reviewed and any discrepancies resolved, the data transfer is considered complete and a data migration summary report should be issued.

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Will AI Replace Pharma Jobs? What Experts Predict

Pharma Marketing Network

Tasks that are repetitive, data-heavy, or rules-based are most vulnerable. For example, medical data entry, pharmacovigilance documentation, and basic regulatory filing are increasingly handled by intelligent systems. Roles Most at Risk (and Why) Not all pharma jobs face equal threat from automation.