GMPSOP

JANUARY 29, 2025

They must follow stringent procedures to validate and maintain their information management systems for GMP compliance.For example, companies located in the USA must comply with the USFDA 21 CFR part 11 regulations. It can also directly contribute to improving the overall quality of products and services and expediting regulatory compliance.

Documentation 94

Documentation Process Improvement Pharmaceutical Manufacturing 94

European Pharmaceutical Review

AUGUST 3, 2023

The optimised framework aims to overall, drive higher product quality and improved patient safety. Summarising recommendations and best practices for CAPA process improvement, this whitepaper uses data collected from a pilot suggested in the MDIC’s initial whitepaper that proposed the framework.

Documentation 52

Documentation Process Improvement 52

Fuld & Company Blog

SEPTEMBER 20, 2023

Streamlined document review: AI-powered platforms revolutionize document reviews by automatically categorizing and analyzing vast volumes, streamlining due diligence, and potentially improving accuracy and depth.

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Documentation Process Improvement 52

Syner-G

SEPTEMBER 15, 2023

Upstream processing advancements encompass fed-batch processes , improved cell culture media, advanced feeding strategies, and tailored bioreactor control. Downstream optimization targets increased throughput, reduced costs, and improved product quality maintenance.

Drug Development 59

Drug Development Documentation Process Improvement Compounding 59

GMPSOP

MARCH 17, 2023

Additional documents included each month. record who had found the incident first time) Corrective and preventive action process Embed Code 240 SOPs, 197 GMP Manuals, 64 Templates, 30 Training modules, 167 Forms. Additional documents included each month. 240 SOPs, 197 GMP Manuals, 64 Templates, 30 Training modules, 167 Forms.

Documentation 52

Documentation Packaging Process Improvement Pharmaceutical Manufacturing 52

GMPSOP

NOVEMBER 19, 2023

You should perform product quality review annually to determine if any adjustments to product specifications, manufacturing process or raw material supply are required to improve the product further. Additional documents included each month. Trending will help identify product and process improvements. Subscribe f.

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Documentation Packaging Method Validation Process Improvement 52

The Happy PharmD

JANUARY 7, 2025

And please, leave irrelevant information off your resume. Its tempting to add extra details to stand out, but they can actually detract from the important information the hiring manager needs to see. For example, Reduced medication errors by 15% through process improvements is much more impactful than Responsible for medication safety.

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Process Improvement Documentation 52