European Pharmaceutical Review

APRIL 18, 2024

When measuring active pharmaceutical ingredient (API) concentrations in effluents, the limit of quantification (LoQ) of the chosen analytical method must be sensitive enough to measure anticipated effluent concentrations or risk-derived targets at the sampling point. Another important consideration is the sampling point.

Pharmaceutical Manufacturing 86

Pharmaceutical Manufacturing Pharmaceutical Companies Pharmaceutical Companies 86

GMPSOP

DECEMBER 24, 2023

The term Good (Control) Laboratory Practice G(C)LP describes the regulations and practices concerning pharmaceutical laboratory testing as part of Good Manufacturing Practice (GMP). Understanding GLP, G(C)LP and GCP GLP : Good Laboratory Practices refer to the rules concerning testing new drugs before conducting clinical trials.

Documentation 52

Documentation Method Validation Packaging Data Entry 52

PharmaState Academy

AUGUST 9, 2023

Budget Management: Develop and manage the brand budgets, using the principles of Zero Budgeting, effectively, ensuring that resources are allocated appropriately to achieve maximise ROI. 2) Analytical Skills: Asses her ability to analyze data from prescription audit and translate these into strategies, tactics and while doing the STP.

Documentation 52

Documentation Packaging Communication 52

GMPSOP

MAY 26, 2023

The new software will have impacts on several GMP areas including the automation of product testing and release of products to market. – Estimation of resources required to bring about the change. Imagine your company is going to install new information management software in the laboratory to replace the old one.

Documentation 52

Documentation Packaging Communication Customer Service 52

GMPSOP

MAY 26, 2023

The new software will have impacts on several GMP areas including the automation of product testing and release of products to market. – Estimation of resources required to bring about the change. Imagine your company is going to install new information management software in the laboratory to replace the old one.

Documentation 52

Documentation Packaging Communication Customer Service 52

GMPSOP

JUNE 16, 2023

Importance of acceptance criteria in analytical method transfer Pharmaceuticals quality assurance & validation procedures GMPSOP Importance of acceptance criteria in analytical method transfer Last modified: June 17, 2023 Table of Contents What is analytical method transfer? Let’s dive in!

Documentation 52

Documentation Dosage Communication Method Validation 52

European Pharmaceutical Review

JANUARY 16, 2023

This also occupies a large resource, given the US Food and Drug Administration (FDA) requirement for double plate checking using a second ‘independent’ person. Cellular products directed towards personalised medicine have short manufacturing cycles, small batch sizes, demanding analytical methods, and short shelf lives.

Vaccines 128

Vaccines Research Laboratories Documentation Compounding 128