How eCTD 4.0 implementation in Regulatory Affairs eCTD 4.0 – The electronic Common Technical Document (eCTD) is standardized guideline for…
Read More
How eCTD 4.0 implementation in Regulatory Affairs eCTD 4.0 – The electronic Common Technical Document (eCTD) is standardized guideline for…
Read MoreProduction Department in Pharmaceutical Industry Production Department-The process of Drug Manufacturing performed in Production Department in Pharmaceutical Unit into a…
Read MoreHow SAS v4 using For Bioequivalence Data analysis SAS Bioequivalence data analysis-SAS SAS is commonly employed in the analysis of…
Read MoreRegulatory response & Quality Trends for 2024 Regulatory response :ICH Q9 Quality Risk Management Regulatory response in 2023, significant changes…
Read MoreWHAT IS PHARMACEUTICAL ENGINEERING? Pharmaceutical Engineering & Designing of Drug-2024 : The origins of pharmaceuticals can be traced back to…
Read MoreLabeling and packaging in regulatory affairs? Labeling and packaging role in regulatory affairs: Labeling and packaging play a crucial role…
Read MoreWhat is Guidelines of TGA on Combination Products & Boundary 2024? TGA on Combination Products & Boundary guidelines TGA :…
Read MoreHow To Submission Of ANDA To USFDA Regulatory, 2024 ANDA Application Submitting an Abbreviated New Drug Application (ANDA) to the…
Read MoreWhat is Clinical Trials Phases in Clinical Research? clinical-trials-phase involve the examination of a new drug or treatment within a…
Read MoreWhat is Statistical-analysis-system (SAS) in Clinical SAS What-is-statistical-analysis-system (SAS)-procedures encompass prewritten programs designed to execute specific tasks. Noteworthy procedures, such…
Read More