Post Views: 5,303 Job Descriptions in the pharmaceutical industry vary greatly depending on the role, but I’ll give you a clear template you can adapt for most positions (e.g., Production, Quality Assurance, Quality Control, Regulatory Affairs, R&D). Below is a…
Post Views: 4,563 QC (Quality Control) chemical testing ensures raw materials, intermediates, and finished products meet defined specifications. Adherence to Good Testing Procedures is essential for accurate, reliable, and compliant results. Below are the core principles and practices of GTP…
Post Views: 5,049 What are IPQC Instruments? IPQC (In-Process Quality Control) instruments are devices used during manufacturing to monitor and control product quality in real time.Examples: Because they directly impact product quality decisions, their qualification is mandatory under GMP. Objective…
Post Views: 3,176 Good Testing Procedure (GTP) for Microbiology – Introduction Microbiological testing ensures products, materials, and environments comply with quality, safety, and regulatory standards. A Good Testing Procedure provides systematic, controlled, and documented methods to produce reliable results. Below…
Post Views: 4,201 The User Requirements Specification describes the business needs for what users require from the system. User Requirements Specifications are written early in the validation process, typically before the system is created. They are written by the system owner…
Post Views: 4,887 A Practical Overview Stability studies in pharma are designed to show how the quality of a drug substance or product changes over time under the influence of temperature, humidity and light. The data are used to set…
Post Views: 6,937 A Critical Process Parameter (CPP) is a term used in pharmaceutical production for process variables which have an impact on a critical quality attribute (CQA) and, therefore, should be monitored or controlled to ensure the drug product obtains…
Post Views: 3,498 Every activity in Pharma have some frequencies whether it is revision of documents, qualification, validation, stability, Re-testing etc. While Acceptance criteria means numerical limits, ranges, or other criteria for tests that are used for or in making a…
Post Views: 8,002 A “media fill” (sometimes known as a “process simulation”) is the performance of an aseptic manufacturing procedure using a sterile microbiological growth medium in place of the drug solution. Dry Powder Injection Three Piece Injection Ampoules Liquid Vials
Post Views: 3,534 Miscellaneous Documents in Pharma are those documents which does not comes under any dosage form and can be applied in general.
Post Views: 15,025 Pharmaceutical formulation is the process of combining various chemical substances with the active drug to form a final medicinal product, which is called a drug mixture or drug formulation. A drug formulation can be given to the…
Post Views: 5,773 Introduction: This User Requirement Specification (URS) defines the requirements for the selection, procurement, installation, qualification, and use of chemical instruments intended for [your organization/laboratory/production facility]. The purpose of this document is to establish a clear understanding between…
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