The F0 value of a saturated steam sterilisation process is the lethality expressed in terms of the equivalent time in minutes at a temperature of 121 °C delivered by the process to the product in its final container with reference to micro-organisms possessing a Z-value of 10. The total F0 of a process takes […]
The success of sterilization is dependent upon the performance reliability of the autoclave. Validation of effectiveness includes monitoring temperature, pressure and cycle duration time for each cycle and providing periodic sterilization/decontamination challenges (quality assurance), i.e. use of biological indicators. A logbook should be maintained to record autoclave use and be available for inspection. Temperature: This […]
Content may include the following descriptions (but not be limited to): 1. Introduction1.1 Project Description1.2 What a Validation Master Plan Is1.3 Scope of Validation Master Plan1.4 Definition for the Term Validation1.5 Validation Team Member1.6 Validation Team Responsibility 2. Concept of Qualification or Validation2.1 Fundamentals2.2 Concept of a Validation Life Cycle2.3 Elements of Validation2.4 Documentation Format […]
1. Definition of Validation Action of proving, in accordance with the principles of good manufacturing practice, that any procedure, process, equipment, material, activity, or system actually leads to the expected result Documented evidence which provides a high degree of assurance that a specific process will consistently produce a product meeting its predetermined specifications and quality […]
Interview questions mostly asked during technical round in Production : 01. Q. Which type of tablets are exempted from Disintegration testing? A. Chewable Tablets 02. Q.What are the common variables in the manufacturing of tablets?A.· Particle size of the drug substance· Bulk density of drug substance/excipients· Powder load in granulator· Amount & concentration of binder· […]
Pharmaceutical manufacturers must validate their cleaning process to ensure compliance with cGMP regulations. Minimizing equipment downtime has the potential to impact the efficiency and economics of pharmaceutical production. The main purpose of cleaning validation is to prove the effectiveness and consistency of cleaning in a given pharmaceutical production equipment to prevent cross contamination and adulteration […]
Steam Dryness: The measure of the water content of steam deliverd to the sterilizer chamber.Acceptable values are 0.9 or greater (<10% water) for non-metallic loads and 0.95 or greater (<5% water) for metallic loads. Wet steam can cause an unsterile load in two ways: Insufficient energy delivered to the load to sterilize. “wet packs”, making […]
In the pharmaceutical manufacturing and health-care industries, there are basically two types of steam–process steam and pure steam. Process steam is also known as plant steam, black steam, utility steam, boiler steam etc. Pure steam is sometimes known as clean steam. Process steam is defined as a general purpose steam whose quality is not been […]
CAPA (Corrective Action Preventive Action) and failure investigation become more and more important for the pharmaceutical industry. This becomes clear in a series of guidance documents. Above all with the ICH Q10 document, CAPA was introduced as a new quality-assuring tool. This document states e. g. that a pharmaceutical company should have a system in place […]
Technology Transfer : Receipt of product design documents from Research Center. Distribution of documents received from Research Center (RC). Checking & approval of documents generated based on RC documents i.e. Batch Manufacturing Record. Scale-up and validation of product Validation : Preparation of validation plans for facility / equipments / process including cleaning. Approval of protocols […]
