Production

Technology Transfer in pharmaceutical manufacturing (WHO) Introduction Scope Glossary Organization and management Production: transfer (processing, packaging and cleaning) Quality control: analytical method transfer Premises and equipment Documentation Qualification and validation 1.1 Transfer of processes to an alternative site occurs at some stage in the life-cycle of most products, from development, …

Process Validation Critical Parameters Process Validation(FDA Definition) Establishing Documented Evidence, Which provides a high degree of assurance that a specific process will  consistently produce a product meeting its predetermined specifications and quality attributes.” Steps in Validating a Process: Develop validation protocol Conduct installation qualification Conduct operational qualification Conduct performance qualification …

Equipment Status log OBJECTIVE: To lay down a procedure of the maintenance of equipment sequential log. SCOPE: This SOP is applicable to all equipment and machines of all manufacturing departments RESPONSIBILITY: Production and Engineering officer/above shall be responsible to follow the procedure mentioned in this SOP. ACCOUNTABILITY : Concerned Department Head and QA Head …

Cleaning of general item OBJECTIVE: To lay down a procedure to describe the steps to be followed for cleaning general items. SCOPE: Applicable for cleaning all HDPE / SS containers, utensils, scoops, sampling tools and different cleaning aids RESPONSIBILITY: Housekeeping workers, Production Supervisors, Operators, IPQA personnel shall be responsible to follow the …

NON-CONFORMANCE RESULTS OBJECTIVE: To lay down the procedure for define the necessary action against the non-conformance of a product. SCOPE: This procedure is applicable for information, investigation and control for any kind of non- conformance noticed or confirmed in Production, Stores on in others area for its proper investigation RESPONSIBILITY: Officer – …

Prevention and Product Mix Up OBJECTIVE:   To lay down the Procedure for prevention of Product mix-up. SCOPE: This procedure is applicable for the control and prevention of product mix up during and after the manufacturing of the product . RESPONSIBILITY: QA officer and Production Officer shall be responsible for the …

SOP on housekeeping, cleaning, and sanitization of the general area in a Pharmaceutical company. Objective: To lay down a procedure for Good House Keeping, cleaning, and sanitization of the General Area. Scope: This procedure is applicable for cleaning and sanitization of General areas other than the manufacturing area of the …

Hydroxychloroquine and Antimalarial Drugs (united healthcare) These are antimalarial drugs found to induce remission in upto 50% patients of Rheumatoid Arthritis (RA), but take 3–6 months. Their advantage is relatively low toxicity, but efficacy is also low; bony erosions are not prevented. Their mechanism of action is not known, however, …

Characterization of Fine Particle in Formulation of drugs Parameters those are measured: (i) Particle size and size-distribution (ii) Shape of the particle (iii) Surface morphology of the particles (iii) Zeta potential Instrumental Methods of Particle Size Characterization: (i) Light Microscope: • First a standard graticule (BS 3625) is standardized with …

PROCESSING OF PARENTERAL PREPARATION The following steps are involved in the processing of parenteral preparation: 1. Cleaning of containers, closures, and equipment. 2. Collection of materials. 3. Preparation of parenteral products. 4. Filtration. 5. Fill the preparation in the final container. 6. Sealing the container. 7. Sterilization 8. Evaluation of …