Guidance for Industry: Microbiology Laboratories
This guideline is intended to provide general guidance on the interpretation of the PIC/S Guide to Good Manufacturing Practice for Medicinal Products (PIC/S Guide to…
Category: Pharma Industry Guidelines
FORM 483- Know more
The US Food and Drug Administration (FDA) conducts regular inspections of regulated pharmaceutical finished dose and active pharmaceutical ingredients (API) to determine whether the manufacturing…
SCHEDULE U in Pharma Manufacturing
Schedule U describes the particulars to be shown in manufacturing record. Following details are included in Schedule U: PARTICULARS TO BE SHOWN IN MANUFACTURING RECORDS…
TYPES OF AIRLOCKS USED IN PHARMA
There are three basic classifications of airlocks that are physically the same, but only the pressure cascade regime differs. Cascade Airlock:- These airlock are very…
BOOKS & STANDARDS FOR PHARMACEUTICAL INDUSTRY
HVAC DESIGN ASHRAE 62.1 Ventilation for ACC – Acceptable Indoor Air Quality ASHRAE 189 Standard for the Design of High-Performance Green Buildings ASHRAE 90.1…
DETERMINING THE EFFECTIVENESS OF THE AUTOCLAVE PROCESS
A number of tools are available to assess the performance of the autoclave; these include physical, chemical and biological indicators. It is important to note…
PHARMA. D. , MBA IN PHARMA , PhD IN PHARMA
PHARMA.D. Pharm. D. is a Latin term which means Pharmaciae doctor. Pharm. D. is a 6-year doctorate level course, including five years of scholarly examination…
BUOYANCY EFFECT CONSIDERATIONS IN THE USE OF WEIGHING BALANCE
Weighing machines are calibrated by accredited laboratories on a conventional mass basis. If the true mass of an object is to be found, or…
WEIGHTS OF DIFFERENT CLASS AS PER INTERNATIONAL ORGANIZATION OF LEGAL METROLOGY
The OIML weight classes are defined as follows: Class E1:- Weights intended to ensure traceability between national mass standards (with values derived from the…
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