Clean Rooms Classification as per regulatory guidelines

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This video is about Clean Rooms Classification as per regulatory guidelines • Visit our website for more stuffs like guidelines, jobs, vacancies, SOPs, Protocols, etc. • Link is : https://sites.google.com/view/pharmagyan • Let's Checkout Our Other Videos • List of ISO Guidelines : • ISO Guidelines List • Clean room classification by ISO : • Clean Room Classification | ISO Guide... • Validation of Autoclave and Qualification Part 1: • Validation of Autoclave and Qualifica... • WFI Specifications : • WFI Specifications for Pharmaceutical... • Steam Sterilization or Autoclaving Basic concepts Part 02 of 02: • Steam Sterilization or Autoclaving ... • Pharma technical series interview questions and answers : • Pharma Technical Series interview que... • Incident - • Incident in Pharmaceutical Companies|... • Deviation Part 2 of 2 - • Deviation in Pharmaceutical Companies... • Deviation Part 1 of 2 - • Deviation in Pharmaceutical Companies... • Types of Thermocouples - • Types of thermocouples used in therma... • GMP History - • GMP History| How GMP Came?| Why Follo... • GMP Vs cGMP - • GMP VS CGMP | Difference between GMP ... • Types of Validation - • Validation in hindi | validation in p... • Trick to remember 21 CFR - • Trick to remember 21 CFR in hindi | 2... • Concept of ALCOA or Data integrity - • Data integrity in Pharma companies an... • Concept of ALCOA or Data integrity - • Data Integrity in Pharmaceutical Comp... • APQR - • APQR | Annual Product Quality Review ... • CAPA - • CAPA | Corrective Action and Preventi... • Tablet manufacturing process - • Tablet manufacturing process Direct C... • • • Clean rooms are defined as especially constructed, environmentally controlled enclosed spaces with respect to airborne particulates, temperature, humidity, air pressure, air flow patterns, air motion, vibration, noise, viable (living organisms) and lighting. • • Particulate control includes: • • Particulate microbial contamination • • Particulate concentration dispersion • Clean rooms are classified in to the following types as per different guidelines: • Schedule M: Grade A, Grade B, Grade C, Grade D • USFDA (US 209E): Class 1, Class 10, Class 100, Class 1000, Class 10000, Class 100,000 • WHO 2002: Grade A, Grade B, Grade C, Grade D • EU GMP: Grade A, Grade B, Grade C, Grade D • ISO 14644-1: ISO-3, ISO-4, ISO-5, ISO-6, ISO-7, ISO-8, ISO-9 • Britain (BS 5295): Class C, Class D, Class E or F, Class G or H, Class J, Class K • Australia (AS 1386): 0.035, 0.35, 3.5, 35, 350, 3500 • Germany (VDI 2083): 1, 2, 3, 4, 5, 6 • • #PharmaGyan • Hello, Friends welcome to my channel PharmaGyan Learn about Pharmacy, Pharmaceutical companies, regulatory guidelines, Documentation procedures, SOPs, How to videos on various operating procedures, Quality Assurance, Quality control, R D, Pharmaceutical validation and qualification guidelines and procedures etc.

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