HVAC

1. Pharmaceutical HVAC Systems: An Overview
2. Air Handling Unit (AHU) Standards in the Pharmaceutical Industry
3. Standards and Types of HVAC Ductwork in the Pharmaceutical Industry
4. Standards and Types of Filters Used in the Pharmaceutical Industry HVAC System
5. Brief Overview of Pharmaceutical HVAC System and its Parts for Non classified and Classified Zones
6. Validation Protocol for Pharmaceutical HVAC System Filters: A Comprehensive Guide
7. ULPA Filters: Pure Air Quality in Pharmaceutical HVAC Systems
8. Pre-Filters Used in Pharmaceutical HVAC Systems
9. Panel Filters: An Essential Part of Pharmaceutical HVAC Systems
10. Activated Carbon Filters in HVAC Systems: A Comprehensive Guide
11. Bag Filters in Pharmaceutical HVAC Systems: A Comprehensive Guide
12. Air Changes Per Hour (ACH) in Cleanrooms: A Comprehensive Guide
13. A Comprehensive Guide to ISO 14644: Mandating Specific ACH Levels for Cleanroom Classifications
14. Procedures (SOP) for Bubble Point Test for Filters: A Comprehensive Guide
15. Procedures (SOP) for Forward Flow Test (Diffusion Test) for Filters: A Comprehensive Guide
16. Procedures (SOP) for Pressure Hold Test for Filters: A Comprehensive Guide
17. Procedures (SOP) for Water Intrusion Test for Filters: A Comprehensive Guide
18. Procedures (SOP) for Filters Integrity Test Using Aerosols: A Comprehensive Guide
19. Pharmaceutical Compressed Air and Gas Systems: An Detailed Overview
20. DQ, IQ, OQ, and PQ for Pharmaceutical Compressed Air Systems
21. Quality Requirements and Specifications for Types of Gases Used in Pharmaceutical Systems
22. Filter Selection and Related Design Considerations for Pharmaceutical Compressed Air Systems
23. Specification For Receivers, Pressure Regulators, and Condensate Traps for Pharmaceutical Compressed Air Systems
24. Distribution System Design and Specification for Pharmaceutical Compressed Air
25. Quality Criteria for Pharmaceutical Compressed Air Discharged from a Compressor
26. Pharmaceutical-Grade Oxygen (O₂): Specifications, Testing, and Procedures
27. Pharmaceutical-Grade Nitrogen (N₂): Specifications, Testing Requirements, and Procedures
28. Pharmaceutical-Grade Carbon Dioxide (CO₂): Specifications, Testing Requirements, and Procedures
29. Pharmaceutical-Grade Argon (Ar): Specifications, Testing Requirements, and Procedures
30. Pharmaceutical-Grade Helium (He): Specifications, Testing Requirements, and Procedures
31. Methods and Procedures for Determination of Moisture Content in Gases Used in the Pharmaceutical Industry
32. Standard Operating Procedure for Chilled Mirror Hygrometer to Determine Moisture Content of Pharmaceutical Gases
33. Methods and Procedures for Determination of Particulate Matter Contamination in Pharmaceutical Gases
34. Standard Operating Procedure (SOP) Determination of Residual Hydrocarbon Content in Pharmaceutical Gases
35. SOP for Air Handling Units (AHU) in the Pharmaceutical Industry
36. Types and SOP for Portable Fire Extinguishers Used in the Pharmaceutical Industry
37. Air Handling Unit and Its Working Process
38. Requirements and Maintenance of HVAC System in Manufacturing Facilities
39. Duct Designing in HVAC System
40. Difference Between HEPA and ULPA Filters
41. Checks Before and After Installation of HVAC System
42. Maintenance of Pharmaceutical Clean Area:
43. FDA Recommendation Working of a HVAC System and Its Functions
44. Buffer Area and Its Maintenance in Sterile Facility
45. Maintenance of Aseptic Conditions in Pharmaceutical Sterile Areas
46. GMP and Room Design in Pharmaceuticals
47. Essential Steps for Setting up a Pharmaceutical Cleanroom
48. New Changes in ISO 14644-1:Classification of Air Cleanliness
49. Poly Alpha Olefin (PAO) Used in HVAC Validation
50. HVAC System Validation SOP for Air Handling Unit (AHU)
51. SOP for Preventive Maintenance of AHU & Ventilation Units
52. Importance and Maintenance of Pressure Differential in Manufacturing Area
53. Role and Calculation of Air Changes per Hour in Clean Room
54. Area Types of Airlocks and Requirement in Pharmaceutical Controlled Areas
55. Sterile Area (Cleanroom) Qualification
56. Principle of Hygrometer and Its Use in Pharmaceuticals
57. Different Types of Diffusers Used in Pharmaceutical Clean Rooms (Controlled Area)
58. Heating, Ventilation and Air Conditioning (HVAC) System Validation Process
59. Prevention of Cross- contamination by HVAC