|
|
The following guideline can be ordered through the address listed in the "Source/Publisher"-category.
In cases in which you can order through the Internet we have established a hyperlink.
|
|
| SUPPLEMENTARY GUIDELINES ON GOOD MANUFACTURING PRACTICES FOR HEATING, VENTILATION AND AIR-CONDITIONING (HVAC) SYSTEMS FOR NON-STERILE DOSAGE FORMS (October 2005) |
| Internet: | http://www.who.int/entity/medicines/services/expertcommittees/pharmprep/qas048rev2hvac_withoutfigs.pdf |
| Origin/Publisher: | WHO headquarters, Avenue Appia 20, 1211 Geneva 27, Switzerland
Telephone: (+ 41 22) 791 21 11, Facsimile (fax): (+ 41 22) 791 3111, Telex: 415 416, Telegraph: UNISANTE GENEVA |
| Content: | The guideline focuses primarily on the design and GMP requirements for HVAC systems for solid
dosage form facilities. Most of the system design principles for solid dosage manufacturing facilities
will also apply other facilities such as liquids, creams and ointments. This guideline does not cover
requirements for manufacturing sites for the production of sterile products. |
| Status: | Working document QAS/02.048/Rev.2 |
|
|
|
|
|
