ICH refers to The International Council for Harmonisation, which regulates the Technical Requirements for Pharmaceuticals for Human Use. The ICH was founded in 1990 with the aim to internationally harmonise the regulatory authorities and pharmaceutical industries of Europe, Japan and the United States. From its inception, the ICH has contributed to advancing public health through: Developing and … Continued
What is a temperature/humidity controlled enclosure? “Any device which provides a space in which temperature and/or humidity is controlled.
Thermal Cycling gives an indication as to how a product will react to adverse conditions, usually encountered during transportation.
What is ICH? ICH is the International Council on Harmonisation of technical requirements for Registration of Pharmaceuticals for Human Use.
If you have a requirement for ultra low storage (-80 deg), talk to Q1 Scientific today. Samples can be returned to you at controlled temperatures.
All companies developing or manufacturing pharmaceutical drugs, require a robust photostability testing process to ensure product quality and regulatory compliance. Inadequate testing can result in costly delays and lost revenue.
ANDA submission batch samples should be stored for 1 year after approval of the ANDA and samples of the drug product used for bioequivalence studies must be stored following the requirements listed in 21 CFR 320.38 and 21 CFR 320.63.
Q1 Scientific staff attended the recent training course on Stability Testing in Pharmaceutical Development and Manufacturing, held in Amsterdam on 5-6 June 2014. Topics covered included ICH guidelines, QbD, ASAP and photostability
The Q1 Scientific facility is fully supported with a back up power generator, which cuts in automatically in the event of electricity loss resulting from any ESB strike. Each environmental chamber operates independently, with separate temperature and humidity controls and all chambers are continuously monitored by a computerised monitoring system with back up alarms and … Continued
According to proposed new EU guidelines which seek to amend current Directive 2001/83/EC on Medical Devices and a Proposal for a Regulation of the European Parliament and of the Council on in vitro diagnostic medical devices, it is suggested that there will be increased requirement for evidence of stability testing medical devices. Manufacturers of Medical Devices … Continued