European CE Marking Process for Medical Device
“To sell medical devices in the European Union (EU), you must obtain or apply CE Marking for your product. CE Marking indicates that your medical…
“To sell medical devices in the European Union (EU), you must obtain or apply CE Marking for your product. CE Marking indicates that your medical…
“The objective of cleaning validation is to prove that the equipment is consistently cleaned of product, microbial residues, chemicals and soiling, including allergens to an…
A cosmetic is a product that is intended to be applied to the human body for cleansing, beautifying, promoting attractiveness, or altering the appearance without…
This course will provide particapants to have an opportunity to obtain advice from practicing hospital pharmacists on common management problems. It applies for hospital pharmacy…
A medical device is any instrument, apparatus, appliance, software, material or other similar or related article, intended by the manufacturer to be used, alone or…
Various people and entities are generally responsible for handling, storage and distribution. Products may be subjected to various risks at different stages in the supply…
“Good manufacturing practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize…
Warehouse management is the control of the day-to-day operations of a warehouse, such as the shipping, receiving, put-away and picking of goods. Is it the…
The Common Technical Document (CTD) is a set of specifications for an application dossier for the registration of Medicines and designed to be used across…
Unlock essential drug safety knowledge with our Pharmacovigilance Skills Training Course! This program covers monitoring and preventing adverse effects of pharmaceuticals, preparing you for a…