GlobalCompliancePanel

Any pharmaceutical worker who must deal with products both in early and latter phases of development should attend this course in order to be aware of the regulatory requirements that will affect operations dealing with these products.

Drug safety and pharmacovigilance, Regulatory affairs, Clinical development,

Our services are aimed at benefitting the Medical Devices, Pharmaceutical, Bio Technology, Food Safety, Financial Accounting Standards, and IT Control & PCI Industries.

Regulatory requirements and recommendations from Industry Task Forces •FDA and EU requirements for software and computer system validation •FDA Inspection and Enforcement Practice How does validation help to improve your business

Validation of Methods and Processes -FDA and EU requirements for software and computer system validation

Purpose MedWatch was created with the purpose of making available a system for reporting medication errors and medical product injuries and to make the reported clinical information

Medical Device Directive (93/42/EEC) is a directive that aims to harmonize the different laws relating to the medical devices in the European Union.

Global Harmonization Task Force (GHTF) was formed in 1992 in order to achieve international harmonization in the medical devices regulation.

Pain management and existing laws have never been good friends. There are regulations and laws at state and federal levels that have attempted to regulate, organize and standardize pain management systems; however, the exceptions outnumber the rules.

Generic name is a name given to a developed drug. It is also called as international non-proprietary name and is assigned to identify the active pharmaceutical ingredients.