Use of Drug Master Files & Quality Agreements
Register for this event
- DateTue 29 September 2020
- Time8:00 AM - 2:00 PM
- LocationOnline CA National 9453
- Ticket$$ 445 per person
- Table$Price for a table per table (seats Normally between 8-12)
This combined DMF (Drug Master Files) and Quality Agreement training will discuss the advantages for suppliers and drug product manufacturers in developing these arrangements together.
Over time, there have been several misunderstandings between supplier / contractors and pharmaceutical / biologic finished product manufacturers. The root of many of the problems lie in a lack of a suitable agreement delineating roles, responsibilities and resolution to agreement to these issues. Part of these arrangements typically involve the development, support and updating of confidential technical files (Drug Master files), which allow suppliers to protect their confidential product and process information from each and every customer and share it only with the Agency.