Friday, November 5, 2021

Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

November 4, 2021 at 10am to November 5, 2021 at 4pm – online Raw material requirements in a cGMP environment are often overlooked as a Company develops new products. Depending upon the product being developed, e.g., tablets and capsules vs. biotechnology produ… Organized by Complianceonline | Type: seminae
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions

November 4, 2021 at 10am to November 5, 2021 at 4pm – online Raw material requirements in a cGMP environment are often overlooked as a Company develops new products. Depending upon the product being developed, e.g., tablets and capsules vs. biotechnology produ… Organized by ComplianceOnline | Type: seminae
The Use of Drug Master Files & Quality Agreements

November 5, 2021 from 11am to 5pm – online 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, the… Organized by Complianceonline | Type: seminae
The Use of Drug Master Files & Quality Agreements

November 5, 2021 from 11am to 5pm – online 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, the… Organized by ComplianceOnline | Type: seminae