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INTERNATIONAL PHARMACEUTICAL QUALITY provides in-depth coverage of emerging drug, biologic, and combination product CMC and GMP issues and developments, with a mission of helping advance quality regulatory processes globally. Headquartered in Washington, D.C., with an editorial team also based in Europe, IPQ is read by regulators, pharmacopeias, manufacturers, suppliers, consultants, lawyers, academics, and association staff around the world.
IPQ tracks the industry/regulator dialogue across a wide array of international forums – along with the developments, initiatives, regulations, guidelines, and standards in the quality regulatory arena – to create a uniquely valuable resource for the intelligence gathering, knowledge management, and communication needs of the pharmaceutical community.
Dedicated to helping its readers keep up with and influence the changes to quality regulation as it evolves to match the fast-moving process and product technologies, IPQ provides the depth and breadth of intelligence needed to form strategies, make decisions, and take the right action. The investment in an organization-wide subscription, which allows IPQ’s content to be openly shared internally, is small compared to the benefits and resource-saving potential that IPQ offers.