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February 4, 2019
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Caligor is a global pharmaceutical wholesaler and worldwide distributor of clinical trial supplies, fully licensed to import and export all classes of drugs, including controlled substances.
whitePaper | December 9, 2022
Randomized, double-blind clinical trials are the gold standard for adequate and well-controlled studies in modern
times. However, prior to the late 1940s, randomization and blinding were not used in medicine and as result,
bias was common.
whitePaper | July 12, 2022
As the pharmaceutical industry tries to embrace the
methodologies of quality by design (QbD) provided
by the FDA ’s process validation (PV) guidance (1) and
International Conference on Harmonization.
whitePaper | July 1, 2023
As its title implies, Annex 1 is the European guidance document for good manufacturing practices of medicinal products. As such, it serves as the road map for sterile drug manufacturers to follow in order to arrive at the pathway to the highest level of sterility, assuring that their medicinal drug products deploy operational best practices, are certifiable, and regulatorily safe.
whitePaper | April 7, 2020
The information in this document is designed to help you understand the prescription drug benefits offered under this plan and to compare these benefits to those offered by other plans. Information contained in this summary is designed to help you compare both the value and scope offormulary benefits.
whitePaper | December 22, 2022
Every viable pharmaceutical packaging system must comprise materials proven to protect its contents against moisture and other atmospheric variables, and be safe for use with the specified dosage form and the route of
whitePaper | October 7, 2022
The Drug Supply Chain Security Act is one component of the DQSA. This particular act requires the FDA to implement a national track-and-trace system by which manufacturers must affix product identifiers (barcodes) to each package of
product that is introduced into the supply chain.
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