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October 15, 2022
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Veeda CR offers a full range of services for Phase 1, 2, 3 clinical research studies across its sites in India. Veeda's Indian clinic has been audited by the US FDA, EMEA, MHRA, ANVISA, WHO and several other agencies.
whitePaper | October 14, 2022
COVID-19 has been a catalyst for a huge amount of change across the pharmaceutical industry, acting as an accelerant for progress in its use of digital technology and prompting a reassessment.
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 | August 8, 2022
Biopharma R&D professionals generally admit that the current "high-cost, high-risk" development model is unsustainable. Despite technological.
whitePaper | February 24, 2022
The COVID-19 pandemic and resulting economic dislocation revealed long-standing vulnerabilities in our supply chains. The pandemic’s drastic impacts on demand patterns for a range of medical products including essential medicines wreaked havoc on the U.S. healthcare system.
whitePaper | December 12, 2022
To improve outcomes for cancer patients and take advantage of the groundbreaking scientific and technological progress made in oncology prevention, diagnosis, therapy
whitePaper | September 29, 2022
New biopharmaceutical drug products that alter and even save lives can be very profitable for their developers.
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