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Home
August 8, 2022
August 8, 2022
Designing a Safety and Risk Management System for Cellular Therapies
April 5, 2021
April 5, 2021
Regulatory considerations for cellular and gene therapy products in EU and US: A comparative analysis
March 9, 2021
March 9, 2021
Classification of cellular therapy and gene therapy (CGT) products: How regulators are working with industry
March 8, 2021
March 8, 2021
End-to-end pharmacovigilance support for a UK-based pharmaceutical company
APCER’s Pharmacovigilance (PV) team supported a client’s expansion into new
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March 8, 2021
March 8, 2021
Setting up Agile PV operations for a US based Pharma company
APCER’s Pharmacovigilance (PV) team helped a biotech pharmaceutical company with
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March 8, 2021
March 8, 2021
Enabling global expansion by establishing an integrated PV system
APCER helped a global pharmaceutical company in establishing a collaborative
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January 12, 2021
January 12, 2021
Importance of Engaging a Safety Partner Early in the Drug Life Cycle
Ms. Jeanne Schow, Vice President & US Head of Business
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January 10, 2021
January 10, 2021
Quality Assurance services
Our team of experienced auditors help the bio-pharma companies achieve
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January 6, 2021
January 6, 2021
APCER Factsheet
Snapshot of end-to-end Safety services offered by APCER Life Sciences.
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December 11, 2020
December 11, 2020
Advanced Therapy Medicinal Products – The Next Therapeutic Revolution
Dr. Vineet Kacker, Managing Director & Global Technical Head talks
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November 5, 2020
November 5, 2020
Human medicinal products containing nitrosamine impurities: Regulatory landscape in the United States and the European Union
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