DATA MIGRATION

Pharmaceutical, biotechnology, and medical device manufacturers often face the challenge of migrating drug safety data between different dictionaries and computer systems, such as MedDRA, COSTART, WHODRUG, Argus ™, ARISg ™, AERS, Clintrace ™ and proprietary databases. These migrations support a variety of business needs. The licensing or acquisition of a new product from another company, implementing a new drug safety system, or unifying post-marketing and clinical safety data into one corporate system all create backlogs of adverse event cases that must be transferred.

Sentrx offers customized drug safety data migrations that utilize the unique combination of technology experts and the Safety Response Center. Sentrx evaluates the parameters of the migration project and recommends the right combination of automated and manual techniques to meet your deadlines cost-effectively.

Because Sentrx works with many different pharmacovigilance systems across our client base, we have the experience and toolset needed to attack the myriad of challenges in drug safety data migration. Let your staff focus on their daily responsibilities while Sentrx delivers the validated data you need in time for your next periodic report.