Welcoming Birgit Hellesen

Welcoming Birgit Hellesen to Pharma IT Birgit Hellesen is a Senior Safety Data Associate with 16 years of experience from the pharmaceutical industry. Birgit’s experience spans working  with pharmacovigilance in both headquarters and affiliates and clinical trials including: Study monitoring visits, handling of SAEs in clinical trials and spontaneous reports from the market, ICSR case processing, SUSAR …

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Welcoming Louise Davidsen

Welcoming Louise Davidsen Louise Davidsen holds 13 years of experience in the pharmaceutical industry working with Clinical Trial Management mostly in the role of Clinical Trial Manager, but also in roles such as Study Coordinator and Clinical Research Associate. Louise has experience from international projects and teams, as well as with planning, running, and managing …

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Welcoming Mogens Høgh

Welcoming Seasoned IT Professional Mogens Høgh to Pharma IT Mogens Høgh is a seasoned IT professional with 35 years of experience in the IT field. He has been involved in managing projects and programmes for clients for more than 20 years in a variety of industries and sectors, but mainly in including the pharmaceutical industry …

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Pharma IT Featured in Børsen

Pharma IT was recently featured in Dansh Finance magazine Børsen where Charlotte Bech Fribert, Partner at Pharma IT, was interviewed.

Pharma IT is Nominated for the Børsen Gazelle Award

Pharma IT is Nominated for the Børsen Gazelle Award! We are very proud to have been named a Gazelle Company by business newspaper Børsen. The award is given to companies who have, as a minimum, doubled turnover or gross profits over the course of a four-year period. Since our inception in 2016, we have seen a growth …

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CMC Solutions and Pharma IT announce corporation and partnership in delivering services to the Pharma, Biotech and Medical Device Industry.

Pharma IT is a provider of drug development and IT consultants to the Pharma, Biotech and Medical Device Industry, where CMC Solutions provides consultancy services, primarily within regulatory CMC services, technical writing,  quality control, validations and project management. Both companies are based on very experienced consultants, generally with 15+ years in the pharmaceutical industry. “We …

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