PIL Readability Testing is Mandatory in EAEU
February 15, 2022
Inpharmatis Team COVID-19 Update
We are taking all necessary measures to reduce the spread of the COVID-19 virus. The safety of our clients, partners and employees is our priority. Therefore, we have canceled all personal meetings and planned training courses. Due to the COVID-19 expansion geographically, also most GMP inspections have been suspended, traveling limited and a lot of companies begin teleworking. |
Our team is continuing to work remotely, and available in normal working hours to support you during this difficult time as best as possible. |
We value and respect our client’s business and are committed to delivering results by knowledgeable focus, meeting deadlines and professional project management despite the global COVID-19 situation. |
Our team of highly experienced experts is highly committed to supporting you during this difficult time as best as possible by continuing to provide full pharmaceutical product life-cycle management over the whole of EU & CIS in pharmacovigilance, regulatory affairs, medical writing, market access services and a range of specific software to the pharmaceutical industry. |
To maintain our client’s business continuity, we are delighted also to propose comprehensive and detailed GMP audit reports of active pharmaceutical ingredients (API) manufacturers performed by Inpharmatis. |
Schedule with us virtual meetings and find out how can we help you. Please email your request to info@inpharmatis.com or call us +371 6721 0500. |
Our CEO Dr. P.Dombure is reminding and repeatedly advising all employees, clients, and partners to practice a social distancing and take all proper hygiene steps thus reducing the risk of infection or spreading the infection to others. |
Stay strong and healthy! |
Kind regards, |
Inpharmatis team |


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