November 16, 2022
Published by Joachim Nuyttens at November 16, 2022
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Trevalco Academy – online training

Our brand new Trevalco Academy is now live, offering online courses in validation, quality assurance and GMP compliance for the pharmaceutical industry. Trevalco Academy is our online training center through which anyone can subscribe to and follow digital, self-paced courses. We currently have 4 online trainings to offer, including two one-day trainings: We want to offer qualitative training at a reasonable price, which is possible because this is all training material we used at clients and for training of our […]
September 30, 2022
Published by Joachim Nuyttens at September 30, 2022
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Team activity: karting

Yesterday we had a fun activity with the whole Trevalco team. We first went karting, during two sessions our colleagues could show who was the fastest, most cunning driver on the track at Inkart. Afterwards we had a nice diner together at Smokt! A good time to renew connections, tell stories of summer vacations past and get updates on each other’s project activities.
September 21, 2022
Published by Joachim Nuyttens at September 21, 2022
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What’s in the new Eudralex Annex 1

A few weeks back the new and final version of Eudralex Volume 4 Annex 1 “Manufacture of Sterile Medicinal Products” was published on the website of the European Commission. This new version will come into operation on 25 August 2023, except for point 8.123 which is postponed until 25 August 2024. Where the current version of Eudralex Volume 4 Annex 1 is 16 pages, the new version has no less than 59 pages. The new EU annex 1 regulation provides […]
September 12, 2022
Nissan Leaf bedrijfswagen
Published by Joachim Nuyttens at September 12, 2022
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Anneleen, our first electric driving colleague

At the beginning of this year Anneleen started as Trainee Consultant with Trevalco, since then she is driving with the first electric car in our fleet. We ask her whether she is happy with the car, and of course how she is liking the job. How long are you working now with Trevalco? In september 2022 that will be 8 months, starts counting right. You started almost immediately on an assignment with Pfizer in Puurs, what are you doing there […]
June 15, 2022
Published by Joachim Nuyttens at June 15, 2022
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Sustainability at Trevalco

Trevalco is an organization which treats man, environment and society with great respect. As described in our mission we want to create added value economically, ecologicaly as well as for society. It is our intent to evolve the coming years into an organization which is more mature in terms of responsible entrepreneurship. Our starting point are the sustainable development goals of the United Nations. Within Trevalco there is sufficient support, both at management level as well as at the level […]
November 24, 2021
Published by Joachim Nuyttens at November 24, 2021
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Trevalco fun day at Jesco Driving School

On November 23rd we had a little event with the whole team. We choose an activity that was both fun and useful: a full day at Jesco Driving School. We first had an interactive classroom session in which we learned about the laws of physics and dynamics, the different safety devices in our cars and about the importance of a plan B. The rest of the day was spent on the outside driving track and on the public road, all […]
November 16, 2021
Published by Joachim Nuyttens at November 16, 2021
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How to get more value from risk assessments in the life sciences industry

If you’re working in the life sciences industry you have probably been involved in risk assessments, maybe more often than you would have liked to. Whether you are working in a clinical development or pharmaceutical production environment, on drug products or medical devices, risk management has to be in place. This article will give you tips to make your risk assessments even better. One of the main reasons why risk assessments are so omnipresent is because in most cases they […]
August 30, 2021
regulations compliance
Published by Joachim Nuyttens at August 30, 2021
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Audit trail requirements on GxP computerized systems

According to Wikipedia an audit trail is a chronological record providing documentary evidence of the sequence of activities that have affected at any time a specific operation, procedure, event, or device. The first uses of audit trails date back to ancient civilizations when rudimentary methods emerged to manage goods, soldiers and financial transactions. Audit trails to ensure data integrity came into the spotlight when US regulation 21CFR Part 11 was issued in 1997. Part 11 requires the use of secure, […]
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